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Psychiatric neuroimaging research in Brazil: historical overview, current challenges, and future opportunities

Abstract

The last four decades have witnessed tremendous growth in research studies applying neuroimaging methods to evaluate pathophysiological and treatment aspects of psychiatric disorders around the world. This article provides a brief history of psychiatric neuroimaging research in Brazil, including quantitative information about the growth of this field in the country over the past 20 years. Also described are the various methodologies used, the wealth of scientific questions investigated, and the strength of international collaborations established. Finally, examples of the many methodological advances that have emerged in the field of in vivo neuroimaging are provided, with discussion of the challenges faced by psychiatric research groups in Brazil, a country of limited resources, to continue incorporating such innovations to generate novel scientific data of local and global relevance.

Brain imaging; magnetic resonance; PET; SPECT; Brazil


Introduction

In the past few decades, Brazilian psychiatry research has taken a leading role among medical specialties in the country11. Martelli-Junior H, Martelli DR, Quirino IG, Oliveira MC, Lima LS, de Oliveira EA. CNPq-supported medical researchers: a comparative study of research areas. Rev Assoc Med Bras (1992). 2010;56:478-83. and achieved international recognition.22. Razzouk D, Zorzetto R, Dubugras MT, Gerolin J, Mari Jde J. Leading countries in mental health research in Latin America and the Caribbean. Braz J Psychiatry. 2007;29:118-22.

3. Gerolin J, Bressan RA, Pietrobon R, Mari Jde J. Ten-year growth in the scientific production of Brazilian psychiatry: the impact of the new evaluation policies. Braz J Psychiatry. 2010;32:6-10.
-44. Moreira-Almeida A, E Oliveira FH. A brief panorama of Brazil's contributions to psychiatry. Int Rev Psychiatry. 2017;29:206-7. Since it was first introduced in the 1990s, psychiatric neuroimaging research has made important contributions to such growth, and is now established as a major field of neuroscientific investigation in psychiatry in Brazil.

Methodological advances relating to in vivo neuroimaging continuously emerge, and it is essential to incorporate such innovations to studies investigating questions of relevance to psychiatry. From that perspective, the present article provides a historical overview of psychiatric neuroimaging research in Brazil, followed by a discussion of the challenges and opportunities that lie ahead.

The concept of neuroimaging as a subspecialty in psychiatric research and the establishment of psychiatric neuroimaging research teams

Over the past 40 years, a growing number of studies worldwide have applied neuroimaging methods to evaluate pathophysiological and treatment aspects of psychiatric disorders.55. Kotrla KJ, Weinberger DR. Brain imaging in schizophrenia. Annu Rev Med. 1995;46:113-22.,66. Silbersweig DA, Rauch SL. Neuroimaging in psychiatry: a quarter century of progress. Harv Rev Psychiatry. 2017;25:195-7. First, the field has benefited from its access to mainstream neuroradiological techniques, including structural magnetic resonance imaging (MRI), which is used to evaluate brain volumes and macroscopic lesions,77. Pearlson GD, Calhoun V. Structural and functional magnetic resonance imaging in psychiatric disorders. Can J Psychiatry. 2007;52:158-66. as well as positron emission tomography (PET) and single-photon emission computed tomography (SPECT), which are used for the assessment of brain metabolism with 18F-fluorodeoxyglucose (18F-FDG PET) and regional cerebral blood flow (rCBF SPECT) respectively.88. Ingvar DH. History of brain imaging in psychiatry. Dement Geriatr Cogn Disord. 1997;8:66-72.,99. Raichle ME. A brief history of human brain mapping. Trends Neurosci. 2009;32:118-26. Moreover, leading research institutions worldwide have also gained access to increasingly more sophisticated imaging methods for dynamic brain activity mapping during cognitive, emotion-provoking, or motor tasks using functional MRI (fMRI),77. Pearlson GD, Calhoun V. Structural and functional magnetic resonance imaging in psychiatric disorders. Can J Psychiatry. 2007;52:158-66. and to molecular imaging using PET, SPECT, and magnetic resonance spectroscopy (MRS).88. Ingvar DH. History of brain imaging in psychiatry. Dement Geriatr Cogn Disord. 1997;8:66-72.,1010. Malhi GS, Valenzuela M, Wen W, Sachdev P. Magnetic resonance spectroscopy and its applications in psychiatry. Aust N Z J Psychiatry. 2002;36:31-43. Although routine diagnostic applications of neuroradiological methods in clinical psychiatry have not yet emerged (a topic that is outside the scope of this article), brain imaging has become an essential field of psychiatry research.

In addition to the usual methodological planning associated with scientific investigation (i.e., study design, power calculations, definition of criteria for sample recruitment, choice of symptom assessment scales, etc.), neuroimaging research involves 1) choosing suitable equipment and defining strict protocols for data acquisition, quality control, and storage; 2) preprocessing routines using computational methods (for instance, removal of extracerebral tissue from structural MRI datasets and image inhomogeneity correction); 3) image processing steps, such as spatial normalization of datasets to anatomical templates, smoothing, correction for partial volume effects (in the case of PET or SPECT datasets), among others; 4) extraction of quantitative indices from images, such as regional brain volumes (in case of structural MRI), quantification of interregional correlations and anticorrelations (in case of connectivity investigations using fMRI), etc.; and finally, 5) applying contemporary, well-validated statistical approaches for data inference at both the individual and group levels.1111. Lindquist MA. The statistical analysis of fMRI data. Statist Sci. 2008;23:439-64.

Following the steps described above, two main paths have been used by researchers worldwide in their efforts to generate relevant, novel data from neuroimaging investigations in psychiatry, both of which are being applied not only in large academic health centers, but also in specialized research institutes dedicated to the study of brain disorders. In the first of these two models, knowledgeable clinical research groups interested in questions pertaining to a specific area of psychiatry (e.g., mood or anxiety disorders, psychosis, etc.) use their expertise to devise original hypotheses that are best testable with neuroimaging methods. To achieve their goals, such psychiatric research groups typically liaise with teams of imaging experts from the same or other academic environments (neuroradiologists, physicists, and nuclear medicine physicians).1212. UMGC: Nuclear Medicine and Molecular Imaging [Internet]. 2019 [cited 2019 Oct 03]. www.umcg.nl/EN/corporate/Departments/NGMB/research/research_topics/Paginas/default.aspx
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,1313. The University of British Columbia. Faculty of Medicine, Department of Radiology. Neurosciences Program [Internet]. 2019 [cited Oct 03]. https://radiology.med.ubc.ca/research/neurosciences-program/
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In the second model, psychiatrists, psychologists, and other mental health professionals develop a deeper and broader interest in neuroimaging research, and they themselves establish specialized groups dedicated to brain imaging.1414. Johns Hopkins Medicine, Division of Prychiatric Neuroimaging. Psychiatry and behavioral sciences [Internet]. 2019 [cited 2019 Oct 03]. www.hopkinsmedicine.org/psychiatry/research/neuroimaging/
www.hopkinsmedicine.org/psychiatry/resea...

15. Harvard Medical School, Psychiatry Neuroimaging Laboratory (PNL). Leanding the way to brain discorvery [Internet]. 2019 [cited 2019 Oct 03]. http://www.pnl.bwh.harvard.edu/
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-1616. Phillips Neuroimaging Studies. Mood and brain lab [Internet]. 2019 [cited 2019 Oct 03]. http://www.phillips.pitt.edu/index.htm
http://www.phillips.pitt.edu/index.htm...
Most of these psychiatric neuroimaging research groups worldwide have focused on the systematic investigation of a few disorders of interest, while a minority has explored psychiatry more broadly. Close and fruitful collaboration with neuroradiology experts, physicists, radiopharmacists, and other imaging professionals is still crucial in this model to ensure access to imaging equipment and state-of-the-art methods for acquisition of brain data; however, study design, appropriate selection of data acquisition and image processing methods for the specific questions being asked, and interpretation of research results in light of previous neuroimaging knowledge that cuts across boundaries of different fields of psychiatry are typically reserved for the group of mental health researchers. In Brazil, there have been a few such initiatives to date, which will be described in the next section of this article.

Whichever of these two paths is chosen, the inclusion of computer scientists in the teams is absolutely essential, either as full-time investigators hired to work specifically in the psychiatric neuroimaging lab or as collaborators based in external academic computer science departments. Such professionals master the use of the software suites most commonly used in brain image processing (several of which are available as freeware but relatively complex), implement the information technology infrastructure necessary to run such software, propose innovative image analysis methods, and provide support to psychiatrists and other mental health researchers after they have been trained to use software to process data from their own studies. It should be noted that the wealth of neuroimaging research applications has driven the establishment of entire computer science groups or departments entirely devoted to this field in academic institutions.1717. Perelman School of Medicine University Pennsylvania. Section for biomedical image analysis (SBIA) [Internet]. 2019 [cited 2019 Oct 03]. http://www.med.upenn.edu/sbia/
http://www.med.upenn.edu/sbia/...

A concise history of psychiatric neuroimaging research in Brazil and its impact

During the late 1980s and 1990s, a number of Brazilian psychiatrists working abroad led the development of several quantitative, controlled psychiatric neuroimaging investigations using computed tomography,1818. Hübner CV, Gattaz WF. [Cerebral Computed Tomography and Schizophrenia: A Critical Review of the Literature]. Arq Neuropsiquiatr. 1988;46:320-9.,1919. Dalgalarrondo P, Gattaz WF. Basal ganglia abnormalities in tardive dyskinesia. Possible relationship with duration of neuroleptic treatment. Eur Arch Psychiatry Clin Neurosci. 1994;244:272-7. structural MRI,2020. Elkis H, Friedman L, Wise A, Meltzer HY. Meta-analyses of studies of ventricular enlargement and cortical sulcal prominence in mood disorders. Comparisons with controls or patients with schizophrenia. Arch Gen Psychiatry. 1995;52:735-46. rCBF SPECT,2121. Zilbovicius M, Garreau B, Samson Y, Remy P, Barthélémy C, Syrota A, et. al. Delayed maturation of the frontal cortex in childhood autism. Am J Psychiatry. 1995;152:248-52.,2222. Busatto GF, Costa DC, Ell PJ, Pilowsky LS, David AS, Kerwin RW. Regional cerebral blood flow (rCBF) in schizophrenia during verbal memory activation: a 99mTc-HMPAO single photon emission tomography (SPET) study. Psychol Med. 1994;24:463-72. task-related fMRI,2323. Busatto G, Howard RJ, Ha Y, Brammer M, Wright I, Woodruff PW, et al. A functional magnetic resonance imaging study of episodic memory. Neuroreport. 1997;8:2671-5. and molecular imaging with SPECT.2424. Busatto GF, Pilowsky LS, Costa DC, Ell PJ, David AS, Lucey JV, et al. Correlation between reduced in vivo benzodiazepine receptor binding and severity of psychotic symptoms in schizophrenia. Am J Psychiatry. 1997;154:56-63. Erratum in: Am J Psychiatry 1997;154:722.,2525. Kapczinski F, Quevedo J, Curran HV, Fleminger S, Toone B, Cluckie A, et al. Brain uptake of iomazenil in cirrhotic patients: a single photon emission tomography study. J Psychopharmacol. 1999;13:219-25.

In regard to controlled studies carried out entirely in Brazil involving samples affected by psychiatric disorders, the first quantitative neuroimaging publications in international peer-reviewed journals date from the early 2000s (Figure 1).2626. Busatto GF, Zamignani DR, Buchpiguel CA, Garrido GE, Glabus MF, Rocha ET, et al. A voxel-based investigation of regional cerebral blood flow abnormalities in obsessive-compulsive disorder using single photon emission computed tomography (SPECT). Psychiatry Res. 2000;99:15-27.

27. Busatto GF, Buchpiguel CA, Zamignani DR, Garrido GE, Glabus MF, Rosario-Campos MC, et al. Regional cerebral blood flow abnormalities in early-onset obsessive-compulsive disorder: an exploratory SPECT study. J Am Acad Child Adolesc Psychiatry. 2001;40:347-54.

28. Skaf CR, Yamada A, Garrido GE, Buchpiguel CA, Akamine S, Castro CC, et al. Psychotic symptoms in major depressive disorder are associated with reduced regional cerebral blood flow in the subgenual anterior cingulate cortex: a voxel-based single photon emission computed tomography (SPECT) study. J Affect Disord. 2002;68:295-305.
-2929. Garrido GE, Furuie SS, Buchpiguel CA, Bottino CM, Almeida OP, Cid CG, et al. Relation between medial temporal atrophy and functional brain activity during memory processing in Alzheimer's disease: a combined MRI and SPECT study. J Neurol Neurosurg Psychiatry. 2002;73:508-16. These papers reported the findings of studies carried out at the Laboratory of Psychiatric Neuroimaging housed in the Clinics Hospital, University of São Paulo Medical School (HCFMUSP), set up in 1997. Supported by a state funding agency (Fundação de Amparo à Pesquisa do Estado de São Paulo, FAPESP), this laboratory was established by the Institute of Psychiatry at HCFMUSP (IPq-HCFMUSP) in partnership with the nuclear medicine division and the neuroradiology research group at the HCFMUSP Institute of Radiology (InRad-HCFMUSP).3030. Busatto Filho G. Estudo de alterações do funcionamento cerebral regional em distúrbios neuro-psiquiátricos utilizando tomografia computadorizada por emissão de fótons (SPET) [Internet]. 2019 [cited 2019 Oct 03]. http://www.bv.fapesp.br/pt/auxilios/3222/estudo-de-alteracoes-do-funcionamento-cerebral-regional-em-disturbios-neuro-psiquiatricos-utilizando/
http://www.bv.fapesp.br/pt/auxilios/3222...
In 2003, the Laboratory of Psychiatric Neuroimaging was incorporated as one of the 62 official facilities participating in the HCFMUSP network of Laboratories of Medical Investigation (LIM 21), and has since performed its activities following the second model described in the previous section of this article (Figure 2A for number of publications from 2000 to the present date). Table 1 shows how LIM 21 uses MRI, PET, and SPECT technologies to investigate pathophysiological and treatment aspects of several psychiatric conditions. Such broadness stemmed from a vision that, given the large size of the University of São Paulo (USP), a lab dedicated to a subspecialty of key relevance to psychiatry should not be limited to support research performed by the laboratory’s leaders, but rather should serve as a platform for collaborations with other research groups. Additionally, it should be noted that other leaders at IPq-HCFMUSP have coordinated neuroimaging research initiatives independently from LIM 21 in areas of MRS applied to mood disorders and psychosis,3131. Yacubian J, de Castro CC, Ometto M, Barbosa E, de Camargo CP, Tavares H, et al. 31P-spectroscopy of frontal lobe in schizophrenia: alterations in phospholipid and high-energy phosphate metabolism. Schizophr Res. 2002;58:117-22.

32. Amaral JA, Tamada RS, Issler CK, Caetano SC, Cerri GG, de Castro CC, et al. A 1HMRS study of the anterior cingulate gyrus in euthymic bipolar patients. Hum Psychopharmacol. 2006;21:215-20.

33. Soeiro-de-Souza MG, Salvadore G, Moreno RA, Otaduy MC, Chaim KT, Gattaz WF, et al. Bcl-2 rs956572 polymorphism is associated with increased anterior cingulate cortical glutamate in euthymic bipolar I disorder. Neuropsychopharmacology. 2013;38:468-75.
-3434. Machado-Vieira R, Zanetti MV, Otaduy MC, De Sousa RT, Soeiro-de-Souza MG, Costa AC, et al. Increased brain lactate during depressive episodes and reversal effects by lithium monotherapy in drug-naive bipolar disorder: a 3-T 1H-MRS study. J Clin Psychopharmacol. 2017;37:40-5. morphometric MRI in mood disorders, obsessive-compulsive disorder, and psychosis,3535. Gregório SP, Sallet PC, Do KA, Lin E, Gattaz WF, Dias-Neto E. Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: preliminary evidence. Psychiatry Res. 2009;165:1-9.

36. Soeiro-de-Souza MG, Lafer B, Moreno RA, Nery FG, Chile T, Chaim K, et al. The CACNA1C risk allele rs1006737 is associated with age-related prefrontal cortical thinning in bipolar I disorder. Transl Psychiatry. 2017;7:e1086.
-3737. Vattimo EF, Barros VB, Requena G, Sato JR, Fatori D, Miguel EC, et al. Caudate volume differences among treatment responders, non-responders and controls in children with obsessive-compulsive disorder. Eur Child Adolesc Psychiatry. 2019;28:1607-17. functional imaging studies in obsessive-compulsive disorder,3838. Castillo AR, Buchpiguel CA, de Araújo LA, Castillo JC, Asbahr FR, Maia AK, et al. Brain SPECT imaging in children and adolescents with obsessive-compulsive disorder. J Neural Transm (Vienna). 2005;112:1115-29.

39. Hoexter MQ, Biazoli CE Jr, Alvarenga PG, Batistuzzo MC, Salum GA, Gadelha A, et al. Low frequency fluctuation of brain spontaneous activity and obsessive-compulsive symptoms in a large school-age sample. J Psychiatr Res. 2018;96:224-30.
-4040. Batistuzzo MC, Balardin JB, Martin Mda G, Hoexter MQ, Bernardes ET, Borcato S, et al. Reduced prefrontal activation in pediatric patients with obsessive-compulsive disorder during verbal episodic memory encoding. J Am Acad Child Adolesc Psychiatry. 2015;54:849-58. and psychiatric manifestations of neurological disorders.4141. Marchetti RL, Azevedo D Jr, de Campos Bottino CM, Kurcgant D, de Fátima Horvath Marques A, Marie SK, et al. Volumetric evidence of a left laterality effect in epileptic psychosis. Epilepsy Behav. 2003;4:234-40.

42. Cardoso EF, Maia FM, Fregni F, Myczkowski ML, Melo LM, Sato JR, et al. Depression in Parkinson's disease: convergence from voxel-based morphometry and functional magnetic resonance imaging in the limbic thalamus. Neuroimage. 2009;47:467-72.
-4343. Terroni L, Amaro E Jr, Iosifescu DV, Mattos P, Yamamoto FI, Tinone G, et al. The association of post-stroke anhedonia with salivary cortisol levels and stroke lesion in hippocampal/parahippocampal region. Neuropsychiatr Dis Treat. 2015;11:233-42.

Figure 1
Geographic distribution of research groups conducting psychiatric neuroimaging studies in public and private institutions in several Brazilian states. The fields of interest of each group are listed in Table 1.
Figure 2
A) Total number of PubMed neuroimaging papers related to psychiatry published from the year 2000 onwards with participation of researchers based in all centers in Brazil (dotted line) and specifically Laboratory of Psychiatric Neuroimaging (LIM 21) at HCFMUSP (solid line), which contributed to 29.5% of the overall articles published to date. Details for the types of publications are provided in Table 2. The methods used to select publications (up until September 2019) are outlined in the online-only supplementary material. Neuroimaging papers published when researchers were working as members of research groups based in other countries were excluded, as were nonneuroimaging papers. B) Yearly number of papers published in the fields of psychiatry or neuroscience in journals with the highest impact factors (IF) (greater than 6, as calculated by Clarivate Analytics) by Brazilian groups (dotted line) and specifically by LIM 21 at the HCFMUSP (solid line). Journals were as follows: American Journal of Psychiatry (n=10); Biological Psychiatry (n=7); British Journal of Psychiatry (n=3); Cerebral Cortex (n=4); JAMA Psychiatry (formerly known as Archives of General Psychiatry) (n=6); Journal of Neurology, Neurosurgery and Psychiatry (n=1); Journal of Neuroscience (n=2); Lancet Psychiatry (n=1); Molecular Psychiatry (n=4); Neuropsychopharmacology (n=10); Neuroscience and Biobehavioural Reviews (n=6); and Schizophrenia Bulletin (n=3).
Table 1
Distribution of psychiatric neuroimaging publications by Brazilian research groups using different modalities from the year 2000 onwards

A specialized psychiatric neuroimaging lab was also set up at the Federal University of São Paulo (UNIFESP) in 2004, with support from FAPESP and other funding agencies. Since then, this group has conducted a significant number of SPECT and MRI studies evaluating samples of patients with psychiatric conditions including psychosis,4444. Zugman A, Pedrini M, Gadelha A, Kempton MJ, Noto CS, Mansur RB, et al. Serum brain-derived neurotrophic factor and cortical thickness are differently related in patients with schizophrenia and controls. Psychiatry Res. 2015;234:84-9.,4545. Leme IB, Gadelha A, Sato JR, Ota VK, Mari JJ, Melaragno MI, et al. Is there an association between cortical thickness, age of onset, and duration of illness in schizophrenia? CNS Spectr. 2013;18:315-21. mood disorders,4646. Baldaçara L, Nery-Fernandes F, Rocha M, Quarantini LC, Rocha GG, Guimarães JL, et al. Is cerebellar volume related to bipolar disorder? J Affect Disord. 2011;135:305-9. post-traumatic stress disorder (PTSD),4747. Baldaçara L, Zugman A, Araújo C, Cogo-Moreira H, Lacerda AL, Schoedl A, et al. Reduction of anterior cingulate in adults with urban violence-related PTSD. J Affect Disord. 2014;168:13-20.,4848. Baldaçara L, Jackowski AP, Schoedl A, Pupo M, Andreoli SB, Mello MF, et al. Reduced cerebellar left hemisphere and vermal volume in adults with PTSD from a community sample. J Psychiatr Res. 2011;45:1627-33. personality disorders,4949. Araujo TB, Araujo Filho GM, Sato JR, de Araújo CM, Lisondo CM, Carrete H Jr, et al. Cortical morphology changes in women with borderline personality disorder: a multimodal approach. Braz J Psychiatry. 2014;36:32-8. and neuropsychiatric features associated with Parkinson’s disease,5050. Moriyama TS, Felicio AC, Chagas MH, Tardelli VS, Ferraz HB, Tumas V, et al. Increased dopamine transporter density in Parkinson's disease patients with social anxiety disorder. J Neurol Sci. 2011;310:53-7.,5151. Felicio AC, Moriyama TS, Godeiro-Junior C, Shih MC, Hoexter MQ, Borges V, et al. Higher dopamine transporter density in Parkinson's disease patients with depression. Psychopharmacology (Berl). 2010;211:27-31. as well as more recently leading large-scale studies of childhood/adolescent brain development (Table 1).5252. Moura LM, Crossley NA, Zugman A, Pan PM, Gadelha A, Del Aquilla MA, et al. Coordinated brain development: exploring the synchrony between changes in grey and white matter during childhood maturation. Brain Imaging Behav. 2017;11:808-17.

53. Pan PM, Sato JR, Salum GA, Rohde LA, Gadelha A, Zugman A, et al. Ventral striatum functional connectivity as a predictor of adolescent depressive disorder in a longitudinal community-based sample. Am J Psychiatry. 2017;174:1112-9.
-5454. Moura LM, Kempton M, Barker G, Salum G, Gadelha A, Pan PM, et al. Age-effects in white matter using associated diffusion tensor imaging and magnetization transfer ratio during late childhood and early adolescence. Magn Reson Imaging. 2016;34:529-34. This group is a branch of the Interdisciplinary Laboratory of Clinical Neuroscience (LiNC), a broader neuroscience initiative at UNIFESP devoted to the application of neuroscientific techniques in psychiatric research. This effort has provided impetus to a number of innovative neuroimaging studies at the interface with other neuroscience areas, mainly molecular genetics.5555. Ota VK, Bellucco FT, Gadelha A, Santoro ML, Noto C, Christofolini DM, et al. PRODH polymorphisms, cortical volumes and thickness in schizophrenia. PLoS One. 2014;9:e87686.

At the Department of Neuroscience and Behavioral Sciences at USP’s Medical School at Ribeirão Preto (FMRP-USP), current leaders in psychiatry were trained in neuroimaging research during their doctoral studies5656. Crippa JA, Zuardi AW, Busatto GF, Sanches RF, Santos AC, Araújo D, et al. Cavum septum pellucidum and adhesio interthalamica in schizophrenia: an MRI study. Eur Psychiatry. 2006;21:291-9. and as postdoctoral fellows in Brazil5757. Crippa JA, Zuardi AW, Garrido GE, Wichert-Ana L, Guarnieri R, Ferrari L, et al. Effects of cannabidiol (CBD) on regional cerebral blood flow. Neuropsychopharmacology. 2004;29:417-26. or abroad.5858. Del-Ben CM, Deakin JF, McKie S, Delvai NA, Williams SR, Elliott R, et al. The effect of citalopram pretreatment on neuronal responses to neuropsychological tasks in normal volunteers: an FMRI study. Neuropsychopharmacology. 2005;30:1724-34.,5959. Fusar-Poli P, Crippa JA, Bhattacharyya S, Borgwardt SJ, Allen P, Martin-Santos R, et al. Distinct effects of {delta}9-tetrahydrocannabinol and cannabidiol on neural activation during emotional processing. Arch Gen Psychiatry. 2009;66:95-105. With links to the local Center of Imaging Sciences and Medical Physics at FMRP-USP, this multidisciplinary team has since conducted neuroimaging investigations, with leadership in the following topics: frequency and clinical correlates of neurodevelopmental markers in neuropsychiatric disorders6060. Crippa JA, Uchida R, Busatto GF, Guimarães FS, Del-Ben CM, Zuardi AW, et al. The size and prevalence of the cavum septum pellucidum are normal in subjects with panic disorder. Braz J Med Biol Res. 2004;37:371-4.; MRI studies in anxiety disorders6161. Uchida RR, Del-Ben CM, Busatto GF, Duran FL, Guimarães FS, Crippa JA, et al. Regional gray matter abnormalities in panic disorder: a voxel-based morphometry study. Psychiatry Res. 2008;163:21-9.

62. Linares IM, Jackowski AP, Trzesniak CM, Arrais KC, Chagas MH, Sato JR, et al. Cortical thinning of the right anterior cingulate cortex in spider phobia: a magnetic resonance imaging and spectroscopy study. Brain Res. 2014;1576:35-42.
-6363. Machado-de-Sousa JP, Osório FL, Jackowski AP, Bressan RA, Chagas MH, Torro-Alves N, et al. Increased amygdalar and hippocampal volumes in young adults with social anxiety. PLoS One. 2014;9:e88523. and postpartum depression6464. Rosa CE, Soares JC, Figueiredo FP, Cavalli RC, Barbieri MA, Schaufelberger MS, et al. Glutamatergic and neural dysfunction in postpartum depression using magnetic resonance spectroscopy. Psychiatry Res Neuroimaging. 2017;265:18-25.,6565. Rezende MG, Rosa CE, Garcia-Leal C, Figueiredo FP, Cavalli RC, Bettiol H, et al. Correlations between changes in the hypothalamic-pituitary-adrenal axis and neurochemistry of the anterior cingulate gyrus in postpartum depression. J Affect Disord. 2018;239:274-81.; neuropsychiatric features associated with neurological disorders6666. Guarnieri R, Wichert-Ana L, Hallak JE, Velasco TR, Walz R, Kato M, et al. Interictal SPECT in patients with mesial temporal lobe epilepsy and psychosis: a case-control study. Psychiatry Res. 2005;138:75-84.,6767. Chagas MH, Tumas V, Pena-Pereira MA, Machado-de-Sousa JP, Dos Santos AC, Sanches RF, et al. Neuroimaging of major depression in Parkinson's disease: Cortical thickness, cortical and subcortical volume, and spectroscopy findings. J Psychiatr Res. 2017;90:40-5.; and pharmacological studies evaluating brain functional and structural imaging correlates of the use of cannabinoids6868. Crippa JA, Derenusson GN, Ferrari TB, Wichert-Ana L, Duran FL, Martin-Santos R, et al. Neural basis of anxiolytic effects of cannabidiol (CBD) in generalized social anxiety disorder: a preliminary report. J Psychopharmacol. 2011;25:121-30. and a number of other drugs (Table 1).6969. Del-Ben CM, Ferreira CA, Sanchez TA, Alves-Neto WC, Guapo VG, de Araujo DB, et al. Effects of diazepam on BOLD activation during the processing of aversive faces. J Psychopharmacol. 2012;26:443-51.,7070. Chaves C, Marque CR, Maia-de-Oliveira JP, Wichert-Ana L, Ferrari TB, Santos AC, et al. Effects of minocycline add-on treatment on brain morphometry and cerebral perfusion in recent-onset schizophrenia. Schizophr Res. 2015;161:439-45.

Still in São Paulo, computer scientists and research associates founded the Center for Cognition and Complex Systems (NCSC) at the ABC Federal University (UFABC) in 2009. This prolific computer science group focuses almost entirely on innovative image processing and statistical methods applied to the analysis of neuroimaging data across several fields of interest to psychiatry (Table 1), working in collaboration with clinical psychiatrists from other Brazilian centers.7171. Sato JR, Biazoli CE Jr, Salum GA, Gadelha A, Crossley N, Vieira G, et al. Association between abnormal brain functional connectivity in children and psychopathology: a study based on graph theory and machine learning. World J Biol Psychiatry. 2018;19:119-29.

72. Trambaiolli LR, Biazoli CE Jr, Balardin JB, Hoexter MQ, Sato JR. The relevance of feature selection methods to the classification of obsessive-compulsive disorder based on volumetric measures. J Affect Disord. 2017;222:49-56.

73. Rebello K, Moura LM, Xavier G, Spindola LM, Carvalho CM, Hoexter MQ, et al. Association between spontaneous activity of the default mode network hubs and leukocyte telomere length in late childhood and early adolescence. J Psychosom Res. 2019;127:109864.
-7474. Sato JR, Hoexter MQ, Oliveira PP Jr, Brammer MJ, MRC AIMS Consortium, Murphy D, et al. Inter-regional cortical thickness correlations are associated with autistic symptoms: a machine-learning approach. J Psychiatr Res. 2013;47:453-9.

Outside São Paulo, scientists based at the Federal University of Minas Gerais (UFMG) Department of Mental Health led the establishment of a PET imaging lab – the main facility at the National Institute of Molecular Medicine funded by the National Research and Technology Council (Conselho Nacional de Desenvolvimento Científico e Tecnológico, CNPq) in the context of the Brazilian National Institutes of Science and Health (Institutos Nacionais de Ciência e Tecnologia) in 2008. This team has since conducted a number of 18F-FDG PET studies,7575. Schütze M, Costa DS, Paula JJ, Malloy-Diniz LF, Malamut C, Mamede M, et al. Use of machine learning to predict cognitive performance based on brain metabolism in Neurofibromatosis type 1. PLoS One. 2018;13:e0203520.,7676. Schütze M, Romanelli LC, Rosa DV, Carneiro-Proietti AB, Nicolato R, Romano-Silva MA, et al. Brain metabolism changes in patients infected with HTLV-1. Front Mol Neurosci. 2017;10:52. as well as structural MRI investigations of bipolar disorders in collaboration with LIM 21 in São Paulo (Table 1).7777. Neves MC, Albuquerque MR, Malloy-Diniz L, Nicolato R, Neves FS, Souza-Duran FL, et al. A voxel-based morphometry study of gray matter correlates of facial emotion recognition in bipolar disorder. Psychiatry Res. 2015;233:158-64.,7878. Duarte DG, Neves Mde C, Albuquerque MR, de Souza-Duran FL, Busatto G, Corrêa H. Gray matter brain volumes in childhood-maltreated patients with bipolar disorder type I: a voxel-based morphometric study. J Affect Disord. 2016;197:74-80.

In the state of Rio Grande do Sul, knowledgeable clinical and basic science research groups based at the Federal University of Rio Grande do Sul (UFRGS) and the Pontifical Catholic University (PUC) have adopted the first model outlined in the previous section of this article, testing original hypotheses in a number of psychiatric neuroimaging studies carried out in collaboration with teams of imaging experts either from the local Clinics Hospital of Porto Alegre (HCPA), the PUC-based Brain Institute (InsCer), or São Paulo-based centers. These groups have contributed to the development of the field of psychiatric neuroimaging in Brazil by leading studies on attention-deficit/hyperactivity disorder (ADHD),7979. Picon FA, Sato JR, Anés M, Vedolin LM, Mazzola AA, Valentini BB, et al. Methylphenidate alters functional connectivity of default mode network in drug-naive male adults with ADHD. J Atten Disord. 2020;24:447-55.

80. Silva N Jr, Szobot CM, Shih MC, Hoexter MQ, Anselmi CE, Pechansky F, et al. Searching for a neurobiological basis for self-medication theory in ADHD comorbid with substance use disorders: an in vivo study of dopamine transporters using (99m)Tc-TRODAT-1 SPECT. Clin Nucl Med. 2014;39:e129-34.
-8181. de Oliveira Rosa V, Franco AR, Salum Júnior GA, Moreira-Maia CR, Wagner F, Simioni A, et al. Effects of computerized cognitive training as add-on treatment to stimulants in ADHD: a pilot fMRI study. Brain Imaging Behav. 2019 Jun 19[Online ahead of print] child and adolescent development,8282. Axelrud LK, Santoro ML, Pine DS, Talarico F, Gadelha A, Manfro GG, et al. Polygenic risk score for Alzheimer's disease: implications for memory performance and hippocampal volumes in early life. Am J Psychiatry. 2018;175:555-63.,8383. Miguel PM, Pereira LO, Barth B, de Mendonça Filho EJ, Pokhvisneva I, Nguyen TT, et al. Prefrontal cortex dopamine transporter gene network moderates the effect of perinatal hypoxic-ischemic conditions on cognitive flexibility and brain gray matter density in children. Biol Psychiatry. 2019;86:621-30. psychosis,8484. Czepielewski LS, Massuda R, Panizzutti B, Grun LK, Barbé-Tuana FM, Teixeira AL, et al. Telomere Length and CCL11 Levels are associated with gray matter volume and episodic memory performance in schizophrenia: evidence of pathological accelerated aging. Schizophr Bull. 2018;44:158-67. mood and anxiety disorders,8585. Duarte JA, Massuda R, Goi PD, Vianna-Sulzbach M, Colombo R, Kapczinski F, et al. White matter volume is decreased in bipolar disorder at early and late stages. Trends Psychiatry Psychother. 2018;40:277-84.

86. Toazza R, Franco AR, Buchweitz A, Molle RD, Rodrigues DM, Reis RS, et al. Amygdala-based intrinsic functional connectivity and anxiety disorders in adolescents and young adults. Psychiatry Res Neuroimaging. 2016;257:11-6.
-8787. Sartori JM, Reckziegel R, Passos IC, Czepielewski LS, Fijtman A, Sodré LA, et al. Volumetric brain magnetic resonance imaging predicts functioning in bipolar disorder: a machine learning approach. J Psychiatr Res. 2018;103:237-43. and autism (Table 1).8888. Heinsfeld AS, Franco AR, Craddock RC, Buchweitz A, Meneguzzi F. Identification of autism spectrum disorder using deep learning and the ABIDE dataset. Neuroimage Clin. 2017;17:16-23.

The same collaborative model has been applied by research groups based at other universities in Brazil. In the state of Rio de Janeiro, notably, psychiatrists based at the Federal University of Rio de Janeiro (UFRJ) have been involved in a number of original MRI studies on psychiatric disorders including PTSD,8989. Rocha-Rego V, Pereira MG, Oliveira L, Mendlowicz MV, Fiszman A, Marques-Portella C, et. al. Decreased premotor cortex volume in victims of urban violence with posttraumatic stress disorder. PLoS One. 2012;7:e42560. obsessive-compulsive disorder,9090. Fontenelle LF, Bramati IE, Moll J, Mendlowicz MV, de Oliveira-Souza R, Tovar-Moll F. White matter changes in OCD revealed by diffusion tensor imaging. CNS Spectr. 2011;16:101-9.

91. Fontenelle LF, Frydman I, Hoefle S, Oliveira-Souza R, Vigne P, Bortolini TS, et. al. Decoding moral emotions in obsessive-compulsive disorder. Neuroimage Clin. 2018;19:82-9.
-9292. Andrade JB, Ferreira FM, Suo C, Yücel M, Frydman I, Monteiro M, et al. An MRI study of the metabolic and structural abnormalities in obsessive-compulsive disorder. Front Hum Neurosci. 2019;13:186. and ADHD,9393. Cocchi L, Bramati IE, Zalesky A, Furukawa E, Fontenelle LF, Moll J, et al. Altered functional brain connectivity in a non-clinical sample of young adults with attention-deficit/hyperactivity disorder. J Neurosci. 2012;32:17753-61. often in collaboration with radiologists and basic neuroscientists from the privately funded D’Or Institute of Research and Education (IDOR). The IDOR group pioneered the use of task-related fMRI in studies performed entirely in Brazil in the early 2000s.9494. Moll J, de Oliveira-Souza R, Passman LJ, Cunha FC, Souza-Lima F, Andreiuolo PA. Functional MRI correlates of real and imagined tool-use pantomimes. Neurology. 2000;54:1331-6.,9595. Moll J, de Oliveira-Souza R, Bramati IE, Grafman J. Functional networks in emotional moral and nonmoral social judgments. Neuroimage. 2002;16:696-703. They have since led a series of sophisticated studies in healthy subjects evaluating aspects of emotional processing and social behavior,9696. Moll J, Bado P, de Oliveira-Souza R, Bramati IE, Lima DO, Paiva FF, et al. A neural signature of affiliative emotion in the human septohypothalamic area. J Neurosci. 2012;32:12499-505.,9797. Zahn R, Moll J, Paiva M, Garrido G, Krueger F, Huey ED, et al. The neural basis of human social values: evidence from functional MRI. Cereb Cortex. 2009;19:276-83. as well as MRI studies on samples of subjects with major depression9898. Workman CI, Lythe KE, McKie S, Moll J, Gethin JA, Deakin JF, et al. Subgenual cingulate-amygdala functional disconnection and vulnerability to melancholic depression. Neuropsychopharmacology. 2016;41:2082-90. and personality disorders.9999. de Oliveira-Souza R, Hare RD, Bramati IE, Garrido GJ, Ignácio FA, Tovar-Moll F, et al. Psychopathy as a disorder of the moral brain: fronto-temporo-limbic grey matter reductions demonstrated by voxel-based morphometry. Neuroimage. 2008;40:1202-13.,100100. Sato JR, de Oliveira-Souza R, Thomaz CE, Basílio R, Bramati IE, Amaro E Jr, et al. Identification of psychopathic individuals using pattern classification of MRI images. Soc Neurosci. 2011;6:627-39. Additionally, in Rio de Janeiro, neuroscientists from the Fluminense Federal University (UFF) have conducted studies investigating neuroimaging features associated with emotional processing in healthy humans101101. Lobo I, David IA, Figueira I, Campagnoli RR, Volchan E, Pereira MG, et al. Brain reactivity to unpleasant stimuli is associated with severity of posttraumatic stress symptoms. Biol Psychol. 2014;103:233-41.

102. Mourão-Miranda J, Volchan E, Moll J, de Oliveira-Souza R, Oliveira L, Bramati I, et al. Contributions of stimulus valence and arousal to visual activation during emotional perception. Neuroimage. 2003;20:1955-63.
-103103. Sanchez TA, Mocaiber I, Erthal FS, Joffily M, Volchan E, Pereira MG, et al. Amygdala responses to unpleasant pictures are influenced by task demands and positive affect trait. Front Hum Neurosci. 2015;9:107. and subjects with psychiatric disorders,104104. Mocaiber I, Sanchez TA, Pereira MG, Erthal FS, Joffily M, Araujo DB, et al. Antecedent descriptions change brain reactivity to emotional stimuli: a functional magnetic resonance imaging study of an extrinsic and incidental reappraisal strategy. Neuroscience. 2011;193:241-8. often in collaboration with colleagues from the IDOR and UFRJ. In regard to other Brazilian states, a group from the Federal University of Bahia (UFBA) undertook MRI studies of bipolar disorder in collaboration with other centers.105105. Miranda-Scippa AM, Pires ML, Handfas BW, Marie SK, Calil HM. Pituitary volume and the effects of phototherapy in patients with seasonal winter depression: a controlled study. Braz J Psychiatry. 2008;30:50-4.

106. Nery-Fernandes F, Rocha MV, Jackowski A, Ladeia G, Guimarães JL, Quarantini LC, et al. Reduced posterior corpus callosum area in suicidal and non-suicidal patients with bipolar disorder. J Affect Disord. 2012;142:150-5.
-107107. Rocha MV, Nery-Fernandes F, Guimarães JL, Quarantini Lde C, de Oliveira IR, Ladeia-Rocha GG, et al. Normal metabolic levels in prefrontal cortex in euthymic bipolar I patients with and without suicide attempts. Neural Plast. 2015;2015:165180. At the Federal University of Rio Grande do Norte (UFRN) Brain Institute, physicists and neuroscientists have pioneered neuroimaging investigations of humans using the psychedelic drug ayahuasca,108108. de Araujo DB, Ribeiro S, Cecchi GA, Carvalho FM, Sanchez TA, Pinto JP, et al. Seeing with the eyes shut: neural basis of enhanced imagery following Ayahuasca ingestion. Hum Brain Mapp. 2012;33:2550-60.,109109. Viol A, Palhano-Fontes F, Onias H, de Araujo DB, Viswanathan GM. Shannon entropy of brain functional complex networks under the influence of the psychedelic Ayahuasca. Sci Rep. 2017;7:7388. and have established collaborations with other groups in Brazil110110. Sanches RF, de Lima Osório F, Dos Santos RG, Macedo LR, Maia-de-Oliveira JP, Wichert-Ana L, et al. Antidepressant effects of a single dose of Ayahuasca in patients with recurrent depression: a SPECT study. J Clin Psychopharmacol. 2016;36:77-81. and abroad.111111. Palaniyappan L, Mota NB, Oowise S, Balain V, Copelli M, Ribeiro S, et al. Speech structure links the neural and socio-behavioural correlates of psychotic disorders. Prog Neuropsychopharmacol Biol Psychiatry. 2019;88:112-20. Psychiatrists from the Federal University of Ceará (UFCE) have also collaborated in original studies of mood disorders with other groups in Brazil3434. Machado-Vieira R, Zanetti MV, Otaduy MC, De Sousa RT, Soeiro-de-Souza MG, Costa AC, et al. Increased brain lactate during depressive episodes and reversal effects by lithium monotherapy in drug-naive bipolar disorder: a 3-T 1H-MRS study. J Clin Psychopharmacol. 2017;37:40-5. and abroad.112112. Knöchel C, Schmied C, Linden DE, Stäblein M, Prvulovic D, de Carvalho LA, et al. White matter abnormalities in the fornix are linked to cognitive performance in SZ but not in BD disorder: an exploratory analysis with DTI deterministic tractography. J Affect Disord. 2016;201:64-78.,113113. Alves GS, Knöchel C, Paulitsch MA, Reinke B, Carvalho AF, Feddern R, et al. White matter microstructural changes and episodic memory disturbances in late-onset bipolar disorder. Front Psychiatry. 2018;9:480. Finally, groups of psychiatrists based at other public universities in different states in Brazil have regularly published well-cited systematic reviews and meta-analyses on several neuroimaging topics.114114. Milani AC, Hoffmann EV, Fossaluza V, Jackowski AP, Mello MF. Does pediatric post-traumatic stress disorder alter the brain? Systematic review and meta-analysis of structural and functional magnetic resonance imaging studies. Psychiatry Clin Neurosci. 2017;71:154-69.

115. Pereira LP, Köhler CA, de Sousa RT, Solmi M, de Freitas BP, Fornaro M, et al. The relationship between genetic risk variants with brain structure and function in bipolar disorder: a systematic review of genetic-neuroimaging studies. Neurosci Biobehav Rev. 2017;79:87-109.

116. Dos Santos RG, Osório FL, Crippa JA, Hallak JE. Classical hallucinogens and neuroimaging: a systematic review of human studies: hallucinogens and neuroimaging. Neurosci Biobehav Rev. 2016;71:715-28.

117. Frydman I, Andrade JB, Vigne P, Fontenelle LF. Can neuroimaging provide reliable biomarkers for Obsessive-Compulsive disorder? A narrative review. Curr Psychiatry Rep. 2016;18:90.

118. Mochcovitch MD, Freire RC, Garcia RF, Nardi AE. A systematic review of fMRI studies in generalized anxiety disorder: evaluating its neural and cognitive basis. J Affect Disord. 2014;167:336-42.

119. Busatto GF. Structural and functional neuroimaging studies in major depressive disorder with psychotic features: a critical review. Schizophr Bull. 2013;39:776-86.

120. Gonzalez MO, Goudriaan AE, Périco CA, Campos MW, de Andrade AG, Bhugra D, et al. Neural correlates of depressive symptoms in smokers – a systematic review of imaging studies. Subst Use Misuse. 2017;52:1809-22.

121. de-Almeida CP, Wenzel A, de-Carvalho CS, Powell VB, Araújo-Neto C, Quarantini LC, et al. CNS Spectr. 2012;17:70-5.

122. Porto PR, Oliveira L, Mari J, Volchan E, Figueira I, Ventura P. Does cognitive behavioral therapy change the brain? A systematic review of neuroimaging in anxiety disorders. J Neuropsychiatry Clin Neurosci. 2009;21:114-25.

123. Magalhaes AA, Oliveira L, Pereira MG, Menezes CB. Does meditation alter brain responses to negative stimuli? A systematic review. Front Hum Neurosci. 2018;12:448.

124. Grangeon MC, Seixas C, Quarantini LC, Miranda-Scippa A, Pompili M, Steffens DC, et al. White matter hyperintensities and their association with suicidality in major affective disorders: a meta-analysis of magnetic resonance imaging studies. CNS Spectr. 2010;15:375-81.
-125125. Beraldi GH, Prado KS, Amann BL, Radua J, Friedman L, Elkis H. Meta-analyses of cavum septum pellucidum in mood disorders in comparison with healthy controls or schizophrenia. Eur Neuropsychopharmacol. 2018;28:1325-38.

There are two additional Brazilian research centers dedicated primarily to neurophysiology and neurology that deserve to be mentioned here. At the privately funded Albert Einstein Israelite Hospital in São Paulo, a group of neuroradiologists and neuroscientists has conducted a series of MRI investigations evaluating interventions of potential interest to psychiatry using yoga-based and other meditation methods.126126. Kozasa EH, Sato JR, Lacerda SS, Barreiros MA, Radvany J, Russell TA, et al. Meditation training increases brain efficiency in an attention task. Neuroimage. 2012;59:745-9.,127127. Rodrigues DB, Lacerda SS, Balardin JB, Chaim KT, Portes B, Sanches-Rocha LG, et al. Posterior cingulate cortex/precuneus blood oxygen-level dependent signal changes during the repetition of an attention task in meditators and nonmeditators. Neuroreport. 2018;29:1463-7. They have also performed fMRI studies on emotional processing128128. Kraft I, Balardin JB, Sato JR, Sommer J, Tobo P, Barrichello C, et al. Quality of life is related to the functional connectivity of the default mode network at rest. Brain Imaging Behav. 2019;13:1418-26.

129. Caous CA, Tobo PR, Talarico VH, Gonçales LR, Yoshimine E, Cruz AC Jr, et al. Modulation of cerebral haemodynamic response to olfactory stimuli by emotional valence detected by functional magnetic resonance imaging. Dement Neuropsychol. 2015;9:405-12.
-130130. Pires FB, Lacerda SS, Balardin JB, Portes B, Tobo PR, Barrichello CR, et al. Self-compassion is associated with less stress and depression and greater attention and brain response to affective stimuli in women managers. BMC Womens Health. 2018;18:195. and liased with psychiatrists from UNIFESP in SPECT investigations.5151. Felicio AC, Moriyama TS, Godeiro-Junior C, Shih MC, Hoexter MQ, Borges V, et al. Higher dopamine transporter density in Parkinson's disease patients with depression. Psychopharmacology (Berl). 2010;211:27-31. Finally, the State University of Campinas (UNICAMP) in São Paulo houses the Brazilian Institute of Neuroscience and Nanotechnology, funded by FAPESP. With noteworthy scientific output in epilepsy, this group has also performed a few investigations on psychiatric disorders including autism131131. Pereira AM, Campos BM, Coan AC, Pegoraro LF, de Rezende TJ, Obeso I, et al. Differences in cortical structure and functional MRI connectivity in high functioning autism. Front Neurol. 2018;9:539. and mood disorders132132. Garcia DS, Polydoro MS, Alvim MK, Ishikawa A, Moreira JC, Nogueira MH, et al. Anxiety and depression symptoms disrupt resting state connectivity in patients with genetic generalized epilepsies. Epilepsia. 2019;60:679-88. in association with local groups of psychiatrists, and conducted several MRI studies on mild cognitive impairment (MCI) and Alzheimer’s disease (AD).133133. Balthazar ML, de Campos BM, Franco AR, Damasceno BP, Cendes F. Whole cortical and default mode network mean functional connectivity as potential biomarkers for mild Alzheimer's disease. Psychiatry Res. 2014;221:37-42.

134. Balthazar ML, Pereira FR, Lopes TM, da Silva EL, Coan AC, Campos BM, et al. Neuropsychiatric symptoms in Alzheimer's disease are related to functional connectivity alterations in the salience network. Hum Brain Mapp. 2014;35:1237-46.
-135135. Teixeira CV, Rezende TJ, Weiler M, Magalhães TN, Carletti-Cassani AF, Silva TQ, et al. Cognitive and structural cerebral changes in amnestic mild cognitive impairment due to Alzheimer's disease after multicomponent training. Alzheimers Dement (N Y). 2018;4:473-80. Studies of healthy aging, MCI, and AD are relevant in this context because they are at the interface between psychiatry and neurology; neuroimaging investigations in this field have been carried out by groups at HCFMUSP,136136. Busatto GF, Garrido GE, Almeida OP, Castro CC, Camargo CH, Cid CG, et al. A voxel-based morphometry study of temporal lobe gray matter reductions in Alzheimer's disease. Neurobiol Aging. 2003;24:221-31.

137. Bottino CM, Castro CC, Gomes RL, Buchpiguel CA, Marchetti RL, Neto MR. Volumetric MRI measurements can differentiate Alzheimer's disease, mild cognitive impairment, and normal aging. Int Psychogeriatr. 2002;14:59-72.
-138138. Porto FH, Coutinho AM, Pinto AL, Gualano B, Duran FL, Prando S, et al. Effects of aerobic training on cognition and brain glucose metabolism in subjects with mild cognitive impairment. J Alzheimers Dis. 2015;46:747-60. FMRP-USP,139139. da Silva Filho SR, Barbosa JH, Rondinoni C, Dos Santos AC, Salmon CE, da Costa Lima NK, et al. Neuro-degeneration profile of Alzheimer's patients: a brain morphometry study. Neuroimage Clin. 2017;15:15-24. and UNIFESP140140. Baldaçara L, Borgio JG, Moraes WA, Lacerda AL, Montaño MB, Tufik S, et al. Cerebellar volume in patients with dementia. Braz J Psychiatry. 2011;33:122-9.,141141. Vasconcelos LG, Jackowski AP, Oliveira MO, Flor YM, Souza AA, Bueno OF, et al. The thickness of posterior cortical areas is related to executive dysfunction in Alzheimer's disease. Clinics (Sao Paulo). 2014;69:28-37. in the state of São Paulo, as well at the UFMG,142142. Resende EP, Rosen HJ, Chiang K, Staffaroni AM, Allen I, Grinberg LT, et al. Primary school education may be sufficient to moderate a memory-hippocampal relationship. Front Aging Neurosci. 2018;10:381. UFRJ,143143. Engelhardt E, Moreira DM, Laks J, Marinho VM, Rozenthal M, Oliveira AC Jr. [Alzheimer's disease and magnetic resonance spectroscopy of the hippocampus]. Arq Neuropsiquiatr. 2001;59:865-70.,144144. Sudo FK, Alves CE, Alves GS, Ericeira-Valente L, Tiel C, Moreira DM, et al. White matter hyperintensities, executive function and global cognitive performance in vascular mild cognitive impairment. Arq Neuropsiquiatr. 2013;71:431-6. and the Federal University of Pernambuco (UFPE).145145. Menezes TL, Andrade-Valença LP, Valença MM. Magnetic resonance imaging study cannot individually distinguish individuals with mild cognitive impairment, mild Alzheimer's disease, and normal aging. Arq Neuropsiquiatr. 2013;71:207-12.

A map of Brazil showing the official names and location of each of the institutions cited above is provided in Figure 1.

Table 2 and the graph provided in Figure 2A show the growth of psychiatric neuroimaging studies in recent decades in Brazil, as expressed by the total number of publications from 2000 onwards (n=478). Of these papers, 61.3% directly addressed psychiatric disorders across the life span, with the remaining publications covering brain aging, AD, and MCI (21.1%), emotional processing and social behavior in healthy humans (6.9%), brain effects of drugs in healthy subjects (4.6%), brain development in children and adolescents (4.4%), and studies of yoga and meditation practices (1.7%). Table 2 also indicates the high proportion of original studies and meta-analyses relative to literature reviews. The methods that were used to identify those publications are outlined in the online-only supplementary material.

Table 2
Characteristics of psychiatric neuroimaging publications from Brazilian research groups from the year 2000 onwards

Most Brazilian research groups mentioned above have regularly collaborated with each other. Additionally, in many of their initiatives, international collaboration has been of critical relevance. As shown in Table 2, to date 50% of psychiatric neuroimaging publications involving Brazilian groups have co-authors from non-Brazilian institutions. Of 478 papers, over 70% were led by researchers based in Brazil (first or senior authors), while the remaining publications were led by scientists from foreign institutions with Brazilian co-authorship. Most international collaborations have been established with researchers from the United Kingdom (UK) and United States, but several other countries are represented, including Germany, Australia, Canada, the Netherlands, Spain, Italy, France, China, Japan, Turkey, Sweden, Denmark, and Switzerland, as well as Argentina and Chile in South America. Additionally, a Brazilian physician with undergraduate and psychiatric training at USP in the 1990s (Jair C. Soares) moved soon thereafter to the United States to become a world leader in psychiatric neuroimaging research. As such, he has opened the doors of his research labs to several Brazilian students over the years.146146. Caetano SC, Olvera RL, Hatch JP, Sanches M, Chen HH, Nicoletti M, et al. Lower N-acetyl-aspartate levels in prefrontal cortices in pediatric bipolar disorder: a 1H magnetic resonance spectroscopy study. J Am Acad Child Adolesc Psychiatry. 2011;50:85-94.

147. Nery FG, Hatch JP, Nicoletti MA, Monkul ES, Najt P, Matsuo K, et al. Temperament and character traits in major depressive disorder: influence of mood state and recurrence of episodes. Depress Anxiety. 2009;26:382-8.
-148148. Zanetti MV, Soloff PH, Nicoletti MA, Hatch JP, Brambilla P, Keshavan MS, et al. MRI study of corpus callosum in patients with borderline personality disorder: a pilot study. Prog Neuropsychopharmacol Biol Psychiatry. 2007;31:1519-25. Finally, other psychiatrists and computer scientists with doctoral or postdoctoral neuroimaging research training in Brazilian universities now hold academic positions in North America and Europe, providing additional opportunities for continued collaboration with scientists in Brazil.149149. Almeida JR, Greenberg T, Lu H, Chase HW, Fournier JC, Cooper CM, et al. Test-retest reliability of cerebral blood flow in healthy individuals using arterial spin labeling: findings from the EMBARC study. Magn Reson Imaging. 2018;45:26-33.

150. Fernandes O Jr, Portugal LC, Alves RC, Arruda-Sanchez T, Rao A, Volchan E, et al. Decoding negative affect personality trait from patterns of brain activation to threat stimuli. Neuroimage. 2017;145:337-45.
-151151. Ferreira LK, Rondina JM, Kubo R, Ono CR, Leite CC, Smid J, et al. Support vector machine-based classification of neuroimages in Alzheimer's disease: direct comparison of FDG-PET, rCBF-SPECT and MRI data acquired from the same individuals. Braz J Psychiatry. 2017;40:181-91.

There is also evidence of a progressive increase in the international impact of psychiatric neuroimaging studies in Brazil. As shown in Figure 2B, the number of neuroimaging papers published in high-impact journals (i.e., impact factor above 6, as calculated by Clarivate Analytics) was higher in the 2010s than in the 2000s. As we discuss in subsequent sections of this article, such an increase is substantially explained by a growing number of local studies using large-sized samples and the recent participation of Brazilian groups in international consortia, in addition to the publication of expert reviews in highly cited periodicals.

The synthesis provided herein indicates that psychiatric neuroimaging research in Brazil has grown steadily over the past few decades, with a sizeable international impact. As a whole, the field has flourished to a relatively greater degree in the state of São Paulo than in other Brazilian states. This is possibly related to the existence of more funding opportunities in São Paulo (via FAPESP) and a relatively greater availability of in vivo imaging equipment for research applications. For instance, in four of the São Paulo-based academic institutions mentioned herein, new 3 Tesla MRI equipment were simultaneously installed in the context of a large-scale program launched by FAPESP in 2004.152152. Cooperação Interinstitucional de Apoio a Pesquisas sobre o Cérebro (CInAPCe) da FAPESP. [Internet]. 2019 [cited 2019 Oct 3]. www.fapesp.br/1896
www.fapesp.br/1896...
Additionally, the persistence of experienced São Paulo-based psychiatrists and other mental health professionals may have served to maintain a high level of motivation and nurture a local sense of empowerment to overcome technological challenges.

Recent neuroimaging advances applicable to psychiatric research

Technical neuroimaging developments are unfolding at the present time at a pace that is quicker than ever. This presses research groups to swiftly incorporate such innovations, providing exciting opportunities for novel investigations. Selected key examples of incremental innovation recently incorporated in MRI and PET research studies in Brazil are described below.

New approaches for the extraction of quantitative neuroimage indices

In conventional neuroimaging study designs, statistical tests are applied on mean group data after extracting quantitative information from individual imaging datasets (for instance, volumetric measures using structural MRI data or local brain uptake of radiotracers in PET or SPECT studies). Quantitative data from images are usually extracted with regions of interest of predefined anatomical borders placed on selected brain portions, or using automated voxel-based methods.

One fascinating aspect of brain research is the fast-paced incorporation of computational techniques capable of extracting novel and varied quantitative indices from neuroimaging datasets using traditional, readily applicable data acquisition protocols. One recent example is given by new, automatic processing methods for surface-based analyses of structural MRI data, which allow for the decomposition of regional brain cortical volumes into its two components, namely, cortical thickness and cortical area. These two cortical surface phenotypes, which are not directly correlated with each other,153153. Winkler AM, Kochunov P, Blangero J, Almasy L, Zilles K, Fox PT, et al. Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies. Neuroimage. 2010;53:1135-46. are formed over separate time frames and through different mechanisms during brain development154154. Budday S, Steinmann P, Kuhl E. Physical biology of human brain development. Front Cell Neurosci. 2015;9:257. and have distinct patterns of genetic heritability.155155. Blokland GA, de Zubicaray GI, McMahon KL, Wright MJ. Genetic and environmental influences on neuroimaging phenotypes: a meta-analytical perspective on twin imaging studies. Twin Res Hum Genet. 2012;15:351-71.,156156. Panizzon MS, Fennema-Notestine C, Eyler LT, Jernigan TL, Prom-Wormley E, Neale M, et al. Distinct genetic influences on cortical surface area and cortical thickness. Cereb Cortex. 2009;19:2728-35. Recent automated MRI processing methods also allow reproducible measurements of the degree of local cortical gyrification (which is directly related to the development of neuronal connectivity at early periods of cortical maturation),157157. Ronan L, Fletcher PC. From genes to folds: a review of cortical gyrification theory. Brain Struct Funct. 2015;220:2475-83. regional brain shape and texture,158158. Gryglewski G, Baldinger-Melich P, Seiger R, Godbersen GM, Michenthaler P, Klöbl M, et al. Structural changes in amygdala nuclei, hippocampal subfields and cortical thickness following electroconvulsive therapy in treatment-resistant depression: longitudinal analysis. Br J Psychiatry. 2019;214:159-67. and subfield volumes of brain structures of key relevance to psychiatry, such as the hippocampus.159159. Iglesias JE, Augustinack JC, Nguyen K, Player CM, Player A, Wright M, et al. Alzheimer's Disease Neuroimaging Initiative. A computational atlas of the hippocampal formation using ex vivo, ultra-high resolution MRI: application to adaptive segmentation of in vivo MRI. Neuroimage. 2015;115:117-37. The separate measurement of these MRI-based indices in neuroimaging studies opens exciting opportunities for the generation of data on the type and timing of structural brain abnormality associated with various psychiatric disorders and for the investigation of the correlations between brain imaging indices and genetic and environmental variables, history of treatment exposure, and other disease-related factors.

An increase in the number of neuroimaging investigations using the above-mentioned automated processing methods is expected, given their progressive availability. However, there is also a highly critical need to apply systematic quality control procedures in such MRI studies to detect occasional errors in cortical delineation and volume measurements that require either correction or the exclusion of participants.160160. Ducharme S, Albaugh MD, Nguyen TV, Hudziak JJ, Mateos-Pérez JM, Labbe A, et al. Brain Development Cooperative Group. Trajectories of cortical thickness maturation in normal brain development--the importance of quality control procedures. Neuroimage. 2016;125:267-79.

Innovative methods of data acquisition

PET and SPECT devices are highly adaptable to incorporate image acquisition protocols to quantify the brain distribution of new radiopharmaceuticals of interest to psychiatry.161161. Benadiba M, Luurtsema G, Wichert-Ana L, Buchpigel CA, Busatto Filho G. New molecular targets for PET and SPECT imaging in neurodegenerative diseases. Braz J Psychiatry. 2012;34 Suppl 2:S125-36. In Brazilian facilities providing an on-site cyclotron together with experienced teams of radiopharmacists and physicists, new PET probes have been incorporated for research purposes in recent years, such as Pittsburgh compound B labeled with carbon-11 (11C-PiB) for the mapping of extracellular amyloid plaques formed by amyloid β-peptide (Aβ) in the cerebral cortex (see Figure 3),162162. Faria DP, Duran FL, Squarzoni P, Coutinho AM, Garcez AT, Santos PP, et al. Topography of 11C-Pittsburgh compound B uptake in Alzheimer's disease: a voxel-based investigation of cortical and white matter regions. Braz J Psychiatry. 2019;41:101-11. and18F-FDG PET for the evaluation of brain metabolism. The LiNC group at UNIFESP has also pioneered studies using 99mTc-TRODAT to evaluate the density of striatal dopaminergic terminals with SPECT.8080. Silva N Jr, Szobot CM, Shih MC, Hoexter MQ, Anselmi CE, Pechansky F, et al. Searching for a neurobiological basis for self-medication theory in ADHD comorbid with substance use disorders: an in vivo study of dopamine transporters using (99m)Tc-TRODAT-1 SPECT. Clin Nucl Med. 2014;39:e129-34.

Figure 3
Positron emission tomography (PET) images acquired after intravenous injection of Pittsburgh compound B labeled with carbon-11 (11C-PiB) to map the anomalous deposition of extracellular amyloid plaques formed by amyloid β-peptide (Aβ) in the cerebral cortex. Top panel: transaxial slices from a usual 11C-PiB PET dataset obtained from a healthy elderly volunteer, with very low tracer uptake in the cortex relative to white matter uptake. Bottom panel: 11C-PiB PET data from a patient suffering from dementia compatible with Alzheimer’s disease (AD), with increased tracer uptake in the frontal, temporal, parietal, and cingulate cortices. Both datasets underwent automated processing typically employed in quantitative neuroimaging research studies, including spatial normalization to a standardized anatomical template (using the Statistical Parametric Mapping program) and correction for partial volume effects based on information from volumetric magnetic resonance imaging (MRI) datasets obtained from the same individuals. The original, preprocessed PET images were obtained in collaboration with scientists from the Centro de Medicina Nuclear, Instituto de Radiologia, Hospital de Clínicas, Faculdade de Medicina, Universidade de São Paulo, under the leadership of Dr. Daniele de Paula Faria and Prof. Carlos A. Buchpiguel.

Concerning MRI, several new image acquisition methods of interest to psychiatry have been incorporated in studies led by Brazilian research groups in the past few years, including diffusion tensor imaging (DTI) for investigations of the microstructural integrity of white matter fibers and tracts, with acquisition of diffusion-weighted imaging (DWI) data (which measures the motion of water molecules within minute tissue portions),163163. Chaim-Avancini TM, Doshi J, Zanetti MV, Erus G, Silva MA, Duran FL, et al. Neurobiological support to the diagnosis of ADHD in stimulant-naïve adults: pattern recognition analyses of MRI data. Acta Psychiatr Scand. 2017;136:623-36. and resting-state fMRI methods for the investigation of intra- and internetwork patterns of functional connectivity in the brain at rest.164164. Ferreira LK, Regina AC, Kovacevic N, Martin Mda G, Santos PP, Carneiro Cde G, et al. Aging effects on whole-brain functional connectivity in adults free of cognitive and psychiatric disorders. Cereb Cortex. 2016;26:3851-65. There is continuous innovation in MRI acquisition methods. A very recent example is the acquisition of DWI data using a “multishell” imaging approach, which relies on a high angular resolution diffusion imaging (HARDI) protocol165165. Tuch DS, Reese TG, Wiegell MR, Makris N, Belliveau JW, Wedeen VJ. High angular resolution diffusion imaging reveals intravoxel white matter fiber heterogeneity. Magn Reson Med. 2002;48:577-82. combined with data acquisition with more than one electromagnetic field strength.166166. Cheng J, Shen D, Yap PT, Basser PJ. Novel single and multiple shell uniform sampling schemes for diffusion MRI using spherical codes. Med Image Comput Comput Assist Interv. 2015;9349:28-36. This allows the use of new mathematical models to generate quantitative indices of gray matter microstructure at the level of axonal and dendritic projections (neurites) in techniques such as neurite orientation dispersion and density imaging (NODDI)167167. Zhang H, Schneider T, Wheeler-Kingshott CA, Alexander DC. NODDI: practical in vivo neurite orientation dispersion and density imaging of the human brain. Neuroimage. 2012;61:1000-16. (Figure 4). MRI studies using NODDI now provide unique opportunities for the in vivo mapping of dendrite pathological changes and other neurite abnormalities that were only previously accessible using post-mortem histological techniques.168168. Nazeri A, Mulsant BH, Rajji TK, Levesque ML, Pipitone J, Stefanik L, et al. Gray matter neuritic microstructure deficits in schizophrenia and bipolar disorder. Biol Psychiatry. 2017;82:726-36.

Figure 4
A) Illustrative depiction of neurite density and orientation dispersion (arborization) of dendritic trees within the cerebral cortex. Brain cortical variations in such microstructural gray matter indices, which may be present in patients with psychiatric disorders, can now be assessed using neurite orientation dispersion and density imaging (NODDI).167167. Zhang H, Schneider T, Wheeler-Kingshott CA, Alexander DC. NODDI: practical in vivo neurite orientation dispersion and density imaging of the human brain. Neuroimage. 2012;61:1000-16. NODDI requires multishell/high angular resolution diffusion imaging (HARDI) acquisitions using magnetic resonance imaging (MRI). Please note that the figure is only meant for illustration and does not represent the actual spatial resolution achieved by NODDI (adapted from Genç et al.,169169. Genç E, Fraenz C, Schlüter C, Friedrich P, Hossiep R, Voelkle MC, et al. Diffusion markers of dendritic density and arborization in gray matter predict differences in intelligence. Nat Commun. 2018;9:1905. licensed under Creative Commons Attribution 4.0 International License). B) 3D schematic representation of a multishell encoding scheme generated using a gradient tool available at the Multiple Acquisitions for Standardization of Structural Imaging Validation and Evaluation (MASSIVE) website (http://www.massive-data.org/). The gradients (colored dots) are magnetic field pulses that sensitize diffusion in a particular direction; by doing this, MRI scans can obtain information related to the dispersion of water molecules for each voxel. The colored dots show each randomly defined gradient direction. For each shell, there is an operator-selected parameter called the b-factor that defines gradient strength and duration. In this example, each gray circumference represents one of the shells: the inner one has a b-value of 1,000 s/mm2 (gradients represented in pink); the outermost one has a b-value of 3,000 s/mm2 (dark blue gradients); and, in between, a shell with a b-value of 2,000 s/mm2 (green gradients). The grey dots represent the diametrically opposite end of each gradient, i.e., the line (not shown) linking a colored dot to a grey dot is the gradient axis. This representation exemplifies how MRI acquisition protocols can be designed to measure the dispersion and orientation of water molecules to generate quantitative indices of gray matter microstructure at the level of neurites with NODDI.167167. Zhang H, Schneider T, Wheeler-Kingshott CA, Alexander DC. NODDI: practical in vivo neurite orientation dispersion and density imaging of the human brain. Neuroimage. 2012;61:1000-16.

Finally, the applicability of other in vivo imaging methods is also growing, most notably functional near infrared spectroscopy (fNIRS). This method, which provides measures of cortical brain activity with superior temporal resolution, high portability and low cost, has been recently used by Brazilian groups in studies of affective processing170170. Trambaiolli LR, Biazoli CE Jr, Cravo AM, Falk TH, Sato JR. Functional near-infrared spectroscopy-based affective neurofeedback: feedback effect, illiteracy phenomena, and whole-connectivity profiles. Neurophotonics. 2018;5:035009. and other areas of potential interest to psychiatry.171171. Bandeira JS, Antunes LC, Soldatelli MD, Sato JR, Fregni F, Caumo W. Functional spectroscopy mapping of pain processing cortical areas during non-painful peripheral electrical stimulation of the accessory spinal nerve. Front Hum Neurosci. 2019;13:200. The fNIRS technique will probably become an important neuroimaging resource in environments with limited research funding opportunities. Additionally, it offers exciting opportunities by making use of reliable wireless devices that are suitable for implementing brain-computer interfaces and bedside investigations.

The need for large samples

In recent years, significant concerns have been raised regarding the validity and reproducibility of biomedical research.172172. Ioannidis JP. Why most published research findings are false. PLoS Med. 2005;2:e124. Particularly, it has been stressed that studies commonly have small sample sizes and consequently low statistical power, thus reducing the chance of detecting a true effect and reducing the probability that a statistically significant result has an accurate effect size.173173. Button KS, Ioannidis JP, Mokrysz C, Nosek BA, Flint J, Robinson ES, et al. Power failure: why small sample size undermines the reliability of neuroscience. Nat Rev Neurosci. 2013;14:365-76. Review. Erratum 2013;14:451. Furthermore, replication studies are seldom performed and frequently have sample sizes similar to those of the original investigation, again jeopardizing the ability to determine whether a given finding is actually true or not. There is a frequent association between small-sized samples and inferior quality of study design, selective data analysis, inability to properly treat nuisance factors, and imprecise reporting of outcomes, with all these factors further undermining the validity and reproducibility of results.173173. Button KS, Ioannidis JP, Mokrysz C, Nosek BA, Flint J, Robinson ES, et al. Power failure: why small sample size undermines the reliability of neuroscience. Nat Rev Neurosci. 2013;14:365-76. Review. Erratum 2013;14:451. Such fierce criticism has led to questions regarding the ethics of conducting studies with small samples,173173. Button KS, Ioannidis JP, Mokrysz C, Nosek BA, Flint J, Robinson ES, et al. Power failure: why small sample size undermines the reliability of neuroscience. Nat Rev Neurosci. 2013;14:365-76. Review. Erratum 2013;14:451. since unreliable research may waste scarce resources and mostly produce false findings.172172. Ioannidis JP. Why most published research findings are false. PLoS Med. 2005;2:e124. Fortunately, recent guidelines have been published with the aim of maximizing the validity and reproducibility of the results of biomedical studies, which will hopefully lead to better-quality research.173173. Button KS, Ioannidis JP, Mokrysz C, Nosek BA, Flint J, Robinson ES, et al. Power failure: why small sample size undermines the reliability of neuroscience. Nat Rev Neurosci. 2013;14:365-76. Review. Erratum 2013;14:451.

174. Ioannidis JP, Fanelli D, Dunne DD, Goodman SN. Meta-research: evaluation and improvement of research methods and practices. PLoS Biol. 2015;13:e1002264.
-175175. Müller VI, Cieslik EC, Laird AR, Fox PT, Radua J, Mataix-Cols D, et al. Ten simple rules for neuroimaging meta-analysis. Neurosci Biobehav Rev. 2018;84:151-61.

These considerations are also relevant to brain imaging research. It is currently clear whenever possible, psychiatric neuroimaging investigations should include large samples. In Brazil, the first initiative related to this issue consisted of a collaboration between neuroimaging researchers and epidemiologists from the USP and the UK in Europe, who conducted a population-based structural MRI investigation of first-episode psychosis (FEP) patients recruited by active surveillance of mental health services located in the city of São Paulo.176176. Schaufelberger MS, Duran FL, Lappin JM, Scazufca M, Amaro E Jr, Leite CC, et al. Grey matter abnormalities in Brazilians with first-episode psychosis. Br J Psychiatry Suppl. 2007;51:s117-22.,177177. Zanetti MV, Schaufelberger MS, Doshi J, Ou Y, Ferreira LK, Menezes PR, et al. Neuroanatomical pattern classification in a population-based sample of first-episode schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry. 2013;43:116-25. In addition to allowing the identification of over 100 FEP patients with little exposure to psychopharmacological treatment in a relatively short period of time, the epidemiological design of that study provided an opportunity for recruitment of next-door neighbors who were included in a healthy control group strictly matched for socioeconomic status with the FEP sample.176176. Schaufelberger MS, Duran FL, Lappin JM, Scazufca M, Amaro E Jr, Leite CC, et al. Grey matter abnormalities in Brazilians with first-episode psychosis. Br J Psychiatry Suppl. 2007;51:s117-22. The strategy of recruiting large subject samples for neuroimaging studies has since become frequent in Brazil. In addition, MRI databanks are now available, acquired from large cohorts of schizophrenia patients,4444. Zugman A, Pedrini M, Gadelha A, Kempton MJ, Noto CS, Mansur RB, et al. Serum brain-derived neurotrophic factor and cortical thickness are differently related in patients with schizophrenia and controls. Psychiatry Res. 2015;234:84-9.,178178. Leme IB, Gadelha A, Sato JR, Ota VK, Mari JJ, Melaragno MI, et al. Is there an association between cortical thickness, age of onset, and duration of illness in schizophrenia? CNS Spectr. 2013;18:315-21. children and adolescents,5252. Moura LM, Crossley NA, Zugman A, Pan PM, Gadelha A, Del Aquilla MA, et al. Coordinated brain development: exploring the synchrony between changes in grey and white matter during childhood maturation. Brain Imaging Behav. 2017;11:808-17. and elderly subjects from circumscribed urban areas.179179. Alves TC, Scazufca M, Squarzoni P, Duran FL, Tamashiro-Duran JH, Vallada HP, et al. Subtle gray matter changes in temporo-parietal cortex associated with cardiovascular risk factors. J Alzheimers Dis. 2011;27:575-89.

In addition to large-sized, single-site neuroimaging studies, the strategy of conducting mega-analyses of multisite neuroimaging data has also been explored in Brazil. Such initiatives combine data from multiple studies using uniform image preprocessing and analysis procedures. In the first effort of this kind in Brazil, our research group performed a voxel-based morphometry investigation of gray matter volume deficits in a sample of 161 schizophrenia patients and 151 healthy controls combining structural MRI data from four previous studies carried out at USP.180180. Torres US, Duran FL, Schaufelberger MS, Crippa JA, Louzã MR, Sallet PC, et al. Patterns of regional gray matter loss at different stages of schizophrenia: a multisite, cross-sectional VBM study in first-episode and chronic illness. Neuroimage Clin. 2016;12:1-15. With the greater power afforded by combining data from several studies, we showed that FEP patients display only subtle volumetric deficits relative to controls in a circumscribed fronto-temporal-striatal network, while chronic schizophrenia patients present a much more extensive pattern of regional gray matter volume decrement relative to controls.180180. Torres US, Duran FL, Schaufelberger MS, Crippa JA, Louzã MR, Sallet PC, et al. Patterns of regional gray matter loss at different stages of schizophrenia: a multisite, cross-sectional VBM study in first-episode and chronic illness. Neuroimage Clin. 2016;12:1-15.

The combination of samples from several different Brazilian neuroimaging studies has also paved the way for exciting opportunities to take part in international consortia in recent years. The most notable of these international consortia is Enhancing Neuro Imaging Genetics Through Meta-Analysis (ENIGMA) (http://enigma.ini.usc.edu), which brings together an international research network intended to produce meta- and mega-analyses of neuroimaging and genetic data evaluating dozens of psychiatric disorders and other medical conditions.181181. Thompson PM, Stein JL, Medland SE, Hibar DP, Vasquez AA, Renteria ME, et al. The ENIGMA consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging Behav. 2014;8:153-82. Such a large-scale initiative inevitably leads to the inclusion of subjects with a much higher degree of clinical and demographic heterogeneity than single-site or local multiple-site collaborations. Prospective meta-analyses are carried out by ENIGMA teams in which cohorts, hypotheses, and analyses are selected based on certain criteria before any actual result is known.182182. Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, Welch VA, eds. Cochrane Handbook for Systematic Reviews of Interventions version 6.0 (updated July 2019) [Internet]. 2019 [cited 2019 Oct 03]. http://training.cochrane.org/handbook
http://training.cochrane.org/handbook...
This flexibility in data analysis is suitable to address data heterogeneity and thus offers advantages over traditional meta-analyses based on previously published results. A series of recent ENIGMA papers including thousands of subjects have shed light on features of brain abnormalities associated with psychiatric disorders – including for instance widespread reductions in cortical thickness and area among (mostly chronic) schizophrenia subjects relative to controls,183183. van Erp TG, Walton E, Hibar DP, Schmaal L, Jiang W, Glahn DC, et al. Cortical brain abnormalities in 4474 individuals with schizophrenia and 5098 control subjects via the enhancing neuro imaging genetics through meta analysis (ENIGMA) consortium. Biol Psychiatry. 2018;84:644-54. thinner cortices in frontal, temporal, and parietal regions with no associated abnormalities in cortical areas of bipolar disorder patients relative to controls,184184. Hibar DP, Westlye LT, Doan NT, Jahanshad N, Cheung JW, Ching CR, et al. Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group. Mol Psychiatry. 2018;23:932-42. and cortical thickness changes in direct proportion to the use of psychopharmacological agents such as antipsychotics.183183. van Erp TG, Walton E, Hibar DP, Schmaal L, Jiang W, Glahn DC, et al. Cortical brain abnormalities in 4474 individuals with schizophrenia and 5098 control subjects via the enhancing neuro imaging genetics through meta analysis (ENIGMA) consortium. Biol Psychiatry. 2018;84:644-54. Brazilian research groups have recently taken part in ENIGMA studies on schizophrenia,183183. van Erp TG, Walton E, Hibar DP, Schmaal L, Jiang W, Glahn DC, et al. Cortical brain abnormalities in 4474 individuals with schizophrenia and 5098 control subjects via the enhancing neuro imaging genetics through meta analysis (ENIGMA) consortium. Biol Psychiatry. 2018;84:644-54. bipolar disorder,184184. Hibar DP, Westlye LT, Doan NT, Jahanshad N, Cheung JW, Ching CR, et al. Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group. Mol Psychiatry. 2018;23:932-42.,185185. Favre P, Pauling M, Stout J, Hozer F, Sarrazin S, Abé C, et al. Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals. Neuropsychopharmacology. 2019;44:2285-93. major depression,186186. de Kovel CG, Aftanas L, Aleman A, Alexander-Bloch AF, Baune BT, Brack I, et al. No alterations of brain structural asymmetry in major depressive disorder: an ENIGMA consortium analysis. Am J Psychiatry. 2019;176:1039-49. ADHD,187187. Hoogman M, Muetzel R, Guimaraes JP, Shumskaya E, Mennes M, Zwiers MP, et al. Brain imaging of the cortex in ADHD: a coordinated analysis of large-scale clinical and population-based samples. Am J Psychiatry. 2019;176:531-42. obsessive-compulsive disorder,188188. Boedhoe PS, Schmaal L, Abe Y, Ameis SH, Arnold PD, Batistuzzo MC, et al. Distinct subcortical volume alterations in pediatric and adult OCD: a worldwide meta- and mega-analysis. Am J Psychiatry. 2017;174:60-9. autism,189189. van Rooij D, Anagnostou E, Arango C, Auzias G, Behrmann M, Busatto GF, et al. Cortical and subcortical brain morphometry differences between patients with autism spectrum disorder and healthy individuals across the lifespan: results from the ENIGMA ASD working group. Am J Psychiatry. 2018;175:359-69. and brain structural variations in normal individuals.190190. Kong XZ, Mathias SR, Guadalupe T, ENIGMA Laterality Working Group, Glahn DC, Franke B, et al. Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA consortium. Proc Natl Acad Sci U S A. 2018;115:E5154-63.

One final aspect related to the need for large samples in neuroimaging investigations regards the complex management of databases (not only for images but also for demographic data, clinical details, and neuropsychological characteristics of study subjects). It has become mandatory for neuroimaging research groups to incorporate the use of secure, open-source applications, such as Research Electronic Data Capture (REDCAP),191191. Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap) – a metadata-driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. 2009;42:377-81. to capture and manage clinical data, and XNAT to store and organize imaging data.192192. Rotenberg DJ, Chang Q, Potapova N, Wang A, Hon M, Sanches M, et al. The CAMH neuroinformatics platform: a hospital-focused Brain-CODE implementation. Front Neuroinform. 2018;12:77. Such aspects of data management are also critical to allow the necessary integration of imaging datasets with information on peripheral biomarkers acquired from the same subject samples. The adequate integration of neuroimaging and peripheral biomarker datasets is essential to support the testing of hypotheses evaluating the relationship between neuroanatomical and molecular abnormalities in mental disorders.

New statistical approaches

After the development of voxel-based image analysis methods, neuroimaging researchers have struggled with the statistical problems associated with multiple comparisons, given that the unbiased, whole-brain voxel approach involves up to thousands of statistical comparisons conducted on the same imaging databank, even when one single hypothesis is being tested. This problem has become more complex as a result of improvements in imaging equipment that allow acquisition of data with greater spatial resolution and voxels of reduced size (but increased number), increased use of multimodal neuroimaging protocols (as discussed below), and planning of multiple hypotheses to be tested using the same databanks. Although the problem of multiple statistical testing may be minimized with data smoothing, specialized computer science groups have demonstrated that both traditional brain analysis methods (i.e., voxel-based morphometry)193193. Davatzikos C. Why voxel-based morphometric analysis should be used with great caution when characterizing group differences. Neuroimage. 2004;23:17-20.,194194. Ioannidis JP. Excess significance bias in the literature on brain volume abnormalities. Arch Gen Psychiatry. 2011;68:773-80. and techniques developed more recently (surface-based analyses) may still yield results with unacceptably high levels of false-positive results,195195. Greve DN, Fischl B. False positive rates in surface-based anatomical analysis. Neuroimage. 2018;171:6-14. particularly with the use of small smoothing filters on phenotypes, such as cortical area and volume. This problem might be tackled with the use of more stringent statistical thresholds, but this conversely leads to higher and unacceptable false-negative rates (i.e., reduction in statistical power).

More recently, a promising strategy to overcome the multiple testing dilemma involves the use of nonparametric, permutation analysis methods.195195. Greve DN, Fischl B. False positive rates in surface-based anatomical analysis. Neuroimage. 2018;171:6-14. These approaches, which demand few assumptions about the data,196196. Winkler AM, Ridgway GR, Webster MA, Smith SM, Nichols TE. Permutation inference for the general linear model. Neuroimage. 2014;92:381-97. involve in simple terms computer-based randomization of the actual study data over several times and subsequent testing of the probability that a true difference between groups or conditions is statistically greater than the randomized data distribution. This simple but elegant statistical approach accommodates study designs that include nuisance factors and offers an optimal control of false positives196196. Winkler AM, Ridgway GR, Webster MA, Smith SM, Nichols TE. Permutation inference for the general linear model. Neuroimage. 2014;92:381-97. without reducing study power, as it allows for the use of regular statistical thresholds with any smoothing filter.195195. Greve DN, Fischl B. False positive rates in surface-based anatomical analysis. Neuroimage. 2018;171:6-14. Future studies will demonstrate whether earlier research findings in the psychiatric neuroimaging field obtained using conventional statistical testing methods with suboptimal control for false positives will be confirmed by strategies that are better suited to cope with multiple testing problems, such as permutation statistics.

Also aiming to overcome drawbacks of univariate and multiple statistical testing as well as to bring neuroscience findings to the level of individual subjects, other researchers in the field of neuroimaging have employed multivariate statistical models using artificial intelligence (AI) in the last decade.197197. Klöppel S, Abdulkadir A, Jack CR Jr, Koutsouleris N, Mourão-Miranda J, Vemuri P. Diagnostic neuroimaging across diseases. Neuroimage. 2012;61:457-63. AI could be roughly defined as the attempt to emulate natural human intelligence in computer systems, i.e., inserting higher-order cognitive functions (such as learning, reasoning, and self-correction) into machines. Such methods are of interest to psychiatry given their potential to inform individual diagnostic classification, as well as to predict clinical outcomes and responses to therapeutic interventions. In other words, in addition to being a robust means to help reveal neurobiological aspects of psychiatric disorders, AI methods might in the future be used in the development of clinical tools to aid mental health professionals in decision-making (e.g., improving diagnostic accuracy or choosing the right medication) based on reliable biological information.197197. Klöppel S, Abdulkadir A, Jack CR Jr, Koutsouleris N, Mourão-Miranda J, Vemuri P. Diagnostic neuroimaging across diseases. Neuroimage. 2012;61:457-63.,198198. Schrouff J, Rosa MJ, Rondina JM, Marquand AF, Chu C, Ashburner J, et al. PRoNTo: pattern recognition for neuroimaging toolbox. Neuroinformatics. 2013;11:319-37.

One of the branches of AI, machine learning (ML), has been intensely used in recent neuroimaging studies. ML consists of creating mathematical models sensitive to patterns in natural data that can be generalized. In other words, the main goal/focus of ML is to find patterns in data by training a computational model so that it can accurately predict outcomes when subsequently inputted with previously unseen data. Given a specific dataset, two main steps are involved in model generation: first, parameters are defined by training the model with part of the data; then, the model is tested against another sample from the original dataset.197197. Klöppel S, Abdulkadir A, Jack CR Jr, Koutsouleris N, Mourão-Miranda J, Vemuri P. Diagnostic neuroimaging across diseases. Neuroimage. 2012;61:457-63. The most common ML methodology used in neuroimaging studies is support vector machine (SVM), which consists of a discriminative classifier defined by a hyperplane (multidimensional plane) that can differentiate groups; such a hyperplane is the output of an algorithm that has been presented to a training dataset.199199. Thomaz CE, Duran FL, Busatto GF, Gillies DF, Rueckert D. Multivariate statistical differences of MRI samples of the human brain. J Math Imaging Vis. 2007;29:95-106. In neuroimaging investigations, SVM is used as a classification tool to assign an individual to a specific category (for instance, to differentiate patients with a given psychiatric diagnosis from healthy controls or between patients with good vs. poor prognosis over time). The hyperplane is defined using information from one or multiple imaging modalities to generate a signature that differentiates groups with the greatest possible accuracy.198198. Schrouff J, Rosa MJ, Rondina JM, Marquand AF, Chu C, Ashburner J, et al. PRoNTo: pattern recognition for neuroimaging toolbox. Neuroinformatics. 2013;11:319-37.,200200. Serpa MH, Ou Y, Schaufelberger MS, Doshi J, Ferreira LK, Machado-Vieira R, et al. Neuroanatomical classification in a population-based sample of psychotic major depression and bipolar I disorder with 1 year of diagnostic stability. Biomed Res Int. 2014;2014:706157. Psychiatric neuroimaging groups in Brazil have been involved in ML studies of brain aging and dementia,151151. Ferreira LK, Rondina JM, Kubo R, Ono CR, Leite CC, Smid J, et al. Support vector machine-based classification of neuroimages in Alzheimer's disease: direct comparison of FDG-PET, rCBF-SPECT and MRI data acquired from the same individuals. Braz J Psychiatry. 2017;40:181-91.,199199. Thomaz CE, Duran FL, Busatto GF, Gillies DF, Rueckert D. Multivariate statistical differences of MRI samples of the human brain. J Math Imaging Vis. 2007;29:95-106.,201201. de Oliveira AA, Carthery-Goulart MT, Oliveira Júnior PP, Carrettiero DC, Sato JR. Defining multivariate normative rules for healthy aging using neuroimaging and machine learning: an application to Alzheimer's disease. J Alzheimers Dis. 2015;43:201-12. mood disorders,200200. Serpa MH, Ou Y, Schaufelberger MS, Doshi J, Ferreira LK, Machado-Vieira R, et al. Neuroanatomical classification in a population-based sample of psychotic major depression and bipolar I disorder with 1 year of diagnostic stability. Biomed Res Int. 2014;2014:706157. ADHD,163163. Chaim-Avancini TM, Doshi J, Zanetti MV, Erus G, Silva MA, Duran FL, et al. Neurobiological support to the diagnosis of ADHD in stimulant-naïve adults: pattern recognition analyses of MRI data. Acta Psychiatr Scand. 2017;136:623-36. personality disorders,202202. Sato JR, de Araujo Filho GM, de Araujo TB, Bressan RA, de Oliveira PP, Jackowski AP. Can neuroimaging be used as a support to diagnosis of borderline personality disorder? An approach based on computational neuroanatomy and machine learning. J Psychiatr Res. 2012;46:1126-32. obsessive-compulsive disorder,203203. Hoexter MQ, Miguel EC, Diniz JB, Shavitt RG, Busatto GF, Sato JR. Predicting obsessive-compulsive disorder severity combining neuroimaging and machine learning methods. J Affect Disord. 2013;150:1213-6. autism,7474. Sato JR, Hoexter MQ, Oliveira PP Jr, Brammer MJ, MRC AIMS Consortium, Murphy D, et al. Inter-regional cortical thickness correlations are associated with autistic symptoms: a machine-learning approach. J Psychiatr Res. 2013;47:453-9. and schizophrenia-spectrum disorders.177177. Zanetti MV, Schaufelberger MS, Doshi J, Ou Y, Ferreira LK, Menezes PR, et al. Neuroanatomical pattern classification in a population-based sample of first-episode schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry. 2013;43:116-25.,204204. de Moura AM, Pinaya WH, Gadelha A, Zugman A, Noto C, Cordeiro Q, et al. Investigating brain structural patterns in first episode psychosis and schizophrenia using MRI and a machine learning approach. Psychiatry Res Neuroimaging. 2018;275:14-20. In general, the neuroimaging signatures identified in ML studies evaluating psychiatric disorders have not produced clinically meaningful indices of diagnostic accuracy.163163. Chaim-Avancini TM, Doshi J, Zanetti MV, Erus G, Silva MA, Duran FL, et al. Neurobiological support to the diagnosis of ADHD in stimulant-naïve adults: pattern recognition analyses of MRI data. Acta Psychiatr Scand. 2017;136:623-36.,177177. Zanetti MV, Schaufelberger MS, Doshi J, Ou Y, Ferreira LK, Menezes PR, et al. Neuroanatomical pattern classification in a population-based sample of first-episode schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry. 2013;43:116-25.,200200. Serpa MH, Ou Y, Schaufelberger MS, Doshi J, Ferreira LK, Machado-Vieira R, et al. Neuroanatomical classification in a population-based sample of psychotic major depression and bipolar I disorder with 1 year of diagnostic stability. Biomed Res Int. 2014;2014:706157. However, some studies do indicate that objective, ML-based information may in the future be used to influence treatment decisions in some mental disorders if current findings are replicated and extended in future studies with large, population-based samples evaluated prospectively.163163. Chaim-Avancini TM, Doshi J, Zanetti MV, Erus G, Silva MA, Duran FL, et al. Neurobiological support to the diagnosis of ADHD in stimulant-naïve adults: pattern recognition analyses of MRI data. Acta Psychiatr Scand. 2017;136:623-36. If used in large patient samples, ML-based analyses also allow the definition of neurobiological signatures that rely on imaging indices in combination with other sources of information, such as peripheral biomarker data and neurocognitive test scores.

Imaging multimodality as the rule

With the wealth of available imaging protocols and the relatively short times taken to acquire each type of MRI- or PET-based information, multimodality is becoming the rule in psychiatric neuroimaging investigations.205205. Johnston JA, Wang F, Liu J, Blond BN, Wallace A, Liu J, et al. Multimodal neuroimaging of frontolimbic structure and function associated with suicide attempts in adolescents and young adults with bipolar disorder. Am J Psychiatry. 2017;174:667-75. By combining different MRI and PET modalities, neuroimaging research groups now have the opportunity to document interrelationships (or independence) between different types of brain structural, functional, and molecular abnormalities in the same samples of subjects with psychiatric disorders and produce a hierarchical view of the features that most significantly discriminate subjects with a given psychiatric condition from unaffected controls.

For instance, in a study led by our psychiatric neuroimaging group in which we acquired both morphometric MRI and DTI data from the same sample of adult ADHD subjects and healthy controls, the application of the same image processing and statistical inference methods to the two modalities revealed abnormalities in ADHD patients compared with controls mainly affecting white matter microstructure, involving fronto-parieto-temporal circuits.206206. Chaim TM, Zhang T, Zanetti MV, da Silva MA, Louzã MR, Doshi J, et al. Multimodal magnetic resonance imaging study of treatment-naïve adults with attention-deficit/hyperactivity disorder. PLoS One. 2014;9:e110199. More recently, using an expanded sample evaluated with ML-based analysis methods, we confirmed that DTI indices were the features that contributed most prominently to the neuroanatomical signature that best discriminated ADHD patients from controls.163163. Chaim-Avancini TM, Doshi J, Zanetti MV, Erus G, Silva MA, Duran FL, et al. Neurobiological support to the diagnosis of ADHD in stimulant-naïve adults: pattern recognition analyses of MRI data. Acta Psychiatr Scand. 2017;136:623-36.

Challenges and opportunities in our low- to middle-income environment

As illustrated along this article, experienced research groups in Brazil must strive to keep up with the hectic pace of technological innovation in the field of neuroimaging. This is crucial to allow our psychiatric neuroimaging research labs to remain in a favorable position to contribute original investigations of potential impact.

Investment in highly innovative equipment for use in research (rather than clinically) is a complex endeavor which has been restricted almost entirely to a few centers in the Southeast and South of Brazil. At HCFMUSP in São Paulo, for instance, there has been recent investment in infrastructure and research staff to put to work an MRI system of ultrahigh magnetic field strength (7 Tesla) awarded by FAPESP as well as two PET systems for preclinical molecular imaging studies, awarded by the federal government-funded Financiadora de Estudos e Projetos (FINEP) and FAPESP.

However, it is reassuring to confirm that MRI and PET systems used predominantly for clinical purposes may be suitable for a number of state-of-the-art research applications in humans, with few adjustments. In recent years, such arrangements have been useful for imaging studies carried out in different Brazilian centers, where psychiatric neuroimaging groups have liaised with radiologists and nuclear medicine physicians who are open to allocating equipment time for research despite intense clinical demand. However, it will be challenging to keep up with the need to upgrade equipment for such research applications. For instance, the use of 3 Tesla MRI equipment is now almost the rule in brain imaging research. Even though brain MRI datasets acquired with 1.5 Tesla continue to be included in mega- and meta-analyses carried out by large consortia,183183. van Erp TG, Walton E, Hibar DP, Schmaal L, Jiang W, Glahn DC, et al. Cortical brain abnormalities in 4474 individuals with schizophrenia and 5098 control subjects via the enhancing neuro imaging genetics through meta analysis (ENIGMA) consortium. Biol Psychiatry. 2018;84:644-54.

184. Hibar DP, Westlye LT, Doan NT, Jahanshad N, Cheung JW, Ching CR, et al. Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group. Mol Psychiatry. 2018;23:932-42.

185. Favre P, Pauling M, Stout J, Hozer F, Sarrazin S, Abé C, et al. Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals. Neuropsychopharmacology. 2019;44:2285-93.

186. de Kovel CG, Aftanas L, Aleman A, Alexander-Bloch AF, Baune BT, Brack I, et al. No alterations of brain structural asymmetry in major depressive disorder: an ENIGMA consortium analysis. Am J Psychiatry. 2019;176:1039-49.

187. Hoogman M, Muetzel R, Guimaraes JP, Shumskaya E, Mennes M, Zwiers MP, et al. Brain imaging of the cortex in ADHD: a coordinated analysis of large-scale clinical and population-based samples. Am J Psychiatry. 2019;176:531-42.

188. Boedhoe PS, Schmaal L, Abe Y, Ameis SH, Arnold PD, Batistuzzo MC, et al. Distinct subcortical volume alterations in pediatric and adult OCD: a worldwide meta- and mega-analysis. Am J Psychiatry. 2017;174:60-9.

189. van Rooij D, Anagnostou E, Arango C, Auzias G, Behrmann M, Busatto GF, et al. Cortical and subcortical brain morphometry differences between patients with autism spectrum disorder and healthy individuals across the lifespan: results from the ENIGMA ASD working group. Am J Psychiatry. 2018;175:359-69.
-190190. Kong XZ, Mathias SR, Guadalupe T, ENIGMA Laterality Working Group, Glahn DC, Franke B, et al. Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA consortium. Proc Natl Acad Sci U S A. 2018;115:E5154-63. it is progressively more difficult to publish single-site psychiatric neuroimaging studies in highly visible scientific journals with data acquired using equipment of such lower magnetic field strength (which is still the predominant kind of MRI system in most clinical radiology services in Brazil).

Additionally, from now onwards, it will not make sense to devise unimodal neuroimaging studies with modestly sized samples that simply attempt to replicate original findings from studies carried out in other countries. Careful definition of specific research objectives will acquire extreme importance, with the formulation of hypotheses that have never been proposed before or that would only be testable in specific populations that live in low-middle income environments. Even in such “environment-specific” neuroimaging studies, subject samples must be diligently recruited and examined in relatively short timeframes to minimize the risk of equipment and data acquisition protocols being considered of inferior quality by the time the results are submitted for publication. One particularly important strategy is to encourage close collaboration between neuroimaging labs and research groups with profound interest in specific areas of psychiatric care and privileged access to special patient populations. For instance, our psychiatric neuroimaging team was recently contacted by the specialized group dedicated to ADHD in adults also based at IPq-HCFMUSP (Programa de Deficit de Atenção e Hiperatividade no Adulto), which had started the recruitment of a unique cohort of never-treated, elderly patients with ADHD symptoms but no other cognitive deficits. This collaboration led to the publication of the first neuroimaging study of elderly individuals with ADHD worldwide, in which we used structural MRI to document regional brain volume deficits in these ADHD patients relative to elderly controls, as well as significant correlations between ADHD symptoms and volume variations in cortico-striatal-cerebellar circuits.207207. Klein M, Souza-Duran FL, Menezes AK, Alves TM, Busatto G, Louzã MR. Gray matter volume in elderly adults with ADHD: associations of symptoms and comorbidities with brain structures. J Atten Disord. 2019 Jul 2 http://www.1087054719855683 2019 Jul 2[Online ahead of print]
http://www.1087054719855683...

Brazilian neuroimaging research groups should also seize as many opportunities as possible to take part in international multigroup collaborations, as exemplified by the consortia mentioned in the previous section of this article. Our expertise to acquire and store neuroimaging databanks from large-sized samples places Brazilian groups in a privileged position to share unique data from low- and middle-income environments. Moreover, these collaborations may optimize the extraction of meaningful information from our samples, which are frequently submitted to a limited and insufficient number of analyses, thus remaining underused. Additionally, recent experience has shown that our participation in international, prospective meta-analytic investigations is a powerful means of further internationalizing research activities, fostering regular communication and networking with experts from other centers, and supplying high-quality online training for research staff. Specifically, such liaising offers vast opportunities for the assimilation of technology developed abroad, which can then be adapted and improved based on our own local needs. The open-source software ethos that is currently present in the neuroimaging community favors decentralized collaboration among researchers and may help biomedical publications to achieve a higher level of transparency, hopefully through auditability of both data and methods. Additionally, it is relevant to mention that organizers of international neuroimaging consortia are often keen to make way for Brazilian experts to share or take the lead on the testing of new hypotheses using large neuroimaging databanks acquired from subjects recruited in different parts of the world.208208. Ma Q, Zhang T, Zanetti MV, Shen H, Satterthwaite TD, Wolf DH, et al. Classification of multi-site MR images in the presence of heterogeneity using multi-task learning. Neuroimage Clin. 2018;19:476-86. Finally, the field of neuroimaging will rely increasingly more heavily on AI-based methods, and recent initiatives to create centers of excellence in AI209209. FAPESP e IBM selecionam novo Centro de Inteligência Artificial [Internet]. 2019 [cited 2019 Dec 18]. http://www.fapesp.br/13576
http://www.fapesp.br/13576...
,210210. Governo criará 8 laboratórios de inteligência artificial, diz Pontes [Internet]. 2019. [cited 2019 Dec 18]. www.poder360.com.br/governo/governo-criara-8-laboratorios-de-inteligencia-artificial-diz-pontes/
www.poder360.com.br/governo/governo-cria...
have the potential to further increase the relevance of neuroimaging research in Brazil.

One final point: we carry out research with populations frequently subjected to socioeconomic adversities

As in several other areas of neuroscience research, contemporary neuroimaging studies have provided compelling evidence that previous or current adversities, such as low socioeconomic class, low levels of educational attainment, and history of childhood maltreatment, may all reflect on interindividual variations in brain imaging measurements.211211. Gur RE, Moore TM, Rosen AF, Barzilay R, Roalf DR, Calkins ME, et al. Burden of environmental adversity associated with psychopathology, maturation, and brain behavior parameters in youths. JAMA Psychiatry. 2019;76:966-75. Investigations carried out in low- and middle-income environments must document individual information on such clinical and demographic variables, and there is a great need for neuroimaging studies evaluating specific populations subjected to adversities. These neuroimaging studies are relevant not only to increase global knowledge about the range of brain impacts derived from such conditions, but also to generate information that may be of local public health relevance.

Only a few structural MRI and fMRI investigations of this kind have been carried out in Brazil to date. One study mapped the effects of violence on anterior cingulate volumes in adults with PTSD,4747. Baldaçara L, Zugman A, Araújo C, Cogo-Moreira H, Lacerda AL, Schoedl A, et al. Reduction of anterior cingulate in adults with urban violence-related PTSD. J Affect Disord. 2014;168:13-20. while one other documented abnormalities in regional brain activity and functional connectivity patterns in preadolescents exposed to violence in an urban environment.212212. Buchweitz A, de Azeredo LA, Sanvicente-Vieira B, Cará VM, Esper NB, Soder RB, et al. Violence and Latin-American preadolescents: a study of social brain function and cortisol levels. Dev Sci. 2019;22:e12799. One additional structural MRI study of adults with bipolar disorder identified significant correlations between history of childhood maltreatment and lower volumes of brain regions that modulate emotional behavior.7878. Duarte DG, Neves Mde C, Albuquerque MR, de Souza-Duran FL, Busatto G, Corrêa H. Gray matter brain volumes in childhood-maltreated patients with bipolar disorder type I: a voxel-based morphometric study. J Affect Disord. 2016;197:74-80. Finally, a recent fMRI investigation of a large-sized population-based sample of children and adolescents reported variations in resting-state functional connectivity as a function of the quality of the family environment, involving brain regions critical to emotional processing.213213. Sato JR, Biazoli CE Jr, Salum GA, Gadelha A, Crossley N, Vieira G, et al. Associations between children's family environment, spontaneous brain oscillations, and emotional and behavioral problems. Eur Child Adolesc Psychiatry. 2019;28:835-45.

Neuroimaging findings have also been reported from a community-based sample of cognitively unimpaired elderly individuals recruited in an economically disadvantaged catchment area of São Paulo. Reductions in both regional brain volumes179179. Alves TC, Scazufca M, Squarzoni P, Duran FL, Tamashiro-Duran JH, Vallada HP, et al. Subtle gray matter changes in temporo-parietal cortex associated with cardiovascular risk factors. J Alzheimers Dis. 2011;27:575-89. and glucose metabolism214214. Tamashiro-Duran JH, Squarzoni P, Duran FL, Curiati PK, Vallada HP, Buchpiguel CA, et al. Cardiovascular risk in cognitively preserved elderlies is associated with glucose hypometabolism in the posterior cingulate cortex and precuneus regardless of brain atrophy and apolipoprotein gene variations. Age (Dordr). 2013;35:777-92. were found in direct proportion to the degree of cardiovascular risk, which is known to be significantly greater in elderly subjects with disadvantageous socioeconomic backgrounds. Additionally, silent brain infarcts were highly frequent in that sample and significantly associated with lower levels of previous education.215215. Squarzoni P, Tamashiro-Duran JH, Duran FL, Leite CC, Wajngarten M, Scazufca M, et al. High frequency of silent brain infarcts associated with cognitive deficits in an economically disadvantaged population. Clinics (Sao Paulo). 2017;72:474-80. In an additional MRI study on an expanded sample of cognitively healthy elderly individuals, variations in regional brain volumes were detected that depended on the level of previous educational attainment, supporting the notion that education may exert subtle protective effects against aging-related brain changes, in accordance with the concept of cognitive reserve.216216. Rzezak P, Squarzoni P, Duran FL, Alves TT, Tamashiro-Duran J, Bottino CM, et al. Relationship between brain age-related reduction in gray matter and educational attainment. PLoS One. 2015;10:e0140945.

The above concept of cognitive reserve is also usually invoked to explain interindividual differences in the degree of neuropathologic burden across individuals with amnestic MCI or mild AD who present comparable levels of cognitive impairment. Recent neuroimaging studies with AD and amnestic MCI samples carried out elsewhere have indicated that compensatory effects of cognitive reserve may be best documented when using sophisticated probes for specific AD-related molecular pathology indices (such as the accumulation of cortical amyloid plaques) rather than overall measures of advanced neurodegeneration (such as brain atrophy as detected with MRI).217217. Arenaza-Urquijo EM, Bejanin A, Gonneaud J, Wirth M, La Joie R, Mutlu J, et al. Association between educational attainment and amyloid deposition across the spectrum from normal cognition to dementia: neuroimaging evidence for protection and compensation. Neurobiol Aging. 2017;59:72-9. However, it is interesting to note that all contemporary neuroimaging investigations of cognitive reserve performed in other environments have recruited AD or MCI patients with 6 years of education or above.217217. Arenaza-Urquijo EM, Bejanin A, Gonneaud J, Wirth M, La Joie R, Mutlu J, et al. Association between educational attainment and amyloid deposition across the spectrum from normal cognition to dementia: neuroimaging evidence for protection and compensation. Neurobiol Aging. 2017;59:72-9. This is in contrast with our own experience of carrying out neuroimaging studies with elderly populations in Brazil, as a substantial proportion of our subjects have lower levels of educational attainment.215215. Squarzoni P, Tamashiro-Duran JH, Duran FL, Leite CC, Wajngarten M, Scazufca M, et al. High frequency of silent brain infarcts associated with cognitive deficits in an economically disadvantaged population. Clinics (Sao Paulo). 2017;72:474-80. With our recent validation and implementation of PET imaging with 11C-PiB for in vivo imaging of cortical Aβ plaques,162162. Faria DP, Duran FL, Squarzoni P, Coutinho AM, Garcez AT, Santos PP, et al. Topography of 11C-Pittsburgh compound B uptake in Alzheimer's disease: a voxel-based investigation of cortical and white matter regions. Braz J Psychiatry. 2019;41:101-11. it will be possible to assess groups of AD and MCI individuals with levels of education lower than those of all studies evaluating cognitive reserve in the international literature to date. This should allow us to directly ascertain in vivo whether elderly individuals with very low levels of education develop symptoms of dementia at a degree of cortical Aβ load that is lower than those of groups with similar levels of cognitive decline but significantly higher educational attainment and therefore greater levels of cognitive reserve. Investigations of this kind may provide clues to explain how poor educational attainment may influence increased rates of AD and earlier emergence of clinical signs of dementia in low- and middle-income countries.218218. Nitrini R, Bottino CM, Albala C, Capuñay NS, Ketzoian C, Rodriguez JJ, et al. Prevalence of dementia in Latin America: a collaborative study of population-based cohorts. Int Psychogeriatr. 2009;21:622-30.

Concluding remarks

In this article, we aimed to demonstrate how Brazilian neuroimaging research in psychiatry has achieved world-class excellence. Across various Brazilian academic centers, a number of multidisciplinary neuroimaging research teams have been formed, with the expertise to formulate and test hypotheses of worldwide and local interest in psychiatry. Liaising with radiologists, physicists, radiopharmacists, and computer data analysts, our psychiatric teams have gained access to sophisticated imaging technology, developed the capacity to acquire and analyze quality data from unique, large-sized populations, and established a tradition of collaboration both nationally and internationally with leading institutions. This has allowed our neuroimaging labs to make scientific contributions in several fronts over the past decades, including the reporting of original findings of brain changes in samples of subjects with prevalent psychiatric disorders recruited in our environment before any exposure to treatment2626. Busatto GF, Zamignani DR, Buchpiguel CA, Garrido GE, Glabus MF, Rocha ET, et al. A voxel-based investigation of regional cerebral blood flow abnormalities in obsessive-compulsive disorder using single photon emission computed tomography (SPECT). Psychiatry Res. 2000;99:15-27.,7979. Picon FA, Sato JR, Anés M, Vedolin LM, Mazzola AA, Valentini BB, et al. Methylphenidate alters functional connectivity of default mode network in drug-naive male adults with ADHD. J Atten Disord. 2020;24:447-55.; original findings of brain changes associated with subtypes of psychiatric disorders rarely or never previously evaluated in other countries2828. Skaf CR, Yamada A, Garrido GE, Buchpiguel CA, Akamine S, Castro CC, et al. Psychotic symptoms in major depressive disorder are associated with reduced regional cerebral blood flow in the subgenual anterior cingulate cortex: a voxel-based single photon emission computed tomography (SPECT) study. J Affect Disord. 2002;68:295-305.,207207. Klein M, Souza-Duran FL, Menezes AK, Alves TM, Busatto G, Louzã MR. Gray matter volume in elderly adults with ADHD: associations of symptoms and comorbidities with brain structures. J Atten Disord. 2019 Jul 2 http://www.1087054719855683 2019 Jul 2[Online ahead of print]
http://www.1087054719855683...
; the use of cross-sectional and longitudinal epidemiological designs to assess specific populations and address relationships with relevant risk factors for mental disorders8282. Axelrud LK, Santoro ML, Pine DS, Talarico F, Gadelha A, Manfro GG, et al. Polygenic risk score for Alzheimer's disease: implications for memory performance and hippocampal volumes in early life. Am J Psychiatry. 2018;175:555-63.,176176. Schaufelberger MS, Duran FL, Lappin JM, Scazufca M, Amaro E Jr, Leite CC, et al. Grey matter abnormalities in Brazilians with first-episode psychosis. Br J Psychiatry Suppl. 2007;51:s117-22.,219219. Schaufelberger MS, Lappin JM, Duran FL, Rosa PG, Uchida RR, Santos LC, et al. Lack of progression of brain abnormalities in first-episode psychosis: a longitudinal magnetic resonance imaging study. Psychol Med. 2011;41:1677-89.; development of novel intervention studies using imaging markers as outcome measures and predictors of treatment response220220. Hoexter MQ, Duran FL, D'Alcante CC, Dougherty DD, Shavitt RG, Lopes AC, et al. Gray matter volumes in obsessive-compulsive disorder before and after fluoxetine or cognitive-behavior therapy: a randomized clinical trial. Neuropsychopharmacology. 2012;37:734-45.,221221. Bulubas L, Padberg F, Bueno PV, Duran F, Busatto G, Amaro E Jr, et al. Antidepressant effects of tDCS are associated with prefrontal gray matter volumes at baseline: evidence from the ELECT-TDCS trial. Brain Stimul. 2019; 12:1197-204.; production of original findings evaluating brain effects of relevant psychopharmacological agents5757. Crippa JA, Zuardi AW, Garrido GE, Wichert-Ana L, Guarnieri R, Ferrari L, et al. Effects of cannabidiol (CBD) on regional cerebral blood flow. Neuropsychopharmacology. 2004;29:417-26.,108108. de Araujo DB, Ribeiro S, Cecchi GA, Carvalho FM, Sanchez TA, Pinto JP, et al. Seeing with the eyes shut: neural basis of enhanced imagery following Ayahuasca ingestion. Hum Brain Mapp. 2012;33:2550-60.; the use of fMRI in studies applying innovative tasks of interest to psychiatry9595. Moll J, de Oliveira-Souza R, Bramati IE, Grafman J. Functional networks in emotional moral and nonmoral social judgments. Neuroimage. 2002;16:696-703.

96. Moll J, Bado P, de Oliveira-Souza R, Bramati IE, Lima DO, Paiva FF, et al. A neural signature of affiliative emotion in the human septohypothalamic area. J Neurosci. 2012;32:12499-505.
-9797. Zahn R, Moll J, Paiva M, Garrido G, Krueger F, Huey ED, et al. The neural basis of human social values: evidence from functional MRI. Cereb Cortex. 2009;19:276-83.; publishing well-cited reviews of neuroimaging issues in top international journals222222. Freitas-Ferrari MC, Hallak JE, Trzesniak C, Santos Filho A, Machado-de-Sousa JP, Chagas MH, et al. Neuroimaging in social anxiety disorder: a systematic review of the literature. Prog Neuropsychopharmacol Biol Psychiatry. 2010;34:565-80.,223223. Ferreira LK, Busatto GF. Resting-state functional connectivity in normal brain aging. Neurosci Biobehav Rev. 2013;37:384-400.; and participation in worldwide consortia organized to analyze neuroimaging data from samples of unprecedented size.183183. van Erp TG, Walton E, Hibar DP, Schmaal L, Jiang W, Glahn DC, et al. Cortical brain abnormalities in 4474 individuals with schizophrenia and 5098 control subjects via the enhancing neuro imaging genetics through meta analysis (ENIGMA) consortium. Biol Psychiatry. 2018;84:644-54.,184184. Hibar DP, Westlye LT, Doan NT, Jahanshad N, Cheung JW, Ching CR, et al. Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group. Mol Psychiatry. 2018;23:932-42.

Additionally, we have developed awareness of the need to work in close collaboration with experts from other fields of neuroscience to devising studies that integrate neuroimaging indices with other biomarkers of interest to psychiatry. Finally, we now also work hand-in-hand with experts from computer support services in our academic centers to ensure implementation and upgrading of high-performance infrastructure for storing, transferring, and processing hundreds (or even thousands) of individual datasets, as needed to support contemporary research activities of local and interinstitutional neuroimaging consortia.

Working in a resource-limited country facing economic and political turmoil in recent years, Brazilian research groups have been under great strain, even more so in areas that depend on sophisticated technology that demands regular updating. Such a scenario is highly challenging for our neuroimaging research groups, which strive to maintain international relevance and aim to generate quality research data on the unique human populations to which we have access. In the coming years, therefore, it is of critical relevance that government funding agencies maintain their support for the research activities discussed in this paper. Also regarding funding, Brazilian groups should apply for research grants abroad more regularly, as international applications are accepted by institutions such as the National Institutes of Health, in the United States,224224. National Institutes of Health (NIH), Fogarty International Center. Information for foreign grants [Internet]. 2019. [cited 2019 Dec 20]. https://grants.nih.gov/grants/foreign/index.htm
https://grants.nih.gov/grants/foreign/in...
and private foundations such as the Brain & Behavior Research Foundation.225225. Brain & Behavior Research Foundation. Listing of grantees [Internet]. 2019 [cited 2019 dec 20]. https://www.bbrfoundation.org/about/our-people/listing-grantees
https://www.bbrfoundation.org/about/our-...
Furthermore, nurturing a culture of private sector funding in Brazil is necessary, following, for instance, the successful example of neuroimaging research sponsored by the IDOR in Rio de Janeiro. Finally, and very importantly, our universities must be able to supply a continued flow of academic career opportunities for young talents working in the field of psychiatric neuroimaging. Under favorable conditions, it may be possible to remain optimistic about our prospects of not only surviving as a relevant psychiatry research subspecialty, but also seizing new opportunities for growth in the future.

Acknowledgements

Imaging data used to generate Figure 3 were acquired with support from FAPESP grant 12/50329-6. We thank Luciana Cristina Santos for continued administrative support to the activities carried out at the Laboratório de Neuroimagem em Psiquiatria (LIM 21, HCFMUSP).

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Publication Dates

  • Publication in this collection
    08 June 2020
  • Date of issue
    Jan-Feb 2021

History

  • Received
    18 Oct 2019
  • Accepted
    3 Feb 2020
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