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Use of Cerebrospinal Fluid for the Diagnosis of Neuroinvasive Dengue, Zika, and Chikungunya: A 19-year systematic review

Abstract

INTRODUCTION:

Cerebrospinal fluid analysis contributes to the diagnosis and neuropathogenesis of neuroinvasive arboviruses. Neurological complications caused by dengue, Zika, and chikungunya infections have high clinical relevance because of their high potential to cause death or neurological deficits. We aimed to evaluate the use of cerebrospinal fluid assays for diagnostic support in neurological disorders associated with dengue, chikungunya, and Zika infections.

METHODS:

A systematic review was carried out by searching the electronic databases LILACS, PubMed, Scopus, and Embase for articles written in English, Portuguese, or Spanish in the last 19 years. Published studies were reviewed using the terms “dengue,” “Zika”, “chikungunya”, alone or in combination with “cerebrospinal fluid” in the period from 2000 to 2019.

RESULTS:

A total of 98,060 studies were identified; of these, 1.1% (1,041 studies, 58,478 cases) used cerebrospinal fluid assays for neurological investigations. The most frequent neurological disorders included encephalitis (41.4%), congenital syndromes (17%), and microcephaly associated with Zika virus infections (8.9%). Neuroinvasive disorders were confirmed in 8.03% of 58,478 cases by specific cerebrospinal fluid analyses. The main methods used were IgM-specific antibodies (66%) and reverse transcription-polymerase chain reaction (10%). The largest number of scientific papers (29%) originated from Brazil, followed by India (18.4%) and the United States (14.4%).

CONCLUSIONS:

Although cerebrospinal fluid analysis is of great importance for increasing neurological diagnostic accuracy and contributes to the early diagnosis of neuroinvasive dengue, chikungunya, and Zika infections, it is underused in routine laboratory investigations worldwide.

Keywords:
Dengue virus; Zika virus; Chikungunya virus; Cerebrospinal fluid; Nervous system diseases

INTRODUCTION

Cerebrospinal fluid (CSF) is an ultrafiltrate of blood plasma produced by the choroid plexus cells. It protects the brain and spinal cord against trauma, provides nutrients to the nervous system tissue, and participates in the removal of residues generated by brain metabolism11. Martínez-gir R, Pantanowitz L. Cerebrospinal fluid cytology in nonmalignant aseptic meningeal disorders. Diagn Cytopathol. 2017;45(11):1020-9.,22. Heringer RR, Fernandes LEBC, Gonçalves RR, Puccioni-Sohler M. Location of injury and findings of cerebrospinal fluid in tuberculosis meningitis - Differences in the lumbar, cisternal and ventricular compartments. Arq Neuropsiquiatr. 2005;63(2B):543-7.. CSF examination dynamically reflects processes affecting the central nervous system (CNS). Analysis of the basic CSF composition (pleocytosis, mildly increased or normal protein, normal or mildly decreased glucose, and normal or mildly increased lactate levels) may contribute to the diagnosis of viral infections in the CNS33. Puccioni-Sohler M. Diagnostico de Neuroinfecção.1th ed. Rio de Janeiro: Rubio. 2008; 188 p.. Changes in these factors provide important information for the diagnosis of infectious and non-infectious neurological conditions11. Martínez-gir R, Pantanowitz L. Cerebrospinal fluid cytology in nonmalignant aseptic meningeal disorders. Diagn Cytopathol. 2017;45(11):1020-9.,22. Heringer RR, Fernandes LEBC, Gonçalves RR, Puccioni-Sohler M. Location of injury and findings of cerebrospinal fluid in tuberculosis meningitis - Differences in the lumbar, cisternal and ventricular compartments. Arq Neuropsiquiatr. 2005;63(2B):543-7.. However, CSF findings may be similar for a variety of viral agents. Therefore, accurate diagnosis depends on clinical findings and special CSF laboratory tests such as specific molecular and immunological analyses.

Arboviruses are viruses that are transmitted to the vertebrate host through the bite of arthropod vectors, especially mosquitoes and ticks, and can be maintained in wild and/or urban cycles. Among the arboviruses, the main families that cause disease in humans are the Flaviviridae, Togaviridae, and Bunyaviridae families. Flaviviruses (dengue, Zika, and yellow fever viruses) and alphaviruses (chikungunya virus) are commonly transmitted by female mosquitoes of the genus Aedes (Ae. aegypti and Ae. albopictus) in a vertebrate human viremic host44. da Silva AM, Souza AAA, Nogueira FB, Paiva IA, da Silva JC, Heringe M, et al. Main arboviruses of medical importance in Brazil: profile and diagnosis. 1th ed. Rio de Janeiro: Instituto Oswaldo Cruz. 2017; 175 p.. The broad distribution of vector mosquitoes associated with urbanization and climate change are some factors that facilitate the co-circulation of these agents, and consequently, the appearance of diseases caused by them55. Patterson J, Sammon M, Garg M. Dengue, Zika and Chikungunya: Emerging Arboviruses in the New World. West J Emerg Med. 2016;17(6):671-9..

Scientific literature has reported an increase in the occurrence of neuroinvasive diseases after the simultaneous circulation of the dengue (DENV), Zika (ZIKV), and chikungunya (CHIKV) viruses. These include neurological disturbances of high morbidity and mortality such as acute encephalitis, aseptic meningitis, myelitis, and post-infection disorders such as Guillain-Barré syndrome, acute disseminated encephalomyelitis, optic neuromyelitis, cranial nerve palsy, and congenital disorders66. Ferreira MLB, Cavalcanti CG, Coelho CA, Mesquita SD. Neurological manifestations of dengue: study of 41 cases. Arq Neuropsiquiatr . 2005;63(2B):488-93.,77. Puccioni-Sohler M, Soares CN, Papaiz-Alvarenga R, Castro MJC, Faria LC, Peralta JM. Neurologic dengue manifestations associated with intrathecal specific immune response. Neurology. 2009;73(17):1413-7.,88. Malta JM, Vargas A, Leite PL, Percio J, Coelho GE, Ferraro AHA, et al. Guillain-Barré Syndrome and other neurological manifestations possibly related to Zika virus infection in Bahia municipalities, 2015. Epidemiol Serv Saude. 2017;26(1):9-18.,99. do Rosario MS, de Jesus PA, Vasilakis N, Farias DS, Novaes MAC, Rodrigues SG, et al. Guillain-Barre Syndrome After Zika Virus Infection in Brazil. Am J Trop Med Hyg. 2016; 95(5):1157-1160.,1010. Soares CN, Brasil P, Carrera RM, Sequeira P, De Filippis AB, Borges VA, et al. Fatal encephalitis associated with Zika virus infection in an adult. J Clin Virol. 2016;83:63-5.,1111. Acevedo N, Waggoner J, Rodriguez M, Rivera L, Landivar J, Pinsky B, et al. Zika virus, chikungunya virus, and dengue virus in cerebrospinal fluid from adults with neurological manifestations, Guayaquil, Ecuador. Front Microbiol. 2017;8:42.,1212. Mehta R, Soares CN, Medialdea-Carrera R, Ellul M, da Silva MTT, Rosala-Hallas A, et al. The spectrum of neurological disease associated with Zika and chikungunya viruses in adults in Rio de Janeiro, Brazil: A case series. PLoS Negl Trop Dis. 2018;12(2):e0006212..

The diagnosis of neuroinvasive diseases associated with DENV, ZIKV, and CHIKV according to the Centers for Disease Control and Prevention (CDC) is based on the clinical criteria which include the appearance of neurological manifestations in the absence of a more likely clinical explanation, and are confirmed by laboratory criteria diagnosis, as follows: the presence of the following alone or in combination: viral RNA viral antigens in serum, CSF or other body fluids, specific IgM-reactivity in the CSF with non-reactive specific IgM reactivity for other arboviruses endemic in the region, virus-specific IgM in serum confirmed by virus-specific neutralizing antibodies, and increased titer-specific IgG in paired serum1313. Arboviral Diseases, Neuroinvasive and Non-neuroinvasive - Case Definition. [Internet]. Centers for Disease Control and Prevention guidelines; 2015 [updated 2015 January; cited 2020 Dec]. Available from: Available from: https://wwwn.cdc.gov/nndss/conditions/arboviral-diseases-neuroinvasive-and-non-neuroinvasive/case-definition/2015/
https://wwwn.cdc.gov/nndss/conditions/ar...
,1414. Ministério da Saúde (MS). Secretaria de Vigilância em Saúde. Departamento de Vigilância de Doenças Transmissiveis. Manual de Vigilância Sentinela de Doenças Neuroinvasivas por Arbovírus. 1st edition. Brasília: MS.2017;48 p.. Therefore, CSF examination has a role in demonstrating the etiological agent in viral infections of the CNS. The presence of viral genetic material in the CSF is considered to be the strongest evidence of causality33. Puccioni-Sohler M. Diagnostico de Neuroinfecção.1th ed. Rio de Janeiro: Rubio. 2008; 188 p.,1111. Acevedo N, Waggoner J, Rodriguez M, Rivera L, Landivar J, Pinsky B, et al. Zika virus, chikungunya virus, and dengue virus in cerebrospinal fluid from adults with neurological manifestations, Guayaquil, Ecuador. Front Microbiol. 2017;8:42.,1313. Arboviral Diseases, Neuroinvasive and Non-neuroinvasive - Case Definition. [Internet]. Centers for Disease Control and Prevention guidelines; 2015 [updated 2015 January; cited 2020 Dec]. Available from: Available from: https://wwwn.cdc.gov/nndss/conditions/arboviral-diseases-neuroinvasive-and-non-neuroinvasive/case-definition/2015/
https://wwwn.cdc.gov/nndss/conditions/ar...
,1515. Das T, Jaffar-Bandjee MC, Hoarau JJ, Pascale KT, Melanie D, Lee-Pat-Yuen G, et al. Chikungunya fever: CNS infection and pathologies of a re-emerging arbovirus. Prog Neurobiol. 2010;91(2):121-129.,1616. Araújo FMC, Brilhante RSN, Cavalcanti LPG, Rocha MFG, Cordeiro RA, Perdigão ACB, et al. Detection of the dengue non-structural 1 antigen in cerebral spinal fluid samples using a commercially available enzyme-linked immunosorbent assay. J Virol Methods. 2011;177(1):128-31.,1717. Puccioni-Sohler M, Rosadas C, Cabral-Castro MJ. Neurological complications in dengue infection: a review for clinical practice. Arq. Neuro-Psiquiatr. 2013;71(9B)..

The objective of this study was to conduct a review of the scientific literature on arboviruses (DENV, ZIKV, and CHIKV) that used the CSF assay for the investigation of neurological manifestations, over a period of 19 years. The results may elucidate the magnitude of CSF-assay use in arbovirus infections and demonstrate the importance of the topic; this would favor debate and interest in the scientific community about the importance of CSF assays for diagnostic support in neurological cases resulting from DENV, ZIKV, and CHIKV infections.

METHODS

Search Strategy

Published studies were reviewed using the terms “dengue”, “zika,” “chikungunya" alone and in combination with “cerebrospinal fluid” in the LILACS, PubMed, Scopus, and Embase databases. The guidelines used to report the systematic review were based on the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines1818. Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLOS Med. 2009;6(7):e1000097.. Articles written in English, Portuguese, or Spanish were selected in the period from January 1, 2000, to December 31, 2019. Articles were selected according to the presence of keywords in their titles and/or abstracts (based on the MeSH system). These documents were individually analyzed to remove duplicates in the databases. We also compared the numbers of total articles using the terms “dengue”, “Zika”, and “chikungunya” in the same 19-year period noted above. Two researchers independently searched for articles in different scientific databases and collected data, to avoid possible selection bias.

Aspects Analyzed

The articles selected for this systematic review were reviewed in detail. We analyzed the total number of publications from 2000 to 2019, the number of publications per year and country, year of publication, and publication type (e.g., case reports, short communications, original articles, reviews, etc.). We also analyzed the number of confirmed neurologic diagnoses that involved infections by DENV, ZIKV, and CHIKV that used CSF as a screening sample. From these data, we developed graphs and tables in GraphPad Prism 8.0 and/or Microsoft Office Excel 2010. We analyzed the results obtained from the databases both separately and in combination. Duplicate articles were manually deleted using the duplicate removal function of the Mendeley desktop 1.19.4 program.

RESULTS

Selected Studies

The selection process of the articles for this study is presented in the flowchart presented in the Supplementary Figure SUPPLEMENTARY MATERIAL SUPPLEMENTARY FIGURE: PRISMA chart displaying the article selection process from January 2000 to December 2019. From: Moher D, Liberati A, Tetzlaff J, Altman DG, The PRISMA Group (2009). Preferred Reporting Items for Systematic Reviews and Meta- Analyses: The PRISMA Statement. PLoS Med 6(7): e1000097. doi: 10.1371/journal.pmed1000097 For more information, visit http://www.prisma-statement.org. . A total of 1,041 (1.1%) publications out of 98,060 articles were identified from the LILACS, PubMed, Scopus, and Embase databases using the keywords “dengue”, “Zika”, “chikungunya” alone and in combination with “cerebrospinal fluid”, from January 2000 to December 2019 (Figure 1A). The use of the term “dengue” with CSF resulted in the retrieval of 20 publications from LILACS, 96 from PubMed, 332 from Scopus, and 153 from Embase, totaling 601 publications. The use of the term “Zika” with CSF resulted in the retrieval of eight publications from LILACS, 39 from PubMed, 162 from Scopus, and 30 from Embase, totaling 239 publications. The use of the term “chikungunya” with CSF resulted in the retrieval of three publications from LILACS, 35 from PubMed, 105 from Scopus, and 58 from Embase, totaling 201 publications (Figure 1B).

FIGURE 1:
Number of publications in databases by country, and confirmed diagnoses in infections by arboviruses from 2000 to 2019, retrieved using the keywords “dengue”, “Zika”, “chikungunya”, and/or “CSF”. (A) The proportion of publications using CSF for the diagnostic evaluation of the total number over these 19 years filtered using the isolated words “dengue”, “Zika”, “chikungunya” in combination with “CSF” to the total number of publications using the arbovirus terms only. (B) Number of publications in the period in the LILACS, Pubmed, Scopus, and Embase databases. (C) Total number of publications by country retrieved from the databases. Descending order of the countries with the highest scientific production according to the body of authors and collaborators. (D) Number of confirmed diagnoses involving infections by DENV, ZIKV, and CHIKV that used the cerebrospinal fluid as a screening sample, originated from the publications filtered in the databases. GBS: Guillain-Barré Syndrome; ADEM: Acute Disseminated Encephalomyelitis. SIADH: Syndrome of Inappropriate Antidiuretic Hormone. *Only arbovirus = isolated “dengue”, “Zika” “chikungunya”.

Arbovirus-specific data

A total of 98,060 publications were found in the LILACS, PubMed, Scopus, and Embase databases using the single keywords “dengue,” “Zika”, and “chikungunya”. The proportion of publications using CSF for diagnostic evaluation over these 19 years was equivalent to only 1.1% (1,041) of the DENV, ZIKV, and CHIKV arbovirus articles (Figure 1A). For each specific arbovirus, the proportion of CSF-associated publications was as follows: DENV publications, 1.0% (601/59,503), ZIKV publications, 1.1% (239/21,575), and CHIKV publications, 1.2% (201/16,982) (Figure 1A).

Principles Publication by Countries

According to the countries registered by the authors and collaborators, Brazil had the largest number of scientific papers available, accounting for 302 articles, from 2000 to 2019 (Figure 1C). This figure corresponds to 29.0% (302/1,041) of the publications. India was second with 192 publications (18.4% of 1,041), and the United States was third, with 150 publications (14.4% of 1,041) (Figure 1C).

Neurological disorders and cerebrospinal fluid assay

In the 1,041 publications selected using the keywords “dengue”, “Zika”, and “chikungunya” both alone and in combination with “cerebrospinal fluid” over the 19 years, we identified 58,478 suspected cases of arbovirus and neurological disorders such as encephalitis, congenital syndromes, microcephaly, meningoencephalitis, meningitis, GBS, and myopathy. The CSF samples were investigated for arboviruses using different methodologies such as the detection of specific IgM and/or IgG antibodies, plate reduction neutralization test, detection of viral antigens, amplification of viral RNA by PCR techniques, and next-generation metagenomic sequencing. However, only 8.03% (4,696/58,478) were confirmed as DENV, ZIKV, and/or CHIKV cases by the analysis of CSF alone or in association with other fluids (Figure 1D). The diagnosis was confirmed in 66% (3,099/4,696) of these confirmed CSF cases by the detection of specific IgM, 10% (470/4,696) by RT-PCR, 0.15% (7/4,696) by viral isolation, 0.12% (6/4,696) based on the detection of the NS1 viral protein, and 23.7% (1,114/4,696) using other methods in CSF analysis. CSF alone was used for diagnosis in 75% (3,545/4,696) of the cases, CSF and serum in 22% (1,036/4,696) , CSF, serum, and urine in 0.26% (12/4,696), CSF and urine in 0.11% (5/4,696), serum alone in 1.81% (85/4,696), and other biological specimens (saliva, amniotic fluid, and autopsy) in 0.28% (13/4,696) of the cases. Encephalitis had the highest incidence, and was reported in 41.4% of the total confirmed cases (1,944/4,696) (Figure 1D). Congenital syndromes and microcephaly were reported in 17.0% (798/4,696) and 8.9% of cases (417/4,696) respectively, and occupied the second and third positions; both of the above conditions were related to ZIKV infections, and the diagnoses were confirmed by CSF analysis (Figure 1D). GBS ranked fifth in confirmed cases, accounting for 3.7% of the total cases (174/4,696) (Figure 1D).

Publications overview

From 2000 to 2015

The number of publications that evaluated arbovirus-associated neurological manifestations in combination with CSF was low (n = 426; data not shown), considering all four databases. Except for those pertaining to DENV (341/426; data not shown), accessible works that related ZIKV (1/426; data not shown) and CHIKV (84/426; data not shown) to CSF during the reporting period were sparse.

From 2016 to 2019

There was a considerable change in the number of articles published between 2016 and 2019. In the LILACS database, 17 publications were identified: six pertaining to the keywords “dengue” and “CSF,” eight to “"Zika” and “"CSF”, and three to “chikungunya” and “CSF”. In the PubMed database, 110 publications were identified: 51 pertaining to the keywords “dengue” and “CSF”, 39 to “Zika” and “"CSF”, and 20 to “chikungunya” and “CSF”. In the Scopus database, 373 publications were identified: 152 pertaining to the keywords “dengue” and “CSF”, 161 to “Zika” and “CSF”, and 60 to “chikungunya” and “CSF”. In the Embase database, 115 publications were identified: 51 pertaining to the keywords “dengue” and “CSF”, 30 to “Zika” and “CSF”, and 34 to “chikungunya” and “CSF” (Figure 2A).

FIGURE 2:
(A) Number of publications per year from 2000 to 2019 in LILACS, Pubmed, Scopus, and Embase databases retrieved using the isolated keywords “dengue”, “Zika”, “chikungunya”, and “CSF”. (B) Numbers of types of publications from 2000 to 2019 in the LILACS, Pubmed, Scopus, and Embase databases retrieved using the isolated keywords “dengue”, Zika”, “chikungunya”, and “CSF”.

Types of publications

Regarding the types of publications, 17 original articles, 11 case reports, two reviews, and one cohort study were retrieved from the LILACS database. Querying the PubMed database resulted in the identification of 106 original articles, 37 case reports, five reviews, six case series, four cohort studies, four brief reports, four notes, two short communications, and two multicenter studies. The Scopus database filtered 441 original articles, 58 reviews, 58 letters, 21 notes, 10 editorials, seven conference papers, and two short surveys (Figure 2B). Querying the Embase database resulted in the identification of 179 original articles, 50 case reports, ten reviews, one letter, and one note. Among the most common article types, there were 743 original articles, 98 case reports, and 75 reviews.

DISCUSSION

The arboviruses DENV, ZIKV, and CHIKV are present in more than 120 subtropical and tropical countries. They emerge in poor urban areas and in the peripheral parts of the world. It is estimated that approximately 4 billion people are exposed to the risk of DENV, ZIKV, and CHIKV infections1919. Dengue Control - Epidemiology 2018. [Internet]. World Health Organization; 2018 [updated 2018 Dec; cited 2020 Dec]. Available from: Available from: https://www.who.int/denguecontrol/epidemiology/en/
https://www.who.int/denguecontrol/epidem...
. According to an epidemiological survey conducted by the Pan American Health Organization (PAHO) and the World Health Organization (WHO) in 2017, the epidemiological bulletin on DENV infection indicated a total of 579,645 reported cases, with 57,543 cases of ZIKV infections and 123,087 cases of CHIKV infections in the Americas2020. Number of Reported Cases of Chikungunya Fever in the Americas, by Country or Territory. [Internet]. Pan American Health Organization/World Health Organization; 2017 [updated 2017 Dec; cited 2020 Dec]. Available from: Available from: https://www.paho.org/hq/dmdocuments/2017/2017-dec-22-phe-CHIKV-cases-ew-51.pdf
https://www.paho.org/hq/dmdocuments/2017...
. In 2018, according to the epidemiological survey conducted by the PAHO and WHO, a total of 561,398 cases of DENV were reported, with 31,576 cases of ZIKV infections, and 94,239 cases of CHIKV infections in the Americas2121. Cases of Zika Virus Disease, by Country or Territory. [Internet]. Pan American Health Organization/World Health Organization; 2018. [updated 2018 Dec; cited 2020 Dec]. Available from: Available from: http://www.paho.org/data/index.php/en/?option=com_content&view=article&id=524:zika-weekly-en&Itemid=352
http://www.paho.org/data/index.php/en/?o...
. According to an epidemiological survey conducted by the PAHO and WHO in 2019, the epidemiological bulletin on DENV infection indicated a total of 3,140,872 reported cases, a total of 33,896 cases of ZIKV and 177,469 cases of CHIKV infections in the Americas2222. Cases of Dengue Virus Disease, by Country or Territory. [Internet]. Pan American Health Organization/World Health Organization; 2019. [updated 2019 Dec; cited 2020 Dec]. Available from: Available from: https://www.paho.org/data/index.php/en/mnu-topics/indicadores-dengue-en/dengue-nacional-en/252-dengue-pais-ano-en.html
https://www.paho.org/data/index.php/en/m...
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This study reviewed the literature that describes the presence of DENV, ZIKV, and CHIKV in the CSF in different neurological conditions (encephalitis, congenital syndromes, microcephaly, meningitis, and GBS), as reported in various types of studies (case reports, original articles, and short communications). The differences in the number of searches accessible among the databases were justified by the information obtained as a result of each of the searches. LILACS contains only Latin American data. The PubMed database comprises the medical libraries of the United States and 70 countries. Scopus is the world’s largest database and covers more than 5,000 international publishers. The Embase database has international coverage and contains more than 32 million records from more than 8,500 journals. This characteristic reflects its greater ability to filter scientific papers.

In 2015, no studies were identified in any of the analyzed databases when the keywords “Zika” and “CSF” were combined. The incidence of GBS associated with ZIKV infection increased in the epidemics of 2015 and 2016 in Brazil, Colombia, the Dominican Republic, El Salvador, Honduras, Suriname, and Venezuela2323. Campos G, Bandeira A, Sardi S. Zika Virus Outbreak, Bahia Brazil. Emerg Infect Dis. 2015;21(10):1885-6.,2424. Besnard M, Eyrolle-Guignot D, Guillemette-Artur P, Lastère S, Bost-Bezeaud F, Marcelis L, et al. Congenital cerebral malformations and dysfunction in fetuses and newborns following the 2013 to 2014 Zika virus epidemic in French Polynesia. Eurosurveillance. 2016;21(13).,2525. Cauchemez S, Besnard M, Bompard P, Dub T, Guillemette-Artur P, Eyrolle-Guignot D, et al. Association between Zika virus and microcephaly in French Polynesia, 2013-15: A retrospective study. Lancet. 2016;387(10033):2125-32.,2626. Rasmussen SA, Jamieson DJ, Honein MA, Petersen LR. Zika Virus and Birth Defects - Reviewing the Evidence for Causality. N Engl J Med. 2016;374(20):1981-7.,2727. Puccioni-Sohler M, Roveroni N, Rosadas C, Ferry F, Peralta JM, Tanuri A. Dengue infection in the nervous system: lessons learned for Zika and Chikungunya. Arq Neuropsiquiatr . 2017;75(2):123-6.. At this time, an increase in the number of microcephaly cases was recognized in Brazil during the ZIKV epidemic. This finding highlights the possible relationship between the neurological condition and infection with the virus. Retrospective studies also found a proliferation in other congenital brain abnormalities during the ZIKV epidemic in 2013 in French Polynesia2424. Besnard M, Eyrolle-Guignot D, Guillemette-Artur P, Lastère S, Bost-Bezeaud F, Marcelis L, et al. Congenital cerebral malformations and dysfunction in fetuses and newborns following the 2013 to 2014 Zika virus epidemic in French Polynesia. Eurosurveillance. 2016;21(13).,2525. Cauchemez S, Besnard M, Bompard P, Dub T, Guillemette-Artur P, Eyrolle-Guignot D, et al. Association between Zika virus and microcephaly in French Polynesia, 2013-15: A retrospective study. Lancet. 2016;387(10033):2125-32.. Therefore, the Centers for Disease Control and Prevention (CDC) confirmed this relationship based on epidemiological evidence. In February 2016, the WHO stated that the recent association of ZIKV infection with cases of microcephaly and other neurological disorders such as GBS constitutes a public health emergency of international interest, and made the notification of arboviruses such as ZIKV compulsory2828. Kindhauser MK, Allen T, Frank V, Santhana RS, Dye C. Zika: the origin and spread of a mosquito-borne virus. Bull World Health Organ. 2016;94(9):675-686C.. With this change, the growth of publications that involved these arboviruses was evident, and the co-circulation of these arboviruses became more notorious; the importance of the CSF for the neurological diagnosis of this condition was also recognized.

Brazil had the largest number of available scientific papers. Dengue fever, chikungunya fever, and acute disease caused by ZIKV are compulsory notifiable diseases in the country, and are included in the National List of Compulsory Notification of Diseases, Diseases, and Public Health Events, unified by Consolidation Ordinance No. 4 (September 28, 2017) from the Brazilian Ministry of Health. The data recorded by the Health Surveillance Secretariat demonstrate the epidemiological relevance of these arboviruses. In 2016, 2017, 2018, and 2019, the total reported probable case numbers related to DENV in various publications (1,487,924; 249,056; 247,393; 1,544,987), ZIKV (211,770; 17,338; 8,024; 10,768), and CHIKV (263,598; 185,605; 85,221; 132,205) infections in Brazil were significant2929. Ministry of Health of Brazil (MS). Monitoring of cases of dengue, chikungunya fever and fever by the Zika virus until Epidemiological Week 49. Epidemiological Bulletin. 2016;47(38):1-10.,3030. Ministry of Health of Brazil (MS). Monitoring of cases of dengue, chikungunya fever and fever by the Zika virus until Epidemiological Week 50. Epidemiological Bulletin . 2017;48(45):1-13.,3131. Ministry of Health of Brazil (MS). Monitoring of cases of dengue, chikungunya fever and fever by the Zika virus until Epidemiological Week 49. Epidemiological Bulletin . 2018;49(59):1-14.,3232. Ministry of Health of Brazil (MS). Monitoring of cases of urban arboviruses transmitted by Aedes (dengue, chikungunya and Zika), Epidemiological Weeks 01 to 52. Epidemiological Bulletin . 2019;51(2):1-16.. We demonstrated that in the same period, there was an increase in the number of publications in the databases that related arboviruses with the use of CSF for diagnosis. It is important to highlight that despite the risks inherent to patients undergoing lumbar puncture, CSF analysis may be essential for the diagnosis of infections of the central nervous system (CNS), especially in tropical countries. Knowing this relevance, in Brazil, we have a culture of doing this type of analysis, and this is reflected in the greater number of Brazilian articles using CSF samples for the diagnosis of neuroarbovirosis.

It is estimated that 0.5-21% of patients with dengue develop neurological manifestations33Carod-Artal FJ, Wichmann O, Farrar J, Gascón J. Neurological complications of dengue virus infection. Lancet Neurol. 2013;12(9):906-19.. In CHIKV infections, 16% of patients are estimated to have neurological symptoms3434. Chandak NH, Kashyap RS, Kabra D, Karandikar P, Saha SS, Morey SH, et al. Neurological complications of Chikungunya virus infection. Neurol India. 2009; 57(2):177-80.. In ZIKV infections, it is estimated that 13.4-33.3% of patients may have neurological signs 15 to 30 days after infection3535. Brito KGS, dos Santos EB, Lucas LSM, Orsini M, Fiorelli R, Teixeira S, et al. Prevalence of neurological complications associated with Zika virus in a Brazilian metropolis. Neurol Int. 2018;10(2):7638.. In a previous study, our group found 31% of cases of neuroinvasive arboviruses (DENV/CHIKV) by RT-PCR and specific IgM in the CSF and/or serum in patients with suspected infectious or post-infectious neurological disorders (encephalitis, GBS, optic neuritis, neuromyelitis optic spectrum disorder, polyneuropathy, and myelitis). This analysis showed the importance of routine CSF investigations in endemic areas3636. Mello CSM, Cabral-Castro MJ, Silva de Faria LC, Peralta JM, Puccioni-Sohler M. Dengue and chikungunya infection in neurologic disorders from endemic areas in Brazil. Neurol Clin Pract. 2020;10(6):497-502. doi: 10.1212/CPJ.0000000000000776.
https://doi.org/10.1212/CPJ.000000000000...
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The etiopathogenesis of neurological manifestations may occur through the direct action of the virus, by autoimmune mechanisms, hemorrhage, and the metabolic disorders it causes66. Ferreira MLB, Cavalcanti CG, Coelho CA, Mesquita SD. Neurological manifestations of dengue: study of 41 cases. Arq Neuropsiquiatr . 2005;63(2B):488-93.. According to the literature, encephalitis is the most common neurological manifestation of DENV infections1717. Puccioni-Sohler M, Rosadas C, Cabral-Castro MJ. Neurological complications in dengue infection: a review for clinical practice. Arq. Neuro-Psiquiatr. 2013;71(9B)., but it can also occur in ZIKV and CHIKV infections1111. Acevedo N, Waggoner J, Rodriguez M, Rivera L, Landivar J, Pinsky B, et al. Zika virus, chikungunya virus, and dengue virus in cerebrospinal fluid from adults with neurological manifestations, Guayaquil, Ecuador. Front Microbiol. 2017;8:42.. It since the 1960s, CHIKV infection has been known to affect CNS3737. Carey DE, Myers RM, Deranitz CM, Jadhav M, Reuben R. The 1964 chikungunya epidemic at Vellore, South India, including observations on concurrent dengue. Trans R Soc Trop Med Hyg. 1969;63(4):434-45.. In 2016, a cohort study was conducted at La Réunion Island reported CHIKV infections in 42% of encephalitis cases3838. Gérardin P, Couderc T, Bintner M, Tournebize P, Renouil M, Lémant J, et al. Encephalchik Study Group. Chikungunya virus-associated encephalitis: A cohort study on La Réunion Island, 2005-2009. Neurology. 2016;86(1):94-102.. We highlight here the increase in the amount of research involving congenital syndrome cases and microcephaly related to ZIKV infection, CSF-confirmed arbovirus diagnoses, and disease-related complications after the occurrence of epidemics. Similarly, from 2000 to 2019, the main confirmed neurological diagnoses related to these arboviruses were encephalitis, congenital syndromes, and microcephaly. CSF analysis is very important to diagnose newborns with congenital syndrome/microcephaly due to infection by ZIKV.

Our analysis showed that from 2000 to 2019, less than 1.1% of the scientific publications in the four databases used CSF analysis to investigate arboviruses (DENV, ZIKV, and CHIKV) in cases with neurological manifestations. As discussed above, considering the prevalence of neuroarboviruses and the importance of CSF for diagnosis, the number of scientific publications found in the area is underestimated. Therefore, neurological diseases caused by these arboviruses may be underdiagnosed. This is evident from our results which showed that only 8.03% of the suspected cases were diagnosed. Of these, 75% underwent CSF analysis alone or in association with other fluids. The detection of the specific IgM was the methodology that contributed the most to the diagnoses. Despite advances in the number of arbovirus investigations and the confirmation of CSF as an essential clinical sample in suspected cases with neurological manifestations, further research and more studies are needed. In addition, the authors do not exclude the possibility of a possible analysis bias in some of the studies included in this review. Among these biases, the sample size in the study, the statistical significance of the main result of a given study, and type of funding for some studies, may be included.

The increase in recent years in the number of cases with a co-circulation of arboviruses (for example, DENV, ZIKV, and CHIKV) worldwide has led to a continuing need for research to clarify the pathophysiology of neurovascular diseases and complications caused by arboviruses. CSF analysis contributes to the diagnostic confirmation and elucidation of the neuropathogenesis of CNS tropical neurological diseases such as arbovirus infections. CSF analysis also plays a crucial role in excluding other possible causes of neurological disorders. In cases suspected of neurological manifestations due to viral infection, neuroarboviruses should be investigated in endemic areas. Despite the high morbidity and lethality of these arboviruses and their neurological complications, we emphasize that CSF is still rarely used for elucidation, diagnostic support, and research.

ACKNOWLEDGMENTS

The authors thank Menezes, VM for their contribution to the evaluation of the work.

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  • Financial Support: Fundação Carlos Chagas de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ), Edital 18/2015 - Programa Pesquisa em Zika, Chikungunya e Dengue” for their financial support. Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) at the Post-Graduation Program in Infectious and Parasitic Diseases at Universidade Federal do Rio de Janeiro (UFRJ) for the PhD scholarship to C.Mello and FAPERJ for the Postdoctoral scholarship to M.J. Cabral-Castro.

SUPPLEMENTARY MATERIAL

SUPPLEMENTARY FIGURE:
PRISMA chart displaying the article selection process from January 2000 to December 2019.

Publication Dates

  • Publication in this collection
    28 Apr 2021
  • Date of issue
    2021

History

  • Received
    14 Jan 2021
  • Accepted
    24 Mar 2021
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