Print version ISSN 0004-282X
Arq. Neuro-Psiquiatr. vol.67 no.3b São Paulo Sept. 2009
VIEWS AND REVIEWS
May the best friend be an enemy if not recognized early: possible role of omega-3 against cardiovascular abnormalities due antipsychotics in the treatment of autism
Pode um melhor amigo ser um inimigo se não reconhecido a tempo: possível papel do ômega-3 nos efeitos cardiovasculares secundários ao tratamento antipsicótico de pacientes com autismo
Roberta M. CysneirosI; Vera C. TerraII; Hélio R. MachadoII; Ricardo M. AridaIII; José Salomão SchwartzmanI; Esper A. CavalheiroIV, Fulvio A. ScorzaIV
IPrograma de Pós-Graduação em Distúrbios do Desenvolvimento do Centro de Ciências Biológicas e da Saúde da Universidade Presbiteriana Mackenzie, São Paulo SP, Brasil
IIDepartamento de Neurologia, Psiquiatria e Psicologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto SP, Brasil
IIIDepartamento de Fisiologia, Universidade Federal de São Paulo/Escola Paulista de Medicina (UNIFESP/EPM), São Paulo SP, Brasil
IVDisciplina de Neurologia Experimental, Universidade Federal de São Paulo/Escola Paulista de Medicina (UNIFESP/EPM), São Paulo SP, Brasil
Autism spectrum disorders (ASD) are neurodevelopment disorders that cause severe and pervasive impairment in socialization, communication, and behavior. Although the availability of antipsychotic treatment in ASD has expanded, we will be very careful with side effects of these pharmacological agents. Following this reasoning, emerging data indicate that some antipsychotics may be associated with cardiovascular adverse events (e.g., QT interval prolongation), suggesting that this could be correlated to sudden death. Quite interesting, substantial evidence from epidemiological and case-control studies indicates that omega-3 reduces the risk of cardiovascular mortality, particularly sudden cardiac death. In accordance to the above mentioned findings, as omega-3 fatty acids per se have a direct cardiovascular protective role, our paper hypothesized that omega-3 fatty acids supplementation in ASD patients treated with atypical antipsychotic drugs may reduce cardiac arrhythmias and hence sudden cardiac death.
Key words: autism spectrum disorders, heart, sudden death, omega-3.
As desordens do espectro autista (DEA) são um grupo de doenças do desenvolvimento que causam um grave comprometimento na socialização, comunicação e comportamento. Embora o tratamento na DEA com drogas antipsicóticas tenha se expandido, é necessária a observação cuidadosa de efeitos colaterais destes fármacos. Nesta linha, dados recentes têm associado o uso de antipsicóticos com efeitos adversos cardiovasculares (como prolongamento do intervalo QT), sugerindo que possa haver uma correlação com morte súbita. Evidências originadas em dados epidemiológicos e estudos de caso-controle indicam que o Omega-3 reduz o risco de mortalidade por causa cardiovascular, particularmente a morte súbita de origem cardíaca. Concordante com estes achados, como o Omega-3 per se tem um papel protetor cardiovascular direto, nosso artigo levanta a hipótese que a suplementação de ácidos graxos Omega-3 em pacientes com DEA tratados com drogas antipsicóticas podem reduzir o risco de arritmias cardíacas e assim a morte súbita cardíaca.
Palavras- chave: desordens do espectro autista, coração, morte súbita, ômega 3.
AUTISM: GENERAL ASPECTS
Autism spectrum disorders (ASD) are neurodevelopmental disorders that cause severe and pervasive impairment in socialization, communication, and behavior1,2. These include poor eye contact, deficits in other nonverbal social behaviors, social withdrawal, impaired social reciprocity, echolalia, motor stereotypes, intense and circumscribed interests, and a preoccupation with parts of objects instead of the whole1,2. These disorders are usually first diagnosed in early childhood and range from autistic disorder, through pervasive development disorder not otherwise specified, including Asperger syndrome2. The ASD are more common in the pediatric population than are some better known disorders such as diabetes, spinal bifida, or Down syndrome3. Prevalence studies have been done in different populations, including USA, United Kingdom, Europe, and Asia. A recent study of a U.S. metropolitan area estimated that 3.4 of every 1,000 children 3-10 years old had autism4. The specific cause of autism is unknown, however, evidence from twin and family studies indicates that autism is highly heritable1, neurochemical investigations have identified abnormalities in monoamines, glutamate, yamino hydroxybutyrate, and neuropeptides1,5, functional neuroimaging studies are beginning to demonstrate differences between the brains of persons with autism and those of controls1,6 and brain regions potentially involved in autism and related disorders are diverse and include the amygdale, cerebellum, fusiform gyrus, and prefrontal cortex1,7.
Although the availability of antipsychotic treatment in ASD has expanded, we should consider it very careful because of these pharmacological agents' side effects. In these way, emerging data indicate that some antipsychotics may be associated with cardiovascular adverse events (e.g., QT interval prolongation), suggesting that this could leads to torsade the points or sudden death8. Quite interesting, substantial evidence from epidemiological and case-control studies indicates that omega-3 reduces the risk of cardiovascular mortality, particularly sudden cardiac death9. In accordance to the above mentioned findings, as omega-3 fatty acids per se have a direct cardiovascular protective role9,10, we hypothesized that omega-3 fatty acids supplementation in ASD patients treated with atypical antipsychotic drugs may reduce cardiac arrhythmias and hence sudden death.
OMEGA-3 AND CARDIOVASCULAR SYSTEM: ANTIARRHYTHMIC PROPERTIES AND PREVENTION OF SUDDEN CARDIAC DEATH
The beneficial effects of omega-3 fatty acids in the cardiovascular system have been described since the seventies. Dyerberg and Bang11 demonstrated that the low prevalence of cardiac diseases in Eskimos might probably be due to high dietary ingestion of omega-3 fatty acids. In the same decade, a number of experimental studies showed an antiarrhythmic role of the omega-3 fatty acid12. In this line, McLennan and Charnock, two Australians researchers, conducted several experiments to confirm the possible antiarrhythmic role of omega-3. Initially, it was demonstrated that a dietary composed from fish oil (tuna) could prevent the ventricular fibrillation in rats induced by coronary artery occlusion following reperfusion13,14. Subsequent studies confirmed their previous data15,16. Bilman and colleagues using a sudden cardiac death model in dogs observed a reduction of arrhythmias and sudden cardiac death following ischemia induction after omega-3 administration17,18. Moreover, several works demonstrated positive effects of omega-3 in arrhythmia reduction19-23. The antiarrhythmic mechanism induced by omega-3 was modulated by Na+ and Ca2+ currents in cardiac cells24. In the same way, positive effects of omega-3 have been also observed in clinical studies. Accordingly, several studies in the nineties demonstrated that fish consumption, 1 or 2 times per week were associated to a 50% reduction of sudden cardiac death25,26. Furthermore, a clinic study for infarct prevention conducted by an Italian group (GISSI-Prevenzione), using an dose of 850 mg/day de omega-3 in 11324 subjects presenting a first myocardial infarction episode, observed a significant reduction of death caused by cardiovascular complications (30%) as well as in sudden death (45%) when compared to control subjects, suggesting an antiarrhythmic role of omega-327,28. In conclusion, human and animals studies have demonstrated a possible action of omega-3 in the prevention of cardiovascular abnormalities and reduction of occurrence of sudden cardiac death.
ATYPICAL ANTIPSYCHOTICS DRUGS, AUTISM AND CARDIOVASCULAR ABNORMALITIES
Antipsychotic therapy has become indispensable in the treatment of a variety of symptoms in ASD1 and several evidences shows that atypical antipsychotics are considered more effective than conventional antipsychotics in treating certain symptoms associated with ASD, such as aggression, irritability, and self-injurious behavior29. In these lines, the atypical antipsychotics risperidone, olanzapine, quetiapine and ziprazidone are the most commonly prescribed for ASD1,29. Concerning risperidone, several studies shows that this psychotropic atypical antipsychotic agent offers a valuable emerging option for the treatment of irritability associated with autistic disorder in children and adolescents30. Olanzapine and quetiapine have shown minimal clinical benefit in ADS based on clinical trials published at the moment1,29. Concerning ziprazidone, the use of this atypical antipsychotic in ASD remains limited, however, a single case series of 12 patients aged 8"20 years found improvements in the areas of aggression, agitation, and irritability, suggesting a future promise as a treatment for adolescents with ASD31.
In accordance to this reasoning, a pertinent question could be evaluated: should the physician pay more attention with possible cardiac abnormalities during atypical antipsychotic treatment in ASD? Although the incidence of serious adverse cardiac events in response to atypical antipsychotic medications is relatively low, some considerations should be made. For example, Ravin and Levenson described a patient who developed fatal pulseless electrical activity following initiation of risperidone therapy, suggesting that prolongation of the QTc interval with severe adverse effects remains a possibility with the use of this atypical antipsychotic32. Recently, Janion and colleagues33 reported a case of a 53 year old female with olanzapine-induced QT interval prolongation and fatal ventricular fibrillation, suggesting that all antipsychotic drugs have the potential for serious adverse events. In 2004, Kurt and Maguire called our attention about the risk of QTc interval prolongation associated with quetiapine administration34. They related a 14-year-old boy who ingested 1900 mg of quetiapine. One and one half hours after ingestion, the QTc interval lengthened from 453 msec to 618 msec on the printout (manual calculation was 444 msec to 500 msec, respectively), suggesting a relationship between higher doses of quetiapine, higher serum levels and the propensity for QTc interval prolongation. Concerning ziprasidone, Posey and co-workers1 related in an elegant review article, the potential for QTc interval prolongation with this drug on electrocardiography led to a warning in the full prescribing information. The authors suggested that ziprasidone should not be given to individuals with cardiac arrhythmias or long QT syndrome or who take other medications that can prolong the QTc interval.
CONCLUSIONS AND FUTURE REMARKS
As related before, emerging data indicate that some atypical antipsychotics prescribed for ASD may be associated with cardiovascular adverse events (e.g., QT interval prolongation), suggesting that this could leads to torsade the points or sudden death8. Although the availability of pharmacological treatment of ASD has expanded, the atypical antipsychotic drugs are still limited in clinic efficacy1. In these lines, several factors such as genetic, environmental and social can contribute to the inefficacy of therapeutic outcome patients with ASD. Among these factors, nutritional aspects, i.e., omega-3 fatty acids deficiency should also have an interesting role in this scenario. In accordance to these findings, as omega-3 fatty acids per se have a direct cardiovascular protective role (e.g., reduce serum triglycerides levels, cardiovascular disease prevention, antiarrhythmic effects, treatment after a myocardial infarction, and secondary prevention of cardiovascular disease)9,10, we believe that omega-3 fatty acids fatty acid supplementation in patients with ASD and treated with atypical antipsychotics may reduce cardiac arrhythmias and hence sudden death. In parallel, it is interesting to note that this hypothesis was evaluated by our and others research groups in schizophrenia35,36, one of the most severe forms of mental illness associated with an increased risk of cardiac sudden unexpected death and which patients make use of antipsychotics drugs. For instance, in a dose-ranging exploratory study of eicosapentaenoic acid (EPA) in 115 patients treatment-resistant schizophrenia (31 on clozapine, 48 on new atypical drugs and 36 on typical antipsychotics), subjects received 1, 2 or 4 g/day of adjunctive EPA or placebo for 12 weeks37. In patients on clozapine, a clinically important and statistically significant effect of EPA was noted (greatest effect at 2 g/day)37. Improvement correlated positively with a rise in erythrocyte arachidonic acid (AA) concentration. Additionally, clozapine-treated patients who received EPA 2 and 4 g/day showed significant reduction in triglyceride levels that were elevated previously during clozapine use37.
In the general population, clinical studies of omega-3 fatty acids have shown a reduction in sudden cardiac death, suggesting that omega-3 may have antiarrhythmic effects38. Moreover, a relationship between red blood cell (RBC) membranes omega-3 fatty acids levels and risk for sudden cardiac death have been reported as well39. Similarly, deficits in red blood cell omega-3 fatty acids have been reported in medicated psychotic subjects41,49. Quite interesting, compelling evidence was found that a low dietary of omega-3 fatty acids in conjunction with sedentary behavior and mental stress combined with various personality traits can enhance sympathetic activity and increase the secretion of catecholamine, cortisol and serotonin, all of which appear to be underlying mechanisms involved in metabolic syndrome42, a potentially catastrophic multiplex risk factor for cardiovascular disease and hence sudden cardiac death in patients prescribed with antipsychotic drugs.
Concerning specifically the pediatric population, Vancassel et al. in an elegant study demonstrated a reduction in polyunsaturated fatty acids and aracdonic acids in ASD and in mentally retarded patients, when compared to normal patients. Similar variations have been described in other psychiatric diseases, such as schizophrenia, attention deficit and hyperactivity disease, major depression and bipolar disorders, compared to control subjects43. The authors proposes this could represent an additional approach to the treatment of autism, through polyunsaturated fatty acids dietary supplementation43. Other authors, in a pilot study suggested the effectiveness of fish oil supplementation to reduce hyperactivity in 12 children with ASD. Considering this data together, it seems that polyunsaturated fatty acids serum levels may play an important role in the mechanisms of development of behavioral diseases44.
Where do we go from here? We are sure that more needs to be done and on the basis of laboratory data and clinical findings, there are reasons to suggest that omega-3 may offer a host of benefits to people with ASD. As we know, omega-3 fatty acids are long-chain, polyunsaturated fatty acids found in plant and marine sources45 (Table). Actually, it has long been believed that a daily intake of 3000 to 4000 mg of fish oil supplements or 2 to 3 servings of fatty fish per week are safe and effective to adults in general, included those with psychiatric disorders45. In this way, new considerations and experimental, epidemiological and clinical studies should be evaluated to establish with precision the relationship between omega 3 fatty acids, atypical antipsychotic and ASD.
1. Posey DJ, Stigler KA, Erickson CA, McDougle CJ. Antipsychotics in the treatment of autism. J Clin Invest 2008;118:6-14. [ Links ]
2. National Institute of Mental Health. Autism Spectrum Disorders (Pervasive Developmental Disorders) 2008. http://www.nimh.nih.gov/health/topics/autism-spectrum-disorders-pervasive-developmental-disorders/index.shtml. [ Links ]
3. Filipek PA, Accardo PJ, Baranek GT, et al. The screening and diagnosis of autism spectrum disorders. J Autism Dev Disord 1999;29:439-484. [ Links ]
4. Yeargin-Allsopp M, Rice C, Karapurkar T, Doernberg N, Boyle C, Murphy C. Prevalence of autism in a US metropolitan area. JAMA 2003;289: 49-55. [ Links ]
5. McDougle CJ, Erickson CA, Stigler KA, Posey DJ. Neurochemistry in the pathophysiology of autism. J Clin Psychiatry 2005;66(Suppl 10):S9-S18. [ Links ]
6. DiMartino A, Castellanos FX. Functional neuroimaging of social cognition in pervasive developmental disorders: a brief review. Ann N Y Acad Sci 2003;1008:256-260. [ Links ]
7. Mercadante MT, Cysneiros RM, Schwartzman JS, Arida RM, Cavalheiro EA, Scorza FA. Neurogenesis in the amygdala: a new etiologic hypothesis of autism? Med Hypotheses 2008;70:352-357. [ Links ]
8. Straus SM, Bleumink GS, Dieleman JP, et al. Antipsychotics and the risk of sudden cardiac death. Arch Intern Med 2004;164:1293-1297. [ Links ]
9. Calder PC. n-3 fatty acids and cardiovascular disease: evidence explained and mechanisms explored. Clin Sci 2004;107:1-11. [ Links ]
10. von Schacky C, Omega-3 fatty acids and cardiovascular disease. Curr Opin Clin Nutr Metab Care 2007;10:129-135. [ Links ]
11. Dyerberg J, Bang HO. Haemostatic function and platelet polyunsaturated fatty acids in Eskimos. Lancet 1979;2:433-435. [ Links ]
12. Gudbjarnason S, Hallgrimsson J. Prostaglandins and polyunsaturated fatty acids in heart muscle. Acta Biol Med Ger 1976;35:1069-1080. [ Links ]
13 McLennan PL, Bridle TM, Abeywardena MY, Charnock JS. Dietary lipid modulation of ventricular fibrillation threshold in the marmoset monkey. Am Heart J 1992;123:1555-1561. [ Links ]
14. McLennan PL. Relative effects of dietary saturated, monounsaturated, and polyunsaturated fatty acids on cardiac arrhythmias in rats. Am J Clin Nutr 1993;57:207-212. [ Links ]
15. Yang BC, Saldeen TG, Bryant JL, Nichols WW, Mehta JL. Long-term dietary fish oil supplementation protects against ischemia-reperfusion-induced myocardial dysfunction in isolated rat hearts. Am Heart J 1993;126:1287-1292. [ Links ]
16. Jacobsen AN, Du XJ, Dart AM, Woodcock EA. Ins(1,4,5)P3 and arrhythmogenic responses during myocardial reperfusion: evidence for receptor specificity. Am J Physiol 1997;273:1119-1125. [ Links ]
17. Billman GE, Hallaq H, Leaf A. Prevention of ischemia-induced ventricular fibrillation by omega 3 fatty acids. Proc Natl Acad Sci USA 1994;91: 4427-4430. [ Links ]
18. Billman GE, Kang JX, Leaf A. Prevention of ischemia-induced cardiac sudden death by n-3 polyunsaturated fatty acids in dogs. Lipids 1997; 32:1161-1168. [ Links ]
19. Kang JX, Leaf A. Effects of long-chain polyunsaturated fatty acids on the contraction of neonatal rat cardiac myocytes. Proc Natl Acad Sci USA 1994;91:9886-9890. [ Links ]
20. Kang JX, Leaf A. Antiarrhythmic effects of polyunsaturated fatty acids. Recent studies. Circulation 1996;94:1774-1780. [ Links ]
21. Xiao YF, Kang JX, Morgan JP, Leaf A. Blocking effects of polyunsaturated fatty acids on Na+ channels of neonatal rat ventricular myocytes. Proc Natl Acad Sci USA 1995;92:11000-11004. [ Links ]
22. Xiao YF, Gomez AM, Morgan JP, Lederer WJ, Leaf A. Suppression of voltage-gated L-type Ca2+ currents by polyunsaturated fatty acids in adult and neonatal rat ventricular myocytes. Proc Natl Acad Sci USA 1997;94:4182-4187. [ Links ]
23. Xiao YF, Wright SN, Wang GK, Morgan JP, Leaf A. Coexpression with beta(1)-subunit modifies the kinetics and fatty acid block of hH1(alpha) Na(+) channels. Am J Physiol Heart Circ Physiol 2000;279:35-46. [ Links ]
24. Leaf A, Kang JX, Xiao YF, Billman GE. Clinical prevention of sudden cardiac death by n-3 polyunsaturated fatty acids and mechanism of prevention of arrhythmias by n-3 fish oils. Circulation 2003;107: 2646-2652. [ Links ]
25. Albert CM, Hennekens CH, O'Donnell CJ, et al. Fish consumption and risk of sudden cardiac death. JAMA 1998;279:23-28. [ Links ]
26. Siscovick DS, Lemaitre RN, Mozaffarian D. The fish story: a diet-heart hypothesis with clinical implications: n-3 polyunsaturated fatty acids, myocardial vulnerability, and sudden death. Circulation 2003;107:2632-2634. [ Links ]
27. Marchioli R. Results of GISSI prevenzione: diet, drugs, and cardiovascular risk. Researchers of GISSI Prevenzione. Cardiologia 1999;44: 745-746. [ Links ]
28. Marchioli R, Barzi F, Bomba E, et al. and AMD GISSI-Prevenzione Investigators. Early protection against sudden death by n-3 polyunsaturated fatty acids after myocardial infarction: time-course analysis of the results of the Gruppo Italiano per lo Studio della Sopravvivenza nell'Infarto Miocardico (GISSI)-Prevenzione. Circulation 2002;105:1897-1903. [ Links ]
29. Chavez B, Chavez-Brown M, Sopko MA Jr, Rey JA. Atypical antipsychotics in children with pervasive developmental disorders. Paediatr Drugs 2007;9:249-266. [ Links ]
30. Scott LJ, Dhillon S. Risperidone: a review of its use in the treatment of irritability associated with autistic disorder in children and adolescents. Paediatr Drugs. 2007;9:343-354. [ Links ]
31. McDougleCJ, KimDL, PoseyDJ. Case series: use of ziprasidone for maladaptive symptoms in youths with autism. J Amer Acad Child Adolescent Psychiatry 2002;41:921-927. [ Links ]
32. Ravin DS, Levenson JW. Fatal cardiac event following initiation of risperidone therapy. Ann Pharmacother 1997;31:867-870. [ Links ]
33. Glassman AH, Bigger JTJ. Antipsychotic drugs: prolonged QTc interval, torsade de pointes, and sudden death. Am J Psychiatry 2001;158: 1774-1782. [ Links ]
34. Kurth J, Maguire G. Pediatric case report of quetiapine overdose and QTc prolongation. Ann Clin Psychiatry 2004;16:229-231. [ Links ]
35. Scorza FA, Mari JJ, Bressan RA. Sudden cardiac death in schizophrenia: should the psychiatrist pay more attention? Rev Bras Psiquiatr 2006; 28:339. [ Links ]
36. Glassman AH. Schizophrenia, antipsychotic drugs, and cardiovascular disease. J Clin Psychiatry. 2005;66(Suppl6):S5-S10. [ Links ]
37. Peet M, Horrobin DF, E-E Multicentre Study Group. A dose ranging exploratory study of the effects of ethyl eicosapentaenoate in patients with persistent schizophrenic symptoms. J Psychiatr Res 2002;36:7-18. [ Links ]
38. Raitt MH, Connor WE, Morris C, J Fish oil supplementation and risk of ventricular tachycardia and ventricular fibrillation in patients with implantable defibrillators: a randomized controlled trial. JAMA 2005;293: 2884-2891. [ Links ]
39. Harris WS, von Schacky C. The Omega-3 Index: a new risk factor for death from coronary heart disease? Prev Med 2004;39:212-220. [ Links ]
40. Yao JK, van Kammen DP, Welker JA. Red blood cell membrane dynamics in schizophrenia. II. Fatty acid composition. Schizophr Res 1994;13: 217-226. [ Links ]
41. Yao JK, van Kammen DP, Gurklis J. Red blood cell membrane dynamics in schizophrenia. III. Correlation of fatty acid abnormalities with clinical measures. Schizophr Res 1994;13:227-232. [ Links ]
42. Singh RB, Pella D, Mechirova V, Otsuka K. Can brain dysfunction be a predisposing factor for metabolic syndrome? Biomed Pharmacother 2004;58:(Suppl). S56-S68. [ Links ]
43. Vancassel S, Durand G, Barthe C, B, J, D, C, S. Plasma fatty acid levels in autistic children. Prostaglandins, Leukotrienes Essential FattyAcids 2001;65:1-7. [ Links ]
44. Amminger GP, Berger GE, Scha¨fer MR, Klier C, Friedrich MH, Feucht M. Omega-3 fatty acids supplementation in children with autism: a double-blind randomized, placebo-controlled pilot study. Biol Psychiatry 2007;61:551-553. [ Links ]
45. Mazza M, Pomponi M, Janiri L, Bria P, Mazza S. Omega-3 fatty acids and antioxidants in neurological and psychiatric diseases: an overview. Prog. Neuropsychopharmacol Biol Psychiatry 2007;31:12-26. [ Links ]
Received 10 February 2009, received in final form 14 July 2009. Accepted 1 August 2009.
Financial support: FAPESP, CNPq, CInAPCe-FAPESP and FAEPA.
Dra. Vera Cristina Terra - Department of Neurology / CIREP / Campus Universitário - 14048-900 Ribeirão Preto SP - Brasil. E-mail: firstname.lastname@example.org