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Metaanálisis2012Financiación no declarada

Eicosapentaenoic acid interventions in schizophrenia: meta-analysis of randomized, placebo-controlled studies

Fusar-Poli P, Berger G

Journal of clinical psychopharmacology · 76 citas

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Financiación no declarada

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Cómo se estudió

Diseño
Metaanálisis (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Financiación no declarada

Publicación

Publicado
2012-02-24 · J Clin Psychopharmacol · vol. 32 · número 2 · págs. 179–185
Editorial
Lippincott Williams & Wilkins
Citado
119 citas · más que el 99% de estudios similares · 13.7× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
31 trabajos
Acceso
De pago
Áreas de investigación
Fatty Acid Research and Health · Schizophrenia research and treatment · Tryptophan and brain disorders
Palabras clave
eicosapentaenoic acid, omega-3 fatty acids, schizophrenia, antipsychotic augmentation, psychotic symptoms, treatment-resistant psychosis, relapse prevention
MeSH
humans, eicosapentaenoic acid, treatment outcome, regression analysis, psychotic disorders, schizophrenia, dose-response relationship, drug, adult, female, male, randomized controlled trials as topic

2 autores

  • Paolo Fusar‐Poli🇬🇧 · autor de correspondenciaKing's College London
  • Gregor Emanuel Berger🇦🇺The University of Melbourne

Resumen

El texto original del estudio, en el idioma en que se publicó.

Background

Omega-3 fatty acids, in particular, eicosapentaenoic acid (EPA) have been suggested as augmentation strategies in the treatment of schizophrenia and related psychosis. Published results are conflicting, and the antipsychotic efficacy of such augmentation strategies is not well established.

Methods

Double-blind, randomized, placebo-controlled studies using purified or EPA-enriched oils in established schizophrenia were included in a meta-analysis. The effect size of EPA on psychotic symptoms was measured using Hedges' g. Publication bias was assessed with funnel plots and Egger's intercept. Heterogeneity was assessed with Q statistic and I index. Influence of moderators was assessed with meta-regression analyses in Comprehensive Meta-analysis Software version 2.

Results

The database included 167 schizophrenic subjects under the placebo arm (mean age, 37 [SD, 9.7] years; 37% females) matched with 168 schizophrenic subjects under the EPA arm (mean age, 37 [SD, 7.9] years; 36% females) (t tests P > 0.05). Meta-analysis showed no consistent significant effect for the EPA augmentation on psychotic symptoms (Hedges' g = 0.242; 95% confidence interval, 0.028-0.512, Z = 1.7531, P > 0.05). There were no significant effects for moderator variables such as age, sex, and EPA dose used in the trials. Heterogeneity across studies was small and statistically non significant (Q = 9.06; P = 0.170; I = 33.81).

Conclusions

Meta-analysis of randomized controlled trials on symptomatic outcome revealed no beneficial effect of EPA augmentation in established schizophrenia. However, no conclusion can be made for medium- to long-term effects of EPA in schizophrenia, in particular on relapse prevention in the early course of psychotic disorders.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial.

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