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Effect of Marine-Derived n-3 Polyunsaturated Fatty Acids on Major Eicosanoids: A Systematic Review and Meta-Analysis from 18 Randomized Controlled Trials

BACKGROUND: Marine-derived n-3 polyunsaturated fatty acids (PUFA) may have a beneficial effect on inflammation via lowering pro-inflammatory eicosanoid concentrations. We aimed to assess the effect of marine-derived n-3 PUFA on prostaglandin E(2) (PGE(2)), thromboxane B(2) (TXB(2)), and leukotriene...

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Detalles Bibliográficos
Autores principales: Jiang, Jiajing, Li, Kelei, Wang, Fenglei, Yang, Bo, Fu, Yuanqing, Zheng, Jusheng, Li, Duo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726565/
https://www.ncbi.nlm.nih.gov/pubmed/26808318
http://dx.doi.org/10.1371/journal.pone.0147351
Descripción
Sumario:BACKGROUND: Marine-derived n-3 polyunsaturated fatty acids (PUFA) may have a beneficial effect on inflammation via lowering pro-inflammatory eicosanoid concentrations. We aimed to assess the effect of marine-derived n-3 PUFA on prostaglandin E(2) (PGE(2)), thromboxane B(2) (TXB(2)), and leukotriene B(4) (LTB(4)) through systematic review and meta-analysis of randomized controlled trials. METHOD AND FINDINGS: A structured search strategy on PubMed, Web of Science and Cochrane up to November 2015 was undertaken in this meta-analysis. Standard mean difference was used to calculate the effect size of marine-derived n-3 PUFA on PGE(2), TXB(2) and LTB(4) in a random-effect model. A total of 18 RCTs with 826 subjects were included in this systematic review and meta-analysis. Supplementation of marine-derived n-3 PUFA significantly decreased concentrations of TXB(2) in serum/plasma in subjects with high risk of cardiovascular diseases (SMD:-1.26; 95% CI: -1.65, -0.86) and LTB(4) in neutrophils in unhealthy subjects (subjects with non-autoimmune chronic diseases or auto-immune diseases) (SMD:-0.59: 95% CI: -1.02, -0.16). Subgroup analyses showed a significant reduction of LTB(4) in subjects with rheumatoid arthritis (SMD: -0.83; 95% CI: -1.37, -0.29), but not in non-autoimmune chronic disease patients (SMD: -0.33; 95% CI: -0.97, 0.31). No significant publication bias was shown in the meta-analysis. CONCLUSIONS: Marine-derived n-3 PUFA had a beneficial effect on reducing the concentration of TXB(2) in blood of subjects with high risk of CVD as well as LTB(4) in neutrophils in unhealthy subjects, and that subjects with RA showed lower LTB(4) content with supplementation of marine-derived n-3 PUFA.