ω-3 Polyunsaturated Fatty Acid Biomarkers and Coronary Heart Disease

Liana C. Del Gobbo(Stanford University), Fumiaki Imamura(University of Cambridge), Stella Aslibekyan(University of Alabama at Birmingham), Matti Marklund(Uppsala University), Jyrki K. Virtanen(University of Eastern Finland), Maria Wennberg(Umeå University), Mohammad Yawar Yakoob(Harvard University), Stephanie E. Chiuve(Brigham and Women's Hospital), Luicito dela Cruz(Cancer Council Victoria), Alexis C. Wood(Children's Nutrition Research Center at Baylor College of Medicine), Amanda M. Fretts(University of Washington), Eliseo Güallar(Johns Hopkins University), Chisa Matsumoto(Brigham and Women's Hospital), Kiesha Prem(National University of Singapore), Tosh Tanaka(National Institute on Aging), Jason Wu(The University of Sydney), Xia Zhou(University of Minnesota), Catherine Helmer(Inserm), Erik Ingelsson(Uppsala University), Jian‐Min Yuan(University of Pittsburgh), Pascale Barberger‐Gateau(Inserm), Hannia Campos(Harvard University), Paulo H. M. Chaves(Florida International University), Luc Djoussé(Brigham and Women's Hospital), Graham G. Giles(Cancer Council Victoria), Jose Gómez-Aracena(Universidad de Málaga), Allison Hodge(Cancer Council Victoria), Frank B. Hu(Brigham and Women's Hospital), Jan-Håkan Jansson(Umeå University), Ingegerd Johansson(Umeå University), Kay‐Tee Khaw(University of Cambridge), Woon‐Puay Koh(National University of Singapore), Rozenn N. Lemaître(University of Washington), Lars Lind(Uppsala University), Robert Luben(University of Cambridge), Eric B. Rimm(Brigham and Women's Hospital), Ulf Risérus(Uppsala University), Cécilia Samieri(Inserm), Paul W. Franks(Harvard University), David S. Siscovick(New York Academy of Medicine), Meir J. Stampfer(Brigham and Women's Hospital), Lyn M. Steffen(University of Minnesota), Brian T. Steffen(University of Minnesota), Michael Y. Tsai(University of Minnesota), Rob M. van Dam(Harvard University), Sari Voutilainen(University of Eastern Finland), Walter C. Willett(Brigham and Women's Hospital), Mark Woodward(The University of Sydney), Dariush Mozaffarian(Tufts University)
JAMA Internal Medicine
June 30, 2016
Cited by 400Open Access
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Abstract

IMPORTANCE: The role of ω-3 polyunsaturated fatty acids for primary prevention of coronary heart disease (CHD) remains controversial. Most prior longitudinal studies evaluated self-reported consumption rather than biomarkers. OBJECTIVE: To evaluate biomarkers of seafood-derived eicosapentaenoic acid (EPA; 20:5ω-3), docosapentaenoic acid (DPA; 22:5ω-3), and docosahexaenoic acid (DHA; 22:6ω-3) and plant-derived α-linolenic acid (ALA; 18:3ω-3) for incident CHD. DATA SOURCES: A global consortium of 19 studies identified by November 2014. STUDY SELECTION: Available prospective (cohort, nested case-control) or retrospective studies with circulating or tissue ω-3 biomarkers and ascertained CHD. DATA EXTRACTION AND SYNTHESIS: Each study conducted standardized, individual-level analysis using harmonized models, exposures, outcomes, and covariates. Findings were centrally pooled using random-effects meta-analysis. Heterogeneity was examined by age, sex, race, diabetes, statins, aspirin, ω-6 levels, and FADS desaturase genes. MAIN OUTCOMES AND MEASURES: Incident total CHD, fatal CHD, and nonfatal myocardial infarction (MI). RESULTS: The 19 studies comprised 16 countries, 45 637 unique individuals, and 7973 total CHD, 2781 fatal CHD, and 7157 nonfatal MI events, with ω-3 measures in total plasma, phospholipids, cholesterol esters, and adipose tissue. Median age at baseline was 59 years (range, 18-97 years), and 28 660 (62.8%) were male. In continuous (per 1-SD increase) multivariable-adjusted analyses, the ω-3 biomarkers ALA, DPA, and DHA were associated with a lower risk of fatal CHD, with relative risks (RRs) of 0.91 (95% CI, 0.84-0.98) for ALA, 0.90 (95% CI, 0.85-0.96) for DPA, and 0.90 (95% CI, 0.84-0.96) for DHA. Although DPA was associated with a lower risk of total CHD (RR, 0.94; 95% CI, 0.90-0.99), ALA (RR, 1.00; 95% CI, 0.95-1.05), EPA (RR, 0.94; 95% CI, 0.87-1.02), and DHA (RR, 0.95; 95% CI, 0.91-1.00) were not. Significant associations with nonfatal MI were not evident. Associations appeared generally stronger in phospholipids and total plasma. Restricted cubic splines did not identify evidence of nonlinearity in dose responses. CONCLUSIONS AND RELEVANCE: On the basis of available studies of free-living populations globally, biomarker concentrations of seafood and plant-derived ω-3 fatty acids are associated with a modestly lower incidence of fatal CHD.


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