n–6 fatty acid biomarkers and incident atrial fibrillation: an individual participant-level pooled analysis of 11 international prospective studies

医学 危险系数 心房颤动 前瞻性队列研究 内科学 置信区间 生物标志物 比例危险模型 队列研究 社区动脉粥样硬化风险 心脏病学 生物化学 化学
作者
Parveen K. Garg,Weihua Guan,Sarah Nomura,Natalie L. Weir,Nathan Tintle,Jyrki K. Virtanen,Yoichiro Hirakawa,Frank Qian,Qi Sun,Eric B. Rimm,Rozenn N. Lemaître,Paul N. Jensen,Susan R. Heckbert,Fumiaki Imamura,Marinka Steur,Karin Leander,Federica Laguzzi,Trudy Voortman,Toshiharu Ninomiya,Dariush Mozaffarian,William S. Harris,David S. Siscovick,Michael Y. Tsai
出处
期刊:The American Journal of Clinical Nutrition [Oxford University Press]
卷期号:118 (5): 921-929 被引量:1
标识
DOI:10.1016/j.ajcnut.2023.09.008
摘要

The presence of atrial fibrillation (AF) is associated with an over 2-fold increased risk of stroke, heart failure, and cardiovascular mortality. Long chain n–6 PUFAs have been suggested to have a variety of beneficial biologic effects that may reduce AF development; however, prior studies evaluating this relationship are limited. We prospectively evaluated the association between circulating levels of linoleic acid (LA) and arachidonic acid (AA) with incident AF. We used participant-level data from a global consortium of 11 prospective cohort studies with measurements of LA and AA in adults (aged ≥18 y). Participating studies conducted de novo analyses using a prespecified analytical plan with harmonized definitions for exposures, outcomes, covariates, and subgroups. Associations were pooled using inverse-variance weighted meta-analysis. Among 41,335 participants, 6173 incident cases of AF were ascertained, with median follow-up time of 14 y. In multivariable analysis, per interquintile range (difference between the 10th and 90th percentiles for each fatty acid), circulating n–6 levels were not associated with incident AF. For LA, the hazard ratio per interquintile range was 0.96 (95% confidence interval [CI]: 0.89, 1.04), and for AA, 1.02 (95% CI: 0.94, 1.10), with little evidence of heterogeneity between cohorts. Associations were similarly nonsignificant across subgroups of age, race, and biomarker fraction. Biomarkers of n–6 fatty acids including LA and AA are not associated with incident AF. These findings suggest that overall effects of n–6 PUFAs on influencing AF development are neutral.

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