Harvard School of Public Health, 665 Huntington Avenue, Boston, MA 02115, USA.
Ann Intern Med. 2013 Apr 2;158(7):515-25. doi: 10.7326/0003-4819-158-7-201304020-00003.
Long-chain ω-3 polyunsaturated fatty acids (ω3-PUFAs), including eicosapentaenoic acid (EPA) (20:5ω-3), docosapentaenoic acid (DPA) (22:5ω-3), and docosahexaenoic acid (DHA) (22:6ω-3), have been shown to reduce cardiovascular risk, but effects on cause-specific and total mortality and potential dose-responses remain controversial. Most observational studies have assessed self-reported dietary intake and most randomized trials have tested effects of adding supplements to dietary intake and evaluated secondary prevention, thus limiting inference for dietary ω3-PUFAs or primary prevention.
To investigate associations of plasma phospholipid EPA, DPA, DHA, and total ω3-PUFA levels with total and cause-specific mortality among healthy older adults not receiving supplements.
Prospective cohort study.
4 U.S. communities.
2692 U.S. adults aged 74 years (±5 years) without prevalent coronary heart disease (CHD), stroke, or heart failure at baseline.
Phospholipid fatty acid levels and cardiovascular risk factors were measured in 1992. Relationships with total and cause-specific mortality and incident fatal or nonfatal CHD and stroke through 2008 were assessed.
During 30 829 person-years, 1625 deaths (including 570 cardiovascular deaths), 359 fatal and 371 nonfatal CHD events, and 130 fatal and 276 nonfatal strokes occurred. After adjustment, higher plasma levels of ω3-PUFA biomarkers were associated with lower total mortality, with extreme-quintile hazard ratios of 0.83 for EPA (95% CI, 0.71 to 0.98; P for trend = 0.005), 0.77 for DPA (CI, 0.66 to 0.90; P for trend = 0.008), 0.80 for DHA (CI, 0.67 to 0.94; P for trend = 0.006), and 0.73 for total ω3-PUFAs (CI, 0.61 to 0.86; P for trend < 0.001). Lower risk was largely attributable to fewer cardiovascular than noncardiovascular deaths. Individuals in the highest quintile of phospholipid ω3-PUFA level lived an average of 2.22 more years (CI, 0.75 to 3.13 years) after age 65 years than did those in the lowest quintile.
Temporal changes in fatty acid levels and misclassification of causes of death may have resulted in underestimated associations, and unmeasured or imperfectly measured covariates may have caused residual confounding.
Higher circulating individual and total ω3-PUFA levels are associated with lower total mortality, especially CHD death, in older adults.
National Institutes of Health.
长链 ω-3 多不饱和脂肪酸(ω3-PUFA),包括二十碳五烯酸(EPA)(20:5ω-3)、二十二碳五烯酸(DPA)(22:5ω-3)和二十二碳六烯酸(DHA)(22:6ω-3),已被证明可降低心血管风险,但对特定病因和总死亡率的影响以及潜在的剂量反应仍存在争议。大多数观察性研究评估了自我报告的饮食摄入,大多数随机试验测试了添加补充剂对饮食摄入的影响,并评估了二级预防,因此限制了对饮食 ω3-PUFA 或一级预防的推断。
研究在未服用补充剂的健康老年人中,血浆磷脂 EPA、DPA、DHA 和总 ω3-PUFA 水平与总死亡率和特定病因死亡率之间的关系。
前瞻性队列研究。
美国 4 个社区。
基线时无冠心病(CHD)、中风或心力衰竭的 2692 名美国成年人,年龄 74 岁(±5 岁)。
1992 年测量了磷脂脂肪酸水平和心血管危险因素。通过 2008 年评估与总死亡率和特定病因死亡率以及致命或非致命性 CHD 和中风事件的关系。
在 30829 人年中,有 1625 人死亡(包括 570 例心血管死亡),359 例致命性和 371 例非致命性 CHD 事件,130 例致命性和 276 例非致命性中风。调整后,ω3-PUFA 生物标志物的血浆水平较高与总死亡率降低相关,EPA 的极端五分位风险比为 0.83(95%CI,0.71 至 0.98;趋势 P 值=0.005),DPA 为 0.77(CI,0.66 至 0.90;趋势 P 值=0.008),DHA 为 0.80(CI,0.67 至 0.94;趋势 P 值=0.006),总 ω3-PUFA 为 0.73(CI,0.61 至 0.86;趋势 P 值<0.001)。较低的风险主要归因于心血管死亡人数少于非心血管死亡人数。磷脂 ω3-PUFA 水平最高五分位的个体在 65 岁后平均多活 2.22 年(CI,0.75 年至 3.13 年),而最低五分位的个体则少活 2.22 年。
脂肪酸水平的时间变化和死亡原因的错误分类可能导致低估了关联,未测量或测量不完全的协变量可能导致残留混杂。
在老年人中,较高的循环个体和总 ω3-PUFA 水平与总死亡率降低有关,尤其是 CHD 死亡。
美国国立卫生研究院。