Fretts Amanda M, Mozaffarian Dariush, Siscovick David S, King Irena B, McKnight Barbara, Psaty Bruce M, Rimm Eric B, Sitlani Colleen, Sacks Frank M, Song Xiaoling, Sotoodehnia Nona, Spiegelman Donna, Lemaitre Rozenn N
Cardiovascular Health Research Unit, Epidemiology, and
Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA.
J Nutr. 2016 Feb;146(2):298-305. doi: 10.3945/jn.115.222117. Epub 2015 Dec 23.
Not much is known about the relations of circulating saturated fatty acids (SFAs), which are influenced by both metabolic and dietary determinants, with total and cause-specific mortality.
We examined the associations of plasma phospholipid SFAs with total and cause-specific mortality among 3941 older adults from the Cardiovascular Health Study, a population-based prospective study of adults aged ≥65 y who were followed from 1992 through 2011.
The relations of total and cause-specific mortality with plasma phospholipid palmitic acid (16:0), stearic acid (18:0), arachidic acid (20:0), behenic acid (22:0), and lignoceric acid (24:0) were assessed using Cox proportional hazards models.
During 45,450 person-years of follow-up, 3134 deaths occurred. Higher concentrations of the plasma phospholipid SFAs 18:0, 22:0, and 24:0 were associated with a lower risk of total mortality [multivariable-adjusted HRs (95% CIs)] for the top compared with the bottom quintile: 0.85 (0.75, 0.95) for 18:0; 0.85 (0.75, 0.95) for 22:0; and 0.80 (0.71, 0.90) for 24:0. In contrast, plasma 16:0 concentrations in the highest quintile were associated with a higher risk of total mortality compared with concentrations in the lowest quintile [1.25 (1.11, 1.41)]. We also found no association of plasma phospholipid 20:0 with total mortality.
These findings suggest that the associations of plasma phospholipid SFAs with the risk of death differ according to SFA chain length and support future studies to better characterize the determinants of circulating SFAs and to explore the mechanisms underlying these relations.
循环饱和脂肪酸(SFA)受代谢和饮食因素的影响,关于其与全因死亡率及特定病因死亡率之间的关系,目前所知甚少。
我们在心血管健康研究中,对3941名老年人血浆磷脂SFA与全因死亡率及特定病因死亡率之间的关联进行了研究。该研究是一项基于人群的前瞻性研究,研究对象为年龄≥65岁的成年人,随访时间从1992年至2011年。
采用Cox比例风险模型评估全因死亡率及特定病因死亡率与血浆磷脂棕榈酸(16:0)、硬脂酸(18:0)、花生酸(20:0)、山嵛酸(22:0)和木蜡酸(24:0)之间的关系。
在45450人年的随访期间,共发生3134例死亡。与最低五分位数相比,最高五分位数的血浆磷脂SFA 18:0、22:0和24:0浓度与较低的全因死亡风险相关[多变量调整后的HR(95%CI)]:18:0为0.85(0.75,0.95);22:0为0.85(0.75,0.95);24:0为0.80(0.71,0.90)。相比之下,最高五分位数的血浆16:0浓度与最低五分位数相比,全因死亡风险更高[1.25(1.11,1.41)]。我们还发现血浆磷脂20:0与全因死亡率之间无关联。
这些发现表明,血浆磷脂SFA与死亡风险的关联因SFA链长度而异,支持未来开展研究以更好地描述循环SFA的决定因素,并探索这些关系背后的机制。