Cardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, WA 98101, USA.
Metabolism. 2010 Jul;59(7):1029-34. doi: 10.1016/j.metabol.2009.10.026. Epub 2009 Dec 31.
Little is known of the associations of endogenous fatty acids with sudden cardiac arrest (SCA). We investigated the associations of SCA with red blood cell membrane fatty acids that are end products of de novo fatty acid synthesis: myristic acid (14:0), palmitic acid (16:0), palmitoleic acid (16:1 n7), vaccenic acid (18:1 n7), stearic acid (18:0), oleic acid (18:1 n9), and a related fatty acid, cis-7 hexadecenoic acid (16:1 n9). We used data from a population-based case-control study where cases, aged 25 to 74 years, were out-of-hospital SCA patients attended by paramedics in Seattle, WA (n = 265). Controls, matched to cases by age, sex, and calendar year, were randomly identified from the community (n = 415). All participants were free of prior clinically diagnosed heart disease. We observed associations of higher red blood cell membrane levels of 16:0, 16:1n-7, 18:1n-7, and 16:1n-9 with higher risk of SCA. In analyses adjusted for traditional SCA risk factors and trans- and n-3 fatty acids, a 1-SD-higher level of 16:0 was associated with 38% higher risk of SCA (odds ratio, 1.38; 95% confidence interval, 1.12-1.70) and a 1-SD-higher level of 16:1n-9 with 88% higher risk (odds ratio, 1.88; 95% confidence interval, 1.27-2.78). Several fatty acids that are end products of fatty acid synthesis are associated with SCA risk. Further work is needed to investigate if conditions that favor de novo fatty acid synthesis, such as high-carbohydrate/low-fat diets, might also increase the risk of SCA.
关于内源性脂肪酸与心搏骤停(SCA)之间的关联,我们知之甚少。我们研究了 SCA 与红细胞膜脂肪酸之间的关联,这些脂肪酸是从头合成脂肪酸的终产物:肉豆蔻酸(14:0)、棕榈酸(16:0)、棕榈油酸(16:1 n7)、反式 11-十八碳烯酸(18:1 n7)、硬脂酸(18:0)、油酸(18:1 n9)和一种相关脂肪酸,顺-7 十六碳烯酸(16:1 n9)。我们使用了一项基于人群的病例对照研究的数据,该研究中的病例为年龄在 25 至 74 岁之间的院外 SCA 患者,由西雅图的护理人员进行治疗(n=265)。对照组通过年龄、性别和日历年份与病例相匹配,从社区中随机抽取(n=415)。所有参与者均无先前临床诊断的心脏病。我们观察到红细胞膜中 16:0、16:1n-7、18:1n-7 和 16:1n-9 水平升高与 SCA 风险增加相关。在调整了传统 SCA 风险因素以及反式和 n-3 脂肪酸后,16:0 水平每升高 1-SD,SCA 的风险增加 38%(比值比,1.38;95%置信区间,1.12-1.70),16:1n-9 水平每升高 1-SD,SCA 的风险增加 88%(比值比,1.88;95%置信区间,1.27-2.78)。几种是脂肪酸合成终产物的脂肪酸与 SCA 风险相关。需要进一步研究以确定是否有利于从头合成脂肪酸的条件,如高碳水化合物/低脂肪饮食,也可能增加 SCA 的风险。