APOE and the Association of Fatty Acids With the Risk of Stroke, Coronary Heart Disease, and Mortality

被引:46
作者
Satizabal, Claudia L. [1 ,3 ,4 ]
Samieri, Cecilia [5 ]
Davis-Plourde, Kendra L. [3 ,6 ]
Voetsch, Barbara [8 ]
Aparicio, Hugo J. [1 ,3 ]
Pase, Matthew P. [1 ,3 ,9 ,10 ]
Romero, Jose Rafael [1 ,3 ]
Helmer, Catherine [5 ]
Vasan, Ramachandran S. [2 ,3 ,7 ]
Kase, Carlos S. [1 ,11 ]
Debette, Stephanie [5 ,12 ]
Beiser, Alexa S. [1 ,3 ,6 ]
Seshadri, Sudha [1 ,3 ,4 ]
机构
[1] Boston Univ, Sch Med, Dept Neurol, Boston, MA 02215 USA
[2] Boston Univ, Sch Med, Dept Med, Boston, MA 02215 USA
[3] Framingham Heart Dis Epidemiol Study, Framingham, MA USA
[4] UT Hlth San Antonio, Glenn Biggs Inst Alzheimers & Neurodegenerat Dis, 7703 Floyd Curl Dr,MC 8070, San Antonio, TX 78229 USA
[5] Univ Bordeaux, INSERM, UMR U1219, Bordeaux Populat Hlth Res Ctr, Bordeaux, France
[6] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02215 USA
[7] Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02215 USA
[8] Lahey Hosp & Med Ctr, Dept Neurol, Burlington, MA USA
[9] Swinburne Univ Technol, Ctr Human Psychopharmacol, Hawthorn, Vic, Australia
[10] Florey Inst Neurosci & Mental Hlth, Melbourne Dementia Res Ctr, Parkville, Vic, Australia
[11] Emory Univ, Sch Med, Dept Neurol, Atlanta, GA 30322 USA
[12] Bordeaux Univ Hosp, Dept Neurol, Memory Clin, Bordeaux, France
基金
英国医学研究理事会;
关键词
apolipoproteins E; cardiovascular diseases; humans; lipids; mortality; MIDDLE-AGED ADULTS; APOLIPOPROTEIN-E; ISCHEMIC-STROKE; PLASMA OMEGA-3-FATTY-ACIDS; ATHEROSCLEROSIS RISK; LINOLEIC-ACID; LIPID-LEVELS; GENOTYPE; BIOMARKER; BLOOD;
D O I
10.1161/STROKEAHA.118.022132
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-The role of dietary fat on cardiovascular health and mortality remains under debate. Because the APOE is central to the transport and metabolism of lipids, we examined associations between plasma fatty acids and the risk of stroke, coronary heart disease, and mortality by APOE-epsilon 4 genotype. Methods-We included 943 FHS (Framingham Heart Study) and 1406 3C (Three-City) Bordeaux Study participants. Plasma docosahexaenoic, linoleic, arachidonic, and palmitic fatty acids were measured at baseline by gas chromatography. All-cause stroke, ischemic stroke, coronary heart disease, and all-cause mortality events were identified prospectively using standardized protocols. Each cohort used Cox models to separately relate fatty acid levels to the risk of developing each event during <= 10 years of follow-up adjusting for potential confounders and stratifying by APOE genotype (epsilon 4 carriers versus noncarriers). We then meta-analyzed summary statistics using random-effects models. Results-On average, participants had a mean age of 74 years, 61% were women, and 21% (n=483) were APOE-epsilon 4 carriers. Meta-analysis results showed that, only among APOE-epsilon 4 carriers, every SD unit increase in linoleic acid was associated with a reduced risk of all-cause stroke (hazard ratio [HR], 0.54 [95% CI, 0.38-0.78]), ischemic stroke (HR, 0.48 [95% CI, 0.33-0.71]), and all-cause mortality (HR, 0.70 [95% CI, 0.57-0.85]). In contrast, every SD unit increase in palmitic acid was related to an increased risk of all-cause stroke (HR, 1.58 [95% CI, 1.16-2.17]), ischemic stroke (HR, 1.76 [95% CI, 1.26-2.45]), and coronary heart disease (HR, 1.48 [95% CI, 1.09-2.01]), also in APOE-epsilon 4 carriers only. Results for docosahexaenoic acid and arachidonic acid were heterogeneous between cohorts. Conclusions-These exploratory results suggest that APOE-epsilon 4 carriers may be more susceptible to the beneficial or adverse impact of fatty acids on cardiovascular disease and mortality. In this subgroup, higher linoleic acid was protective for stroke and mortality, whereas palmitic acid was a risk factor for stroke and coronary heart disease. The mechanisms underlying these novel findings warrant further investigation.
引用
收藏
页码:2822 / 2829
页数:8
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