Literature DB >> 30571417

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

Claudia L Satizabal1,2,3, Cécilia Samieri4, Kendra L Davis-Plourde2,5, Barbara Voetsch6, Hugo J Aparicio1,2, Matthew P Pase1,2,7,8, José Rafael Romero1,2, Catherine Helmer4, Ramachandran S Vasan9,2,10, Carlos S Kase1,11, Stéphanie Debette4,12, Alexa S Beiser1,2,5, Sudha Seshadri1,2,3.   

Abstract

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-ε4 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 (ε4 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-ε4 carriers. Meta-analysis results showed that, only among APOE-ε4 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-ε4 carriers only. Results for docosahexaenoic acid and arachidonic acid were heterogeneous between cohorts. Conclusions- These exploratory results suggest that APOE-ε4 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.

Entities:  

Keywords:  apolipoproteins E; cardiovascular diseases; humans; lipids; mortality

Mesh:

Substances:

Year:  2018        PMID: 30571417      PMCID: PMC6310220          DOI: 10.1161/STROKEAHA.118.022132

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  35 in total

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2.  Circulating omega-6 polyunsaturated fatty acids and total and cause-specific mortality: the Cardiovascular Health Study.

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3.  Lipoprotein(a) Mass Levels Increase Significantly According to APOE Genotype: An Analysis of 431 239 Patients.

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6.  Red blood cell polyunsaturated fatty acids and mortality in the Women's Health Initiative Memory Study.

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Review 9.  Saturated fat and cardiometabolic risk factors, coronary heart disease, stroke, and diabetes: a fresh look at the evidence.

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Journal:  BMJ       Date:  2016-04-12
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  12 in total

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Review 3.  The Genetic Variability of APOE in Different Human Populations and Its Implications for Longevity.

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5.  Effects of high-fat diet and Apoe deficiency on retinal structure and function in mice.

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Review 6.  Genetic Regulatory Networks of Apolipoproteins and Associated Medical Risks.

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7.  APOE Gene Associated with Cholesterol-Related Traits in the Hispanic Population.

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8.  Lipoxins, RevD1 and 9, 13 HODE as the most important derivatives after an early incident of ischemic stroke.

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9.  The Role of DNA Methylation in Ischemic Stroke: A Systematic Review.

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10.  Sleep, major depressive disorder, and Alzheimer disease: A Mendelian randomization study.

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