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ω-3 Fatty Acid Ethyl Esters Diminish Postprandial Lipemia in Familial Hypercholesterolemia.
- Source :
-
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2016 Oct; Vol. 101 (10), pp. 3732-3739. Date of Electronic Publication: 2016 Aug 04. - Publication Year :
- 2016
-
Abstract
- Context: Impaired postprandial chylomicron metabolism induces hypertriglyceridemia and may increase the risk of atherosclerotic cardiovascular disease. Omega-3 fatty acid ethyl ester (ω-3 FAEE) supplementation decreases plasma triglycerides. However, its effect on postprandial chylomicron metabolism in familial hypercholesterolemia (FH) has not yet been investigated.<br />Objective: We aimed to examine the effect of ω-3 FAEE supplementation on postprandial responses in plasma triglycerides, very-low-density lipoprotein (VLDL) apolipoprotein B (apoB)-100, and apoB-48 in FH patients receiving standard cholesterol-lowering treatment.<br />Design, Setting, and Patients: We carried out an 8-week open-label, randomized, crossover intervention trial to test the effect of oral supplementation with 4 g/d ω-3 FAEE (46% eicosapentaenoic acid and 38% docosahexaenoic acid) on postprandial triglyceride, VLDL-apoB-100, and apoB-48 responses in FH patients after ingestion of an oral fat load.<br />Outcomes Measures: Plasma total and incremental triglyceride, VLDL-apoB-100, and apoB-48 0- to 10-hour area under the curve (AUC).<br />Results: ω-3 FAEE supplementation significantly (P < .05 in all) reduced concentrations of fasting plasma triglyceride (-20%), apoB (-8%), VLDL-apoB-100 (-26%), and apoB-48 (-36%); as well as systolic blood pressure (-6%) and diastolic blood pressure (-6%). Postprandial triglyceride and VLDL-apoB-100 total AUCs (-19% and -26%, respectively; P < .01) and incremental AUCs (-18% and -35%, respectively; P < .05), as well as postprandial apoB-48 total AUC (-30%; P < .02) were significantly reduced by ω-3 FAEE supplementation.<br />Conclusion: Supplementation with ω-3 FAEEs improves postprandial lipemia in FH patients receiving standard care; this may have implications for further reducing atherosclerotic cardiovascular disease in this high-risk patient group.
- Subjects :
- Apolipoprotein B-100 blood
Apolipoprotein B-48 blood
Dietary Supplements
Docosahexaenoic Acids administration & dosage
Docosahexaenoic Acids pharmacology
Drug Therapy, Combination
Eicosapentaenoic Acid administration & dosage
Eicosapentaenoic Acid pharmacology
Fatty Acids, Omega-3 administration & dosage
Female
Humans
Hyperlipidemias blood
Hyperlipidemias etiology
Hyperlipoproteinemia Type II blood
Hyperlipoproteinemia Type II complications
Lipoproteins, VLDL blood
Male
Middle Aged
Postprandial Period
Apolipoprotein B-100 drug effects
Apolipoprotein B-48 drug effects
Fatty Acids, Omega-3 pharmacology
Hydroxymethylglutaryl-CoA Reductase Inhibitors administration & dosage
Hyperlipidemias drug therapy
Hyperlipoproteinemia Type II drug therapy
Lipoproteins, VLDL drug effects
Outcome Assessment, Health Care
Triglycerides blood
Subjects
Details
- Language :
- English
- ISSN :
- 1945-7197
- Volume :
- 101
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- The Journal of clinical endocrinology and metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 27490922
- Full Text :
- https://doi.org/10.1210/jc.2016-2217