Chan Dick C, Pang Jing, Barrett P Hugh R, Sullivan David R, Burnett John R, van Bockxmeer Frank M, Watts Gerald F
School of Medicine and Pharmacology (D.C.C., J.P., P.H.R.B., J.R.B., G.F.W.), Faculty of Engineering, Computing, and Mathematics (P.H.R.B.), and School of Surgery (F.M.v.B.), University of Western Australia, Perth, Western Australia 6847, Australia; Department of Clinical Biochemistry (D.R.S.), Royal Prince Alfred Hospital, Camperdown, New South Wales 2050, Australia; and Department of Clinical Biochemistry (J.R.B., F.M.v.B.), PathWest Laboratory Medicine, Royal Perth Hospital and Fiona Stanley Hospital Network, Perth, Western Australia 6000, Australia.
J Clin Endocrinol Metab. 2016 Oct;101(10):3732-3739. doi: 10.1210/jc.2016-2217. Epub 2016 Aug 4.
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.
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.
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.
Plasma total and incremental triglyceride, VLDL-apoB-100, and apoB-48 0- to 10-hour area under the curve (AUC).
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.
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.
餐后乳糜微粒代谢受损会导致高甘油三酯血症,并可能增加动脉粥样硬化性心血管疾病的风险。补充ω-3脂肪酸乙酯(ω-3 FAEE)可降低血浆甘油三酯水平。然而,其对家族性高胆固醇血症(FH)患者餐后乳糜微粒代谢的影响尚未得到研究。
我们旨在研究在接受标准降胆固醇治疗的FH患者中,补充ω-3 FAEE对餐后血浆甘油三酯、极低密度脂蛋白(VLDL)载脂蛋白B(apoB)-100和apoB-48反应的影响。
设计、地点和患者:我们进行了一项为期8周的开放标签、随机、交叉干预试验,以测试每日口服4 g ω-3 FAEE(46%二十碳五烯酸和38%二十二碳六烯酸)对FH患者口服脂肪负荷后餐后甘油三酯、VLDL-apoB-100和apoB-48反应的影响。
血浆总甘油三酯和增量甘油三酯、VLDL-apoB-100以及apoB-48在0至10小时的曲线下面积(AUC)。
补充ω-3 FAEE后,空腹血浆甘油三酯浓度(-20%)、apoB(-8%)、VLDL-apoB-100(-26%)和apoB-48(-36%)均显著降低(所有P值均<0.05);收缩压(-6%)和舒张压(-6%)也显著降低。补充ω-3 FAEE后,餐后甘油三酯和VLDL-apoB-100的总AUC(分别为-19%和-26%;P<0.01)和增量AUC(分别为-18%和-35%;P<0.05),以及餐后apoB-48总AUC(-30%;P<0.02)均显著降低。
在接受标准治疗的FH患者中,补充ω-3 FAEE可改善餐后血脂异常;这可能对进一步降低该高危患者群体的动脉粥样硬化性心血管疾病风险具有重要意义。