Metabolic Research Centre, School of Medicine and Pharmacology, University of Western Australia, Perth, Australia.
Diabetes Care. 2009 Nov;32(11):2111-3. doi: 10.2337/dc09-0519. Epub 2009 Aug 3.
Subjects with the metabolic syndrome have reduced HDL cholesterol concentration and altered metabolism of high-density lipoprotein (Lp)A-I and LpA-I:A-II particles. In the metabolic syndrome, fenofibrate and atorvastatin may have differential effects on HDL particle kinetics.
Eleven men with metabolic syndrome were studied in a randomized, double-blind, crossover trial of 5-week intervention periods with placebo, fenofibrate (200 mg/day), and atorvastatin (40 mg/day). LpA-I and LpA-I:A-II kinetics were examined using stable isotopic techniques and compartmental modeling.
Compared with placebo, fenofibrate significantly increased the production of both LpA-I:A-II (30% increase; P < 0.001) and apoA-II (43% increase; P < 0.001), accounting for significant increases of their corresponding plasma concentrations (10 and 23% increases, respectively), but it did not alter LpA-I kinetics or concentration. Atorvastatin did not significantly alter HDL concentration or the kinetics of HDL particles.
In the metabolic syndrome, fenofibrate, but not atorvastatin, influences HDL metabolism by increasing the transport of LpA-I:A-II particles.
患有代谢综合征的受试者高密度脂蛋白(HDL)胆固醇浓度降低,高密度脂蛋白(Lp)A-I 和 LpA-I:A-II 颗粒的代谢发生改变。在代谢综合征中,非诺贝特和阿托伐他汀可能对 HDL 颗粒动力学有不同的影响。
11 名患有代谢综合征的男性参加了一项随机、双盲、交叉试验,为期 5 周的干预期分别使用安慰剂、非诺贝特(200mg/天)和阿托伐他汀(40mg/天)。使用稳定同位素技术和房室模型研究了 LpA-I 和 LpA-I:A-II 的动力学。
与安慰剂相比,非诺贝特显著增加了 LpA-I:A-II 的产生(增加 30%;P<0.001)和载脂蛋白 A-II 的产生(增加 43%;P<0.001),导致其相应血浆浓度显著增加(分别增加 10%和 23%),但不改变 LpA-I 动力学或浓度。阿托伐他汀对 HDL 浓度或 HDL 颗粒动力学没有显著影响。
在代谢综合征中,非诺贝特而非阿托伐他汀通过增加 LpA-I:A-II 颗粒的转运来影响 HDL 代谢。