罗格列酮和非诺贝特对血脂的累加作用。

Cholesterol Pub Date : 2011-01-01 Epub Date: 2011-11-24 DOI:10.1155/2011/286875
Ahmad Slim, Laudino Castillo-Rojas, Eddie Hulten, Jennifer N Slim, Dorette Pearce Moore, Todd C Villines
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引用次数: 3

摘要

背景。评价罗格列酮、非诺贝特或两者联合使用对血糖正常的健康成人血脂的影响。方法与结果。受试者以双盲方式随机分为罗格列酮+安慰剂、非诺贝特+安慰剂、罗格列酮+非诺贝特或匹配的双安慰剂。比较治疗12周后空腹TG、高密度脂蛋白胆固醇(HDL-C)、LDL-C及血浆载脂蛋白A-I、A-II、C-III水平变化的组间差异。共筛选548名受试者,其中41名符合纳入标准。治疗12周后,与安慰剂组相比,单用非诺贝特组和罗格列酮/非诺贝特组甘油三酯水平的中位数变化显示显著降低,范围从47到55毫克/分升(P = 0.0496)。然而,仅罗格列酮组甘油三酯水平没有明显变化。与安慰剂组相比,所有治疗组Apo AII的变化均有所增加(P = 0.009)。非诺贝特组和罗格列酮/非诺贝特组Apo CIII水平也有显著变化(P = 0.0003)。结论。罗格列酮似乎不能调节独立于葡萄糖代谢的甘油三酯升高患者的高甘油三酯血症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rosiglitazone and fenofibrate additive effects on lipids.

Rosiglitazone and fenofibrate additive effects on lipids.

Rosiglitazone and fenofibrate additive effects on lipids.

Background. To evaluate the effect of rosiglitazone, fenofibrate, or their combined use on plasma lipids in normoglycemic healthy adults. Methods and Results. Subjects were randomized in a double-blind fashion to rosiglitazone + placebo, fenofibrate + placebo, rosiglitazone + fenofibrate, or matching double placebo. The between-group difference in the change in fasting TG, high-density lipoprotein cholesterol (HDL-C), LDL-C, and plasma apolipoproteins A-I, A-II, and C-III level were compared after 12 weeks of treatment. A total of 548 subjects were screened and 41 met the inclusion criteria. After 12 weeks of therapy, the median change in the triglyceride levels showed a significant reduction ranging from 47 to 55 mg per deciliter in the fenofibrate only and rosiglitazone/fenofibrate groups compared with placebo (P = 0.0496). However, the rosiglitazone only group did not show significant change in triglyceride level. The change in the Apo AII showed increase in all the treatment groups compared with placebo (P = 0.009). There was also significant change in the Apo CIII that showed reduction of its level in the fenofibrate only and rosiglitazone/fenofibrate groups (P = 0.0003). Conclusion. Rosiglitazone does not appear to modulate hypertriglyceridemia in patients with elevated triglycerides independent of glucose metabolism.

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