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在2型糖尿病治疗中,吡格列酮与格列齐特加二甲双胍相比以及吡格列酮与磺脲类加二甲双胍相比,对脂质和脂蛋白的长期影响。

Long-term effects on lipids and lipoproteins of pioglitazone versus gliclazide addition to metformin and pioglitazone versus metformin addition to sulphonylurea in the treatment of type 2 diabetes.

作者信息

Betteridge D J, Vergès B

机构信息

Department of Medicine, University College London, Sir Jules Thorn Institute, The Middlesex Hospital, 5th Floor, Mortimer Street, London, W1N 8AA, UK.

出版信息

Diabetologia. 2005 Dec;48(12):2477-81. doi: 10.1007/s00125-005-0034-1. Epub 2005 Nov 10.

Abstract

AIMS/HYPOTHESIS: The aim of this study was to determine the long-term effects of pioglitazone add-on to metformin or sulphonylurea on plasma lipids and lipoproteins.

MATERIALS AND METHODS

The effects of pioglitazone were studied in two clinical trials in patients with inadequately controlled type 2 diabetes (HbA1c > or =7.5 and < or =11%). In the first trial, patients currently receiving metformin were randomised to pioglitazone (15-45 mg/day, n=317) or gliclazide (80-320 mg/day, n=313) add-on therapy. In the second study, pioglitazone (15-45 mg/day, n=319) or metformin (850-2,550 mg/day, n=320) was added to sulphonylurea therapy. Patients were force-titrated to the maximum tolerated dose of add-on therapy, which was maintained to the 2-year endpoint.

RESULTS

There were no statistically significant differences between the groups with respect to HbA1c reduction from baseline to week 104. Whether added to metformin or sulphonylurea, pioglitazone caused highly significant greater decreases in triglycerides and increases in HDL cholesterol from baseline to week 104 than treatments with gliclazide or metformin add-on therapies (p< or =0.001). The triglyceride reductions noted with pioglitazone were maintained over time, with decreases of 16-18% at 1 year and 17-23% at 2 years. In the pioglitazone groups, the improvement in HDL cholesterol at 1 year was maintained, with 21-22% augmentations at 2 years (p<0.001 between-group difference). Small but statistically significant greater reductions in LDL cholesterol were observed with gliclazide vs pioglitazone add-on to metformin and metformin vs pioglitazone add-on to sulphonylurea (p<0.001 for between-group difference). In the pioglitazone groups, mean LDL cholesterol at 2 years was similar to mean baseline LDL cholesterol.

CONCLUSIONS/INTERPRETATION: After 2 years, highly significant decreases in triglycerides and increases in HDL cholesterol that were sustained over time or even improved were observed when pioglitazone was added to metformin or sulphonylurea therapy. These effects of pioglitazone on lipids may be potentially beneficial in reducing cardiovascular risk in type 2 diabetes.

摘要

目的/假设:本研究旨在确定吡格列酮联合二甲双胍或磺脲类药物对血脂和脂蛋白的长期影响。

材料与方法

在两项针对2型糖尿病控制不佳(糖化血红蛋白≥7.5%且≤11%)患者的临床试验中研究了吡格列酮的作用。在第一项试验中,将目前正在接受二甲双胍治疗的患者随机分为接受吡格列酮(15 - 45毫克/天,n = 317)或格列齐特(80 - 320毫克/天,n = 313)的联合治疗组。在第二项研究中,将吡格列酮(15 - 45毫克/天,n = 319)或二甲双胍(850 - 2550毫克/天,n = 320)添加到磺脲类药物治疗中。患者被强制滴定至联合治疗的最大耐受剂量,并维持至2年终点。

结果

从基线到第104周,各治疗组间糖化血红蛋白降低幅度无统计学显著差异。无论添加到二甲双胍还是磺脲类药物中,与格列齐特或二甲双胍联合治疗相比,吡格列酮从基线到第104周导致甘油三酯显著降低且高密度脂蛋白胆固醇显著升高(p≤0.001)。吡格列酮引起的甘油三酯降低随时间持续存在,1年时降低16 - 18%,2年时降低17 - 23%。在吡格列酮组中,1年时高密度脂蛋白胆固醇的改善得以维持,2年时升高21 - 22%(组间差异p<0.001)。与二甲双胍联合吡格列酮及磺脲类药物联合吡格列酮相比,格列齐特联合二甲双胍及二甲双胍联合磺脲类药物导致低密度脂蛋白胆固醇降低幅度虽小但有统计学显著差异(组间差异p<0.001)。在吡格列酮组中,2年时低密度脂蛋白胆固醇均值与基线均值相似。

结论/解读:2年后,当吡格列酮添加到二甲双胍或磺脲类药物治疗中时,观察到甘油三酯显著降低且高密度脂蛋白胆固醇升高,且这种变化随时间持续甚至有所改善。吡格列酮对血脂的这些作用可能对降低2型糖尿病患者的心血管风险具有潜在益处。

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