Khan M, Xu Y, Edwards G, Urquhart R, Mariz S
Takeda Pharmaceuticals North America Inc, Lincolnshire, IL, USA.
Int J Clin Pract. 2004 Oct;58(10):907-12. doi: 10.1111/j.1368-5031.2004.00258.x.
A total of 3,713 patients with poorly controlled type 2 diabetes were enroled into four multicentre, double-blind studies and randomised to receive pioglitazone, sulphonylurea, metformin or a combination of two of these agents for up to 52 weeks. Data from patients with a lipid evaluation, at week 52, were pooled, and treatment groups were compared using analysis of covariance. Pioglitazone, alone or combined with metformin or sulphonylurea, resulted in mean decreases in triglycerides (-9 to -11%), total/HDL cholesterol ratio (-9 to -10%) and free fatty acid (-0.051 to -0.123 mmol/l) and mean increases in HDL cholesterol (17 to 20%). The sustained, favourable effects of pioglitazone on important components of diabetic dyslipidaemia may contribute to reduced cardiovascular disease risk, among patients with type 2 diabetes.
共有3713例2型糖尿病控制不佳的患者被纳入四项多中心、双盲研究,并随机接受吡格列酮、磺脲类药物、二甲双胍或其中两种药物的联合治疗,为期52周。汇总了第52周进行血脂评估的患者数据,并使用协方差分析对治疗组进行比较。吡格列酮单独使用或与二甲双胍或磺脲类药物联合使用,可使甘油三酯平均降低(-9%至-11%)、总胆固醇/高密度脂蛋白胆固醇比值降低(-9%至-10%)、游离脂肪酸降低(-0.051至-0.123 mmol/l),高密度脂蛋白胆固醇平均升高(17%至20%)。吡格列酮对糖尿病血脂异常重要成分的持续、有利影响可能有助于降低2型糖尿病患者的心血管疾病风险。