Miles John M, Leiter Lawrence, Hollander Priscilla, Wadden Thomas, Anderson James W, Doyle Michael, Foreyt John, Aronne Louis, Klein Samuel
Lipid and Diabetes Research Center, St. Lukes Hospital, Kansas City, Missouri, USA.
Diabetes Care. 2002 Jul;25(7):1123-8. doi: 10.2337/diacare.25.7.1123.
The purpose of this study was to assess the effect of orlistat, a gastrointestinal lipase inhibitor, on body weight, glycemic control, and cardiovascular risk factors in metformin-treated type 2 diabetic patients.
A 1-year multicenter, randomized, double-blind, placebo-controlled trial of 120 mg orlistat t.i.d. (n = 249) or placebo (n = 254) combined with a reduced-calorie diet was conducted in overweight and obese patients with suboptimal control of type 2 diabetes.
After 1 year of treatment, mean (+/-SE) weight loss was greater in the orlistat than in the placebo group (-4.6 +/- 0.3% vs. -1.7 +/- 0.3% of baseline wt, P < 0.001). Orlistat treatment caused a greater improvement in glycemic control than placebo, as evidenced by a greater reduction in serum HbA(1c), adjusted for changes in metformin and sulfonylurea therapy (-0.90 +/- 0.08 vs. -0.61 +/- 0.08, P = 0.014); a greater proportion of patients achieving decreases in HbA(1c) of > or = 0.5 and > or = 1.0% (both P < 0.01); and a greater reduction in fasting serum glucose (-2.0 +/- 0.2 vs. -0.7 +/- 0.2 mmol/l, P = 0.001). Compared with the placebo group, patients treated with orlistat also had greater decreases in total cholesterol, LDL cholesterol, and systolic blood pressure (all P < 0.05). Although more subjects treated with orlistat experienced gastrointestinal side effects than placebo (83 vs. 62%, P < 0.05), more subjects in the placebo group withdrew prematurely from the study than in the orlistat group (44 vs. 35%, P < 0.05).
Orlistat is a useful adjunctive treatment for producing weight loss and improving glycemic control, serum lipid levels, and blood pressure in obese patients with type 2 diabetes who are being treated with metformin.
本研究旨在评估胃肠道脂肪酶抑制剂奥利司他对接受二甲双胍治疗的2型糖尿病患者体重、血糖控制及心血管危险因素的影响。
在超重和肥胖且2型糖尿病控制不佳的患者中开展了一项为期1年的多中心、随机、双盲、安慰剂对照试验,试验内容为每日3次服用120 mg奥利司他(n = 249)或安慰剂(n = 254)并结合低热量饮食。
治疗1年后,奥利司他组的平均(±标准误)体重减轻幅度大于安慰剂组(较基线体重分别下降-4.6±0.3%和-1.7±0.3%,P<0.001)。奥利司他治疗比安慰剂能更好地改善血糖控制,这体现在血清糖化血红蛋白(HbA1c)降低幅度更大(校正二甲双胍和磺脲类药物治疗的变化后,-0.90±0.08比-0.61±0.08,P = 0.014);更多患者的HbA1c降低幅度≥0.5%和≥1.0%(均P<0.01);空腹血清葡萄糖降低幅度更大(-2.0±0.2比-0.7±0.2 mmol/L,P = 0.001)。与安慰剂组相比,接受奥利司他治疗的患者总胆固醇、低密度脂蛋白胆固醇和收缩压降低幅度也更大(均P<0.05)。虽然接受奥利司他治疗的受试者出现胃肠道副作用的比例高于安慰剂组(83%对62%,P<0.05),但安慰剂组中提前退出研究的受试者比例高于奥利司他组(44%对35%,P<0.05)。
对于正在接受二甲双胍治疗的肥胖2型糖尿病患者,奥利司他是一种有助于减轻体重、改善血糖控制、血脂水平和血压的辅助治疗药物。