Hollander P A, Elbein S C, Hirsch I B, Kelley D, McGill J, Taylor T, Weiss S R, Crockett S E, Kaplan R A, Comstock J, Lucas C P, Lodewick P A, Canovatchel W, Chung J, Hauptman J
Baylor Medical Center, Dallas, Texas, USA.
Diabetes Care. 1998 Aug;21(8):1288-94. doi: 10.2337/diacare.21.8.1288.
Obesity is an important risk factor for type 2 diabetes. Weight loss in patients with type 2 diabetes is associated with improved glycemic control and reduced cardiovascular disease risk factors, but weight loss is notably difficult to achieve and sustain with caloric restriction and exercise. The purpose of this study was to assess the impact of treatment with orlistat, a pancreatic lipase inhibitor, on weight loss, glycemic control, and serum lipid levels in obese patients with type 2 diabetes on sulfonylurea medications.
In a multicenter 57-week randomized double-blind placebo-controlled study, 120 mg orlistat or placebo was administered orally three times a day with a mildly hypocaloric diet to 391 obese men and women with type 2 diabetes who were aged > 18 years, had a BMI of 28-40 kg/m2, and were clinically stable on oral sulfonylureas. Changes in body weight, glycemic control, lipid levels, and drug tolerability were measured.
After 1 year of treatment, the orlistat group lost 6.2 +/- 0.45% (mean +/- SEM) of initial body weight vs. 4.3 +/- 0.49% in the placebo group (P < 0.001). Twice as many patients receiving orlistat (49 vs. 23%) lost > or = 5% of initial body weight (P < 0.001). Orlistat treatment plus diet compared with placebo plus diet was associated with significant improvement in glycemic control, as reflected in decreases in HbA1c (P < 0.001) and fasting plasma glucose (P < 0.001) and in dosage reductions of oral sulfonylurea medication (P < 0.01). Orlistat therapy also resulted in significantly greater improvements than placebo in several lipid parameters, namely, greater reductions in total cholesterol, (P < 0.001), LDL cholesterol (P < 0.001), triglycerides (P < 0.05), apolipoprotein B (P < 0.001), and the LDL-to-HDL cholesterol ratio (P < 0.001). Mild to moderate and transient gastrointestinal events were reported with orlistat therapy, although their association with study withdrawal was low. Fat-soluble vitamin levels generally remained within the reference range, and vitamin supplementation was required in only a few patients.
Orlistat is an effective treatment modality in obese patients with type 2 diabetes with respect to clinically meaningful weight loss and maintenance of weight loss, improved glycemic control, and improved lipid profile.
肥胖是2型糖尿病的重要危险因素。2型糖尿病患者体重减轻与血糖控制改善及心血管疾病危险因素降低相关,但仅通过热量限制和运动很难实现并维持体重减轻。本研究旨在评估胰脂肪酶抑制剂奥利司他治疗对服用磺脲类药物的2型糖尿病肥胖患者体重减轻、血糖控制及血脂水平的影响。
在一项为期57周的多中心随机双盲安慰剂对照研究中,391名年龄大于18岁、BMI为28 - 40 kg/m²且口服磺脲类药物临床稳定的2型糖尿病肥胖男性和女性,每天口服三次120 mg奥利司他或安慰剂,并搭配轻度低热量饮食。测量体重、血糖控制、血脂水平及药物耐受性的变化。
治疗1年后,奥利司他组初始体重减轻了6.2±0.45%(均值±标准误),而安慰剂组为4.3±0.49%(P<0.001)。接受奥利司他治疗的患者中有两倍多(49%对23%)体重减轻≥初始体重的5%(P<0.001)。与安慰剂加饮食相比,奥利司他治疗加饮食与血糖控制的显著改善相关,表现为糖化血红蛋白(HbA1c)降低(P<0.001)、空腹血糖降低(P<0.001)以及口服磺脲类药物剂量减少(P<0.01)。奥利司他治疗在几个血脂参数方面也比安慰剂有更显著改善,即总胆固醇降低幅度更大(P<0.001)、低密度脂蛋白胆固醇(LDL胆固醇)降低幅度更大(P<0.001)、甘油三酯降低(P<0.05)、载脂蛋白B降低(P<0.001)以及LDL胆固醇与高密度脂蛋白胆固醇(HDL胆固醇)比值降低(P<0.001)。奥利司他治疗报告有轻度至中度短暂胃肠道事件,但其与退出研究的关联较低。脂溶性维生素水平一般保持在参考范围内,仅少数患者需要补充维生素。
对于有临床意义的体重减轻及维持体重减轻改善血糖控制和改善血脂谱而言,奥利司他是治疗2型糖尿病肥胖患者的有效治疗方式。