Keating G M, Jarvis B
Adis International Limited, Auckland, New Zealand.
Drugs. 2001;61(14):2107-19; discussion 2120-1. doi: 10.2165/00003495-200161140-00011.
Orlistat is a nonsystemically acting gastric and pancreatic lipase inhibitor that limits the absorption of dietary fat. A retrospective pooled analysis of three 2-year, double-blind, randomised, placebo-controlled trials involving patients with obesity revealed that orlistat recipients were more likely to experience an improvement, and less likely to experience a deterioration, in glucose tolerance status than placebo recipients. In comparison with placebo, orlistat recipients had significantly greater reductions in glycosylated haemoglobin and fasting plasma glucose levels in large, double-blind, randomised, placebo-controlled studies of 24 to 52 weeks' duration involving patients with obesity and type 2 diabetes mellitus. In one such study, the dosage of concomitant sulphonylureas was able to be reduced in more orlistat than placebo recipients (43.2 vs 28.9%), with discontinuation of sulphonylurea therapy achieved in 11.7% of orlistat recipients. The most common adverse effects reported in orlistat recipients with type 2 diabetes mellitus relate to the gastrointestinal system and are similar to those reported in studies involving patients without type 2 diabetes mellitus.
奥利司他是一种非全身性作用的胃和胰脂肪酶抑制剂,可限制膳食脂肪的吸收。一项对三项为期2年的双盲、随机、安慰剂对照试验(涉及肥胖患者)的回顾性汇总分析显示,与安慰剂组相比,接受奥利司他治疗的患者糖耐量状态更有可能改善,恶化的可能性更小。在涉及肥胖和2型糖尿病患者的为期24至52周的大型双盲、随机、安慰剂对照研究中,与安慰剂相比,接受奥利司他治疗的患者糖化血红蛋白和空腹血糖水平显著降低。在一项此类研究中,与安慰剂组相比,更多接受奥利司他治疗的患者(43.2%对28.9%)能够减少磺脲类药物的用量,11.7%接受奥利司他治疗的患者停用了磺脲类药物治疗。在2型糖尿病患者中,接受奥利司他治疗的患者报告的最常见不良反应与胃肠道系统有关,与在不患有2型糖尿病患者的研究中报告的不良反应相似。