Corcept Therapeutics Incorporated, Menlo Park, California, USA.
Obesity (Silver Spring). 2010 Dec;18(12):2295-300. doi: 10.1038/oby.2010.51. Epub 2010 Mar 25.
Antipsychotic medications are associated with significant weight gain, type 2 diabetes mellitus, dyslipidemia, and increased cardiovascular risk. The objective of this study was to determine whether mifepristone, a glucocorticoid receptor antagonist, could prevent risperidone-induced weight gain. Using a 2:2:1 randomization scheme, 76 lean, healthy men (BMI 18-23 kg/m(2)) age 18-40 years were randomized to risperidone (n = 30), risperidone plus mifepristone (n = 30) or mifepristone (n = 16) daily for 28 days in an institutional setting. Subjects were provided food ad libitum. Body weight was measured daily. Metabolic measures were taken at study onset, midpoint, and end. Analyses of covariance indicated that the group receiving risperidone plus placebo gained significantly more weight (P < 0.001) and exhibited a significantly greater increase in waist circumference (P < 0.05) than the group receiving risperidone plus mifepristone. Significant differences were also observed for metabolic measures including fasting insulin (P < 0.001) and triglyceride levels (P < 0.05). Mifepristone attenuated increases in weight and reduced the metabolic changes induced by risperidone use, replicating results from a prior study of olanzapine-induced weight gain. These findings suggest mechanistic involvement of the hypothalamic-pituitary-adrenal axis in the weight and cardiometabolic side effects of antipsychotic medications. Future research should continue to test the potential of glucocorticoid antagonists to alleviate the deleterious side effects associated with use of antipsychotic medications.
抗精神病药物会导致显著的体重增加、2 型糖尿病、血脂异常和心血管风险增加。本研究的目的是确定米非司酮(一种糖皮质激素受体拮抗剂)是否可以预防利培酮引起的体重增加。采用 2:2:1 随机分组方案,将 76 名健康、消瘦的男性(BMI 18-23kg/m2),年龄 18-40 岁,随机分为利培酮组(n = 30)、利培酮加米非司酮组(n = 30)或米非司酮组(n = 16),每日服用 28 天,在机构环境中。为受试者提供自由进食。每日测量体重。在研究开始、中点和结束时测量代谢指标。协方差分析表明,接受利培酮加安慰剂的组体重增加明显更多(P <0.001),腰围增加明显更大(P <0.05),而接受利培酮加米非司酮的组。代谢指标也存在显著差异,包括空腹胰岛素(P <0.001)和甘油三酯水平(P <0.05)。米非司酮减轻了体重增加,并减少了利培酮使用引起的代谢变化,复制了先前奥氮平引起的体重增加研究的结果。这些发现表明,下丘脑-垂体-肾上腺轴在抗精神病药物的体重和心血管代谢副作用中起作用。未来的研究应继续测试糖皮质激素拮抗剂减轻与使用抗精神病药物相关的有害副作用的潜力。