首页> 美国卫生研究院文献>BMJ Open >Treatment of antipsychotic-associated obesity with a GLP-1 receptor agonist—protocol for an investigator-initiated prospective randomised placebo-controlled double-blinded intervention study: the TAO study protocol
【2h】

Treatment of antipsychotic-associated obesity with a GLP-1 receptor agonist—protocol for an investigator-initiated prospective randomised placebo-controlled double-blinded intervention study: the TAO study protocol

机译:用GLP-1受体激动剂治疗抗精神病相关性肥胖症的方法-一项由研究者发起的前瞻性随机安慰剂对照双盲干预研究的协议:TAO研究方案

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

IntroductionAntipsychotic medication is widely associated with dysmetabolism including obesity and type 2 diabetes, cardiovascular-related diseases and early death. Obesity is considered the single most important risk factor for cardiovascular morbidity and mortality. Interventions against antipsychotic-associated obesity are limited and insufficient. Glucagon-like peptide-1 (GLP-1) receptor agonists are approved for the treatment of type 2 diabetes, but their bodyweight-lowering effects have also been recognised in patients with non-diabetes. The primary endpoint of this trial is weight loss after 3 months of treatment with a GLP-1 receptor agonist (exenatide once weekly) in patients with non-diabetic schizophrenia with antipsychotic-associated obesity. Secondary endpoints include physiological and metabolic measurements, various psychopathological and cognitive measures, and structural and functional brain MRI.
机译:引言抗精神病药物广泛地与代谢异常有关,包括肥胖和2型糖尿病,心血管相关疾病和早逝。肥胖被认为是心血管疾病发病率和死亡率的最重要的单一危险因素。与抗精神病药物相关的肥胖症的干预措施有限且不足。胰高血糖素样肽-1(GLP-1)受体激动剂已被批准用于治疗2型糖尿病,但在非糖尿病患者中也已认识到它们的降体重作用。该试验的主要终点是在患有抗精神病相关性肥胖的非糖尿病精神分裂症患者中,使用GLP-1受体激动剂(艾塞那肽,每周一次)治疗3个月后的体重减轻。次要终点包括生理和代谢测量,各种心理病理和认知测量以及脑部结构和功能MRI。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号