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UGDP争议:34年的争议性模糊尘埃落定。

The UGDP controversy: thirty-four years of contentious ambiguity laid to rest.

作者信息

Schwartz Theodore B, Meinert Curtis L

机构信息

Department of Medicine, Rush University Medical Center, USA.

出版信息

Perspect Biol Med. 2004 Autumn;47(4):564-74. doi: 10.1353/pbm.2004.0071.

Abstract

The University Group Diabetes Program (UGDP), launched in 1960, was an early placebo-controlled, multi-center clinical trial devised to determine which, if any, of the treatments for type 2 diabetes was efficacious. Because of an excess of cardiac deaths in patients treated with tolbutamide, a sulfonylurea drug, investigators terminated this limb of the study. This decision was met with strong resistance from the parent drug company and many in the medical community. Subsequent clinical studies both supported and conflicted with the UDGP findings, so that the controversy has persisted. A rationale for sulfonylurea-induced cardiotoxicity emerged with the observation that these drugs block ischemic preconditioning, a protective maneuver that reduces myocardial damage after temporary blockage of coronary blood flow; this action of sulfonylureas provided laboratory support for the UGDP findings. The development of newer sulfonylurea drugs that do not block ischemic preconditioning has rendered the UGDP controversy moot and has preserved a place for sulfonylureas in the treatment of type 2 diabetes.

摘要

大学组糖尿病项目(UGDP)于1960年启动,是一项早期的安慰剂对照多中心临床试验,旨在确定2型糖尿病的治疗方法中,哪些(如果有的话)是有效的。由于使用甲苯磺丁脲(一种磺脲类药物)治疗的患者心脏死亡人数过多,研究人员终止了该研究的这一部分。这一决定遭到了母制药公司和许多医学界人士的强烈抵制。随后的临床研究既支持了UGDP的研究结果,也与之相矛盾,因此争议一直存在。随着观察到这些药物会阻断缺血预处理(一种在冠状动脉血流暂时阻断后减少心肌损伤的保护性机制),磺脲类药物导致心脏毒性的一个理论依据出现了;磺脲类药物的这一作用为UGDP的研究结果提供了实验室支持。新型磺脲类药物的开发不再阻断缺血预处理,使得UGDP的争议不再有实际意义,并为磺脲类药物在2型糖尿病治疗中保留了一席之地。

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