[Tirzepatide : overview of clinical studies SURPASS in type 2 diabetes and SURMOUNT in obesity].

Revue medicale de Liege Pub Date : 2024-12-01
André Scheen
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引用次数: 0

Abstract

Tirzepatide is a unimolecular dual agonist of both glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) receptors, which has been developed as once-weekly injection first for the treatment of type 2 diabetes (T2DM), then for the treatment of obesity. Because of the complementarity of action of the two incretins, tirzepatide showed, in a dose-dependent manner (5, 10 and 15 mg), a better efficacy (greater reduction in HbA1c and body weight) compared with placebo, semaglutide 1 mg, basal insulin and preprandial boluses of insulin lispro in six studies of the SURPASS programme. In the SURMOUNT programme, tirzepatide showed a marked reduction in body weight, never reached before with a drug, among people with obesity or overweight associated with complications linked to excess weight. Such weight loss was accompanied by an improvement of comorbidities (as sleep apnea syndrome) and cardiovascular risk factors. Two large cardiovascular outcome trials are ongoing in patients with T2DM (SURPASS-CVOT) and in patients with obesity (SURMOUNT-MMO).

[替西肽:2型糖尿病的transcend和肥胖症的SURMOUNT临床研究综述]。
tizepatide是胰高血糖素样肽-1 (GLP-1)和葡萄糖依赖性胰岛素性多肽(GIP)受体的单分子双激动剂,已被开发为每周一次注射,首先用于治疗2型糖尿病(T2DM),然后用于治疗肥胖。由于两种肠促胰岛素的互补性,在六项研究中,与安慰剂、西马鲁肽、基础胰岛素和餐前胰岛素利斯pro相比,替西帕肽以剂量依赖性的方式(5,10和15mg)显示出更好的疗效(更大程度地降低HbA1c和体重)。在SURMOUNT项目中,替西帕肽在肥胖或超重并伴有超重并发症的人群中显示出了体重的显著降低,这是以往任何药物都无法达到的。这种体重减轻伴随着合并症(如睡眠呼吸暂停综合征)和心血管危险因素的改善。2型糖尿病患者(SURPASS-CVOT)和肥胖患者(SURMOUNT-MMO)的两项大型心血管结局试验正在进行中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.60
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