Blüher Matthias
Helmholtz-Institut für Metabolismus‑, Adipositas- und Gefäßforschung (HI-MAG), Helmholtz Zentrum München an der Universität Leipzig und dem Universitätsklinikum Leipzig AöR, Philipp-Rosenthal-Straße 27, 04103, Leipzig, Deutschland.
Klinik und Poliklinik für Endokrinologie, Nephrologie und Rheumatologie, Bereich Endokrinologie, Universität Leipzig, Leipzig, Deutschland.
Inn Med (Heidelb). 2025 May;66(5):475-484. doi: 10.1007/s00108-025-01897-2. Epub 2025 Apr 25.
Pharmacotherapy is part of a comprehensive guideline-conform treatment concept for people with obesity. The foundation of obesity treatment is initially a conservative multimodal basic treatment and consists of a low-energy diet, increased physical activity and behavioral changes. If the individual treatment goals are not achieved with this approach, medications can support the basic treatment. The concept is that drugs should not only achieve weight reduction and stabilization of the reduced body weight but also provide better long-term treatment for the chronic multisystem disease obesity. The incretin-based pharmacotherapy with liraglutide, semaglutide and tirzepatide, which have been introduced in recent years, have not only pronounced weight-reducing but also beneficial cardiometabolic effects. These include improvements in obesity-related comorbidities, such as type 2 diabetes, hypertension, fatty liver disease, obstructive sleep apnea, cardiovascular risk factors, chronic kidney disease and others. In contrast, incretin-based pharmacotherapy is typically associated with mild to moderate gastrointestinal side effects. With the marketing launch of setmelanotide, a medication became available for the treatment of rare monogenic forms of obesity. In addition, numerous incretin-based active agents and new substance classes are in advanced phases of clinical development. Due to their favorable efficacy and side effect profiles and also with respect to the positive cardiometabolic effects, the new drugs have the potential to significantly increase the importance of pharmacotherapy of obesity in Germany.
药物治疗是肥胖症患者综合循证治疗理念的一部分。肥胖症治疗的基础最初是保守的多模式基础治疗,包括低能量饮食、增加身体活动和行为改变。如果通过这种方法未实现个体治疗目标,药物可辅助基础治疗。其理念是,药物不仅应实现体重减轻和减轻后的体重稳定,还应为慢性多系统疾病肥胖症提供更好的长期治疗。近年来引入的基于肠促胰素的利拉鲁肽、司美格鲁肽和替尔泊肽药物治疗,不仅有显著的减重效果,还有有益的心脏代谢作用。这些作用包括改善与肥胖相关的合并症,如2型糖尿病、高血压、脂肪肝疾病、阻塞性睡眠呼吸暂停、心血管危险因素、慢性肾病等。相比之下,基于肠促胰素的药物治疗通常伴有轻度至中度胃肠道副作用。随着setmelanotide的上市,一种可用于治疗罕见单基因肥胖症的药物问世。此外,众多基于肠促胰素的活性剂和新物质类别正处于临床开发的后期阶段。鉴于其良好的疗效和副作用特征,以及积极的心脏代谢作用,这些新药有可能显著提升德国肥胖症药物治疗的重要性。