Chua Marvin Wei Jie
Endocrinology Service, Department of General Medicine, Sengkang General Hospital, 110 Sengkang East Way, Singapore 544886, Singapore.
Clin Pract. 2021 Dec 21;12(1):1-7. doi: 10.3390/clinpract12010001.
Sodium-glucose co-transporter-2 (SGLT2) inhibitors and glucagon-like peptide 1 (GLP-1) agonists are important drugs in our armamentarium of treatment for Type 2 diabetes mellitus (DM). In addition to their glucose-lowering effects, they have effects on weight, other metabolic diseases and perhaps most importantly, a cardioprotective and reno-protective effect. Liraglutide is a long-acting GLP-1 agonist which was originally used at 1.8 mg daily for the treatment of DM. However, high-dose liraglutide-liraglutide 3 mg daily, has been demonstrated to be a safe and effective treatment for obesity, with or without DM. In this manuscript, I present two patients who had unusual responses to combination therapy with high-dose liraglutide and SGLT2 inhibitor-marked and/or rapid improvement in glycemic control and weight loss. Drawing from the observations in both cases, I discuss the complementary mechanisms of actions of both drugs, review the clinical effects of combination therapy and distil them into clinical pearls of practical utility for the physician. Given the "clash of the two pandemics" of obesity and COVID-19 and the burgeoning rates of obesity which loom in the near horizon, this is most timely.
钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂和胰高血糖素样肽1(GLP-1)激动剂是我们治疗2型糖尿病(DM)的重要药物。除了具有降血糖作用外,它们还对体重、其他代谢性疾病有影响,也许最重要的是,具有心脏保护和肾脏保护作用。利拉鲁肽是一种长效GLP-1激动剂,最初用于每日1.8毫克治疗DM。然而,高剂量利拉鲁肽——每日3毫克利拉鲁肽,已被证明是一种治疗肥胖症的安全有效方法,无论是否患有DM。在本手稿中,我介绍了两名患者,他们对高剂量利拉鲁肽和SGLT2抑制剂联合治疗有不同寻常的反应——血糖控制和体重减轻显著改善和/或迅速改善。从这两个病例的观察结果出发,我讨论了两种药物的互补作用机制,回顾了联合治疗的临床效果,并将其提炼为对医生具有实际应用价值的临床要点。鉴于肥胖症和2019冠状病毒病这“两种大流行的冲突”以及近期肥胖率的迅速上升,这是非常及时的。