Seno Yohei, Ikeguchi Eri, Yabe Daisuke
Department of Diabetes, Endocrinology and Nutrition, Kyoto University Graduate School of Medicine, 54 Shogoin-kawahara-cho, Sakyo-ku, Kyoto, 606-8507 Japan.
Diabetol Int. 2025 May 15;16(3):457-468. doi: 10.1007/s13340-025-00818-w. eCollection 2025 Jul.
The management of type 2 diabetes has evolved significantly with the advent of incretin-based therapies, particularly dipeptidyl peptidase-4 inhibitors and glucagon-like peptide-1 receptor agonists. In Japan, where over 70% of individuals with diabetes are aged 65 or older and often exhibit a non-obese phenotype with impaired insulin secretion, dipeptidyl peptidase-4 inhibitors remain a cornerstone therapy due to their ability to enhance insulin secretion without increasing hypoglycemia risk. Meanwhile, in younger adults with obesity, glucagon-like peptide-1 receptor agonists play a crucial role by improving glycaemia, promoting weight loss, and offering cardiovascular and renal protection. A major breakthrough in 2023 was the introduction of glucose-dependent insulinotropic polypeptide/glucagon-like peptide-1 receptor agonist tirzepatide, which activates both receptors and has shown superior glucose-lowering and weight-reducing effects in both clinical trials and real-world Japanese settings. However, incretin-based therapies are frequently associated with gastrointestinal side effects, and concerns remain regarding their potential impact on pancreatic and biliary diseases as well as frailty and sarcopenia in older adults. In addition, inappropriate discontinuation of insulin following incretin therapy initiation has led to severe outcomes, emphasizing the need for careful clinical decision-making beyond trial data. Emerging incretin-related therapies are under investigation for obesity and metabolic disorders including type 2 diabetes. While these agents hold promise for enhanced metabolic, weight, and cardiorenal benefits, their long-term safety and applicability require further study. To optimize therapeutic strategies, adherence to evidence-based guidelines, such as the "Recommendations for the Safe Use of Incretin-Related Agents, Second Edition" by the Japanese Diabetes Society, is essential.
随着基于肠促胰岛素的疗法的出现,2型糖尿病的管理发生了显著变化,尤其是二肽基肽酶-4抑制剂和胰高血糖素样肽-1受体激动剂。在日本,超过70%的糖尿病患者年龄在65岁及以上,且通常表现为非肥胖型表型,伴有胰岛素分泌受损,由于二肽基肽酶-4抑制剂能够在不增加低血糖风险的情况下增强胰岛素分泌,因此仍然是基石疗法。与此同时,在肥胖的年轻成年人中,胰高血糖素样肽-1受体激动剂通过改善血糖、促进体重减轻以及提供心血管和肾脏保护发挥着关键作用。2023年的一项重大突破是引入了葡萄糖依赖性促胰岛素多肽/胰高血糖素样肽-1受体激动剂替尔泊肽,它能激活这两种受体,并且在临床试验和日本的实际应用中均显示出卓越的降糖和减重效果。然而基于肠促胰岛素的疗法常常伴有胃肠道副作用,并且对于它们对胰腺和胆道疾病以及老年人的虚弱和肌肉减少症的潜在影响仍然存在担忧。此外,在开始肠促胰岛素治疗后不适当停用胰岛素已导致严重后果,这强调了除试验数据外还需要谨慎进行临床决策。正在对包括2型糖尿病在内的肥胖和代谢紊乱的新兴肠促胰岛素相关疗法进行研究。虽然这些药物有望带来更大的代谢、体重以及心脏和肾脏方面的益处,但其长期安全性和适用性仍需进一步研究。为了优化治疗策略,遵循循证指南,如日本糖尿病学会的《肠促胰岛素相关药物安全使用建议(第二版)》至关重要。