Luo Lin, Zhu Changsen, Yang Shaona, Sun Yuan, Rong Muyang, Li Tianrong
Department of Geriatrics, Kunming University of Science and Technology, The First People's Hospital of Yunnan Province, Kunming, China.
Department of Otolaryngology, Kunming University of Science and Technology, The First People's Hospital of Yunnan Province, Kunming, China.
Front Neurol. 2025 Sep 11;16:1640563. doi: 10.3389/fneur.2025.1640563. eCollection 2025.
Myotonic Dystrophy (DM) is a hereditary muscle disorder characterized by progressive muscle weakness, myotonia, and multi-system dysfunction. Based on clinical and genetic features, DM can be classified into Type 1 (Type 1 Myotonic Dystrophy, DM1) and Type 2 (Type 2 Myotonic Dystrophy, DM2), with DM1 being the most common subtype in adulthood. Diabetes, a metabolic disease, is defined by persistent hyperglycemia, typically resulting from insufficient insulin secretion or impaired insulin action. Among the various forms of diabetes, Type 2 Diabetes (T2DM) has the highest prevalence, accounting for approximately 90% of all cases. Research has shown that individuals with Myotonic Dystrophy Type 1 (DM1) often experience comorbid Type 2 Diabetes (T2DM), a phenomenon that not only significantly increases the clinical burden but is also closely associated with poor prognosis, severely impacting patients' quality of life. This review provides a comprehensive analysis of the latest research on insulin resistance in DM1 patients, shedding light on the underlying mechanisms of DM1-related T2DM. Additionally, it explores the common comorbidities shared by DM1 and T2DM, including those affecting the muscular, respiratory, cardiovascular, endocrine, and nervous systems, as well as cancer and depression. Finally, this article summarizes the most recent therapeutic strategies for managing DM1 with T2DM, focusing on glucose-lowering medications combined with emerging targeted therapies that address the core pathophysiology of DM1, showing promising preclinical outcomes. This review aims to provide a theoretical foundation for future research and clinical practice in the management of DM1 complicated by T2DM.
强直性肌营养不良(DM)是一种遗传性肌肉疾病,其特征为进行性肌肉无力、肌强直和多系统功能障碍。根据临床和遗传特征,DM可分为1型(1型强直性肌营养不良,DM1)和2型(2型强直性肌营养不良,DM2),DM1是成人中最常见的亚型。糖尿病是一种代谢性疾病,其定义为持续性高血糖,通常由胰岛素分泌不足或胰岛素作用受损引起。在各种糖尿病类型中,2型糖尿病(T2DM)的患病率最高,约占所有病例的90%。研究表明,1型强直性肌营养不良(DM1)患者常合并2型糖尿病(T2DM),这种现象不仅显著增加了临床负担,还与预后不良密切相关,严重影响患者的生活质量。本综述对DM1患者胰岛素抵抗的最新研究进行了全面分析,揭示了DM1相关T2DM的潜在机制。此外,还探讨了DM1和T2DM共有的常见合并症,包括影响肌肉、呼吸、心血管、内分泌和神经系统的合并症,以及癌症和抑郁症。最后,本文总结了治疗DM1合并T2DM的最新治疗策略,重点是降糖药物与针对DM1核心病理生理学的新兴靶向治疗相结合,显示出有前景的临床前结果。本综述旨在为未来研究和临床治疗DM1合并T2DM提供理论基础。