年轻成熟型糖尿病患者的新型治疗方案。

Karsten Müssig
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摘要

青年成熟期糖尿病(MODY)是最常见的单基因糖尿病,具有常染色体显性遗传模式。MODY是由于对胰岛β细胞的发育和功能有重要影响的基因发生突变,导致胰岛素分泌能力受损而引起的。迄今为止,已描述了 14 种不同的类型。GCK-MODY(原 MODY-2)一般不需要药物治疗,而其他类型的 MODY,如 HNF1A-MODY(原 MODY-3)和 HNF4A(原 MODY-1)通常对磺脲类药物治疗反应良好。然而,这些 MODY 病型的特点是病程呈进行性发展,这意味着随着病情的发展,通常需要使用胰岛素治疗。磺脲类药物治疗和胰岛素治疗都会增加低血糖和体重增加的风险。较新的降血糖疗法,如 SGLT2 抑制剂 (SGLT2i)、DPP-4 抑制剂 (DPP4i) 和 GLP-1 受体激动剂 (GLP-1RA),发生低血糖的风险要低得多,而且通常对体重有有利影响。本综述旨在根据以前发表的临床研究、系列病例和病例报告,概述用 SGLT2i、DPP4i 和 GLP-1RA 治疗 MODY 患者的情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel Treatment Options in Patients with Maturity-Onset Diabetes of the Young.

Maturity-onset diabetes of the young (MODY) is the most common monogenetic form of diabetes with an autosomal dominant inheritance pattern. MODY is caused by mutations in genes important for the development and function of pancreatic beta cells, resulting in impaired insulin secretion capacity. To date, 14 different types have been described. While glucokinase (GCK)-MODY (formerly MODY-2) generally requires no drug therapy, other forms of MODY, such as hepatocyte nuclear factor-1-alpha (HNF1A)-MODY (formerly MODY-3) and HNF4A (formerly MODY-1), usually respond very well to sulfonylurea therapy. However, these MODY forms are characterised by a progressive course, meaning that insulin therapy is often required as the disease progresses. Both sulfonylurea therapy and insulin therapy are associated with an increased risk of hypoglycaemia and frequent weight gain. Newer blood glucose-lowering therapies, such as SGLT2 inhibitors (SGLT2i), DPP-4 inhibitors (DPP4i) and GLP-1 receptor agonists (GLP-1RA), have a much lower risk of hypoglycaemia and usually have a favourable effect on body weight. This review aims to provide an overview of the treatment of MODY patients with SGLT2i, DPP4i and GLP-1RA on the basis of previously published clinical studies, case series and case reports.

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