Laver Thomas W, Patel Kashyap A
Department of Clinical and Biomedical Science, University of Exeter, Exeter EX2 5DW, United Kingdom.
Eur J Endocrinol. 2025 Aug 29;193(3):R25-R29. doi: 10.1093/ejendo/lvaf172.
Maturity onset diabetes of the young (MODY) is the most common form of monogenic diabetes. A genetic diagnosis can help tailor treatment. However, it is vital to test the right genes. This review discusses the need to test the correct genes and widen the genes that are included on panels while also discussing examples of genes that should be removed from panels due to insufficient evidence. This is important to ensure the maximum number of patients receive a genetic diagnosis while avoiding misdiagnosis and mistreatment. To maximize the cost-benefit of genetic testing, we need to select the right patients for genetic testing-this review discusses criteria that increase the chance of a patient having a monogenic cause of their diabetes. Reduced penetrance, where some individuals have the pathogenic genotype but do not exhibit the phenotype, is now known to be increasingly common in MODY and other monogenic disorders. This has important implications when a variant is identified in an unaffected individual. This review highlights recent work that polygenic risk may play a role in determining penetrance.
青年发病的成年型糖尿病(MODY)是单基因糖尿病最常见的形式。基因诊断有助于定制治疗方案。然而,检测正确的基因至关重要。本综述讨论了检测正确基因的必要性以及扩大基因检测 panel 所包含基因的范围,同时还讨论了由于证据不足而应从 panel 中剔除的基因实例。这对于确保最大数量的患者获得基因诊断,同时避免误诊和误治非常重要。为了使基因检测的成本效益最大化,我们需要选择合适的患者进行基因检测——本综述讨论了增加患者患单基因糖尿病可能性的标准。现在已知在 MODY 和其他单基因疾病中,一些个体具有致病基因型但不表现出表型的外显率降低现象越来越普遍。当在未受影响的个体中鉴定出变异时,这具有重要意义。本综述强调了近期的研究工作,即多基因风险可能在决定外显率方面发挥作用。