Stein Stephanie A, Maloney Kristin L, Pollin Toni I
Department of Medicine, Division of Endocrinology, Diabetes & Nutrition, University of Maryland School of Medicine, Baltimore, Maryland.
Department of Medicine, Division of Endocrinology, Diabetes & Nutrition, University of Maryland School of Medicine, Baltimore, Maryland ; Program in Genetics and Genomic Medicine, University of Maryland School of Medicine, Baltimore, Maryland.
Curr Genet Med Rep. 2014 Jun 1;2(2):56-67. doi: 10.1007/s40142-014-0039-5.
Most diabetes is polygenic in etiology, with (type 1 diabetes, T1DM) or without (type 2 diabetes, T2DM) an autoimmune basis. Genetic counseling for diabetes generally focuses on providing empiric risk information based on family history and/or the effects of maternal hyperglycemia on pregnancy outcome. An estimated one to five percent of diabetes is monogenic in nature, e.g., maturity onset diabetes of the young (MODY), with molecular testing and etiology-based treatment available. However, recent studies show that most monogenic diabetes is misdiagnosed as T1DM or T2DM. While efforts are underway to increase the rate of diagnosis in the diabetes clinic, genetic counselors and clinical geneticists are in a prime position to identify monogenic cases through targeted questions during a family history combined with working in conjunction with diabetes professionals to diagnose and assure proper treatment and familial risk assessment for individuals with monogenic diabetes.
大多数糖尿病在病因上是多基因的,有(1型糖尿病,T1DM)或没有(2型糖尿病,T2DM)自身免疫基础。糖尿病的遗传咨询通常侧重于根据家族史和/或母亲高血糖对妊娠结局的影响提供经验性风险信息。估计有1%至5%的糖尿病本质上是单基因的,例如青年发病的成年型糖尿病(MODY),可进行分子检测并基于病因进行治疗。然而,最近的研究表明,大多数单基因糖尿病被误诊为T1DM或T2DM。虽然目前正在努力提高糖尿病诊所的诊断率,但遗传咨询师和临床遗传学家处于有利地位,可通过在家族史询问中提出针对性问题,结合与糖尿病专业人员合作,来识别单基因病例,从而为单基因糖尿病患者进行诊断、确保适当治疗以及进行家族风险评估。