{"title":"Personalized Medicine: Monogenic Diabetes.","authors":"Peter A Goulden, Jaime Vengoechea, Kent McKelvey","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Personalized medicine in diabetes is a topic which has gained significant momentum in recent years (Raz et al. 2013). A rapid rise in the number and combinations of diabetes therapies coupled with an unprecedented rise in diabetes prevalence rates has necessitated diabetes guidelines which emphasize the need for personalized patient-centered care (ADA 2014). There are many questions regarding the role genetics may be able to play in guiding therapy. Recent pharmacogenetic research has revealed polymorphisms that may impact patient response to metformin (Dong et al 2011) and glucagon-like-polypeptide-1 therapies (Smushkin et al. 2012). This may hold promise for helping identify patients who will better respond to specific agents and in the longer-term may help ensure a smooth journey along the therapeutic pathway. Monogenic or \"single-gene\" diabetes comprises nearly 2% of all cases of type 2 diabetes and provides a model for individualizing care. This review will discuss the diagnosis and treatment of this condition.</p>","PeriodicalId":75122,"journal":{"name":"The Journal of the Arkansas Medical Society","volume":"112 5","pages":"58-9"},"PeriodicalIF":0.0000,"publicationDate":"2015-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of the Arkansas Medical Society","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Personalized medicine in diabetes is a topic which has gained significant momentum in recent years (Raz et al. 2013). A rapid rise in the number and combinations of diabetes therapies coupled with an unprecedented rise in diabetes prevalence rates has necessitated diabetes guidelines which emphasize the need for personalized patient-centered care (ADA 2014). There are many questions regarding the role genetics may be able to play in guiding therapy. Recent pharmacogenetic research has revealed polymorphisms that may impact patient response to metformin (Dong et al 2011) and glucagon-like-polypeptide-1 therapies (Smushkin et al. 2012). This may hold promise for helping identify patients who will better respond to specific agents and in the longer-term may help ensure a smooth journey along the therapeutic pathway. Monogenic or "single-gene" diabetes comprises nearly 2% of all cases of type 2 diabetes and provides a model for individualizing care. This review will discuss the diagnosis and treatment of this condition.
糖尿病个体化医疗是近年来获得显著发展势头的一个话题(Raz et al. 2013)。糖尿病治疗方法的数量和组合的迅速增加,加上糖尿病患病率的空前上升,有必要制定糖尿病指南,强调个性化的以患者为中心的护理的必要性(ADA 2014)。关于遗传学在指导治疗中可能发挥的作用,有许多问题。最近的药物遗传学研究揭示了可能影响患者对二甲双胍反应的多态性(Dong et al. 2011)和胰高血糖素样多肽-1治疗(Smushkin et al. 2012)。这可能有助于确定对特定药物有更好反应的患者,从长远来看,可能有助于确保治疗途径的顺利进行。单基因或“单基因”糖尿病占所有2型糖尿病病例的近2%,并为个性化护理提供了一种模式。本文将讨论该病的诊断和治疗。