Johansen Taber Katherine A, Dickinson Barry D
Department of Science and Biotechnology, American Medical Association, Chicago, IL, USA.
Appl Clin Genet. 2015 Jan 7;8:1-8. doi: 10.2147/TACG.S75583. eCollection 2015.
Type 2 diabetes (T2D) is a common and serious disorder and is a significant risk factor for the development of cardiovascular disease, neuropathy, nephropathy, retinopathy, periodontal disease, and foot ulcers and amputations. The burden of disease associated with T2D has led to an emphasis on early identification of the millions of individuals at high risk so that management and intervention strategies can be effectively implemented before disease progression begins. With increasing knowledge about the genetic basis of T2D, several genomic-based strategies have been tested for their ability to improve risk assessment, management and prevention. Genetic risk scores have been developed with the intent to more accurately identify those at risk for T2D and to potentially improve motivation and adherence to lifestyle modification programs. In addition, evidence is building that oral antihyperglycemic medications are subject to pharmacogenomic variation in a substantial number of patients, suggesting genomics may soon play a role in determining the most effective therapies. T2D is a complex disease that affects individuals differently, and risk prediction and treatment may be challenging for health care providers. Genomic approaches hold promise for their potential to improve risk prediction and tailor management for individual patients and to contribute to better health outcomes for those with T2D.
2型糖尿病(T2D)是一种常见且严重的疾病,是心血管疾病、神经病变、肾病、视网膜病变、牙周疾病以及足部溃疡和截肢发生的重要风险因素。与T2D相关的疾病负担促使人们重视对数以百万计的高危个体进行早期识别,以便在疾病进展开始前有效实施管理和干预策略。随着对T2D遗传基础认识的不断增加,已经对几种基于基因组的策略进行了测试,以评估其改善风险评估、管理和预防的能力。已经开发了遗传风险评分,旨在更准确地识别T2D高危人群,并有可能提高对生活方式改变计划的积极性和依从性。此外,越来越多的证据表明,大量患者的口服降糖药物存在药物基因组学变异,这表明基因组学可能很快在确定最有效的治疗方法中发挥作用。T2D是一种复杂的疾病,对个体的影响各不相同,对医疗保健提供者来说,风险预测和治疗可能具有挑战性。基因组方法有望改善风险预测,为个体患者量身定制管理方案,并为T2D患者带来更好的健康结果。