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Genomic-based tools for the risk assessment management and prevention of type 2 diabetes

机译:基于基因组的工具用于2型糖尿病的风险评估管理和预防

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摘要

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.
机译:2型糖尿病(T2D)是一种常见且严重的疾病,是发展为心血管疾病,神经病,肾病,视网膜病,牙周病以及足溃疡和截肢的重要危险因素。与T2D相关的疾病负担导致人们着重于早期识别数百万高危人群,以便可以在疾病进展开始之前有效地实施管理和干预策略。随着对T2D遗传基础知识的了解越来越多,已经测试了几种基于基因组的策略改善风险评估,管理和预防的能力。已经开发了遗传风险评分,目的是更准确地识别那些有患T2D风险的人,并可能改善动机和对生活方式改变计划的坚持。此外,越来越多的证据表明,口服降血糖药物在许多患者中会发生药物基因组学变异,这表明基因组学可能很快会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,对个人的影响不同,因此风险预测和治疗对医疗保健提供者可能具有挑战性。基因组方法有望改善风险预测并为个别患者量身定制管理,并为患有T2D的患者带来更好的健康结果。

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