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首页> 外文期刊>Journal of Clinical Medicine >Current Progress in Pharmacogenetics of Second-Line Antidiabetic Medications: Towards Precision Medicine for Type 2 Diabetes
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Current Progress in Pharmacogenetics of Second-Line Antidiabetic Medications: Towards Precision Medicine for Type 2 Diabetes

机译:二线抗糖尿病药物药理学的最新进展:面向2型糖尿病的精准医学

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Precision medicine is a scientific and medical practice for personalized therapy based on patients’ individual genetic, environmental, and lifestyle characteristics. Pharmacogenetics and pharmacogenomics are also rapidly developing and expanding as a key element of precision medicine, in which the association between individual genetic variabilities and drug disposition and therapeutic responses are investigated. Type 2 diabetes (T2D) is a chronic metabolic disorder characterized by hyperglycemia mainly associated with insulin resistance, with the risk of clinically important cardiovascular, neurological, and renal complications. The latest consensus report from the American Diabetes Association and European Association for the Study of Diabetes (ADA-EASD) on the management of T2D recommends preferential use of glucagon-like peptide-1 (GLP-1) receptor agonists, sodium-glucose cotransporter-2 (SGLT2) inhibitors, and some dipeptidyl peptidase-4 (DPP-4) inhibitors after initial metformin monotherapy for diabetic patients with established atherosclerotic cardiovascular or chronic kidney disease, and with risk of hypoglycemia or body weight-related problems. In this review article, we summarized current progress on pharmacogenetics of newer second-line antidiabetic medications in clinical practices and discussed their therapeutic implications for precision medicine in T2D management. Several biomarkers associated with drug responses have been identified from extensive clinical pharmacogenetic studies, and functional variations in these genes have been shown to significantly affect drug-related glycemic control, adverse reactions, and risk of diabetic complications. More comprehensive pharmacogenetic research in various clinical settings will clarify the therapeutic implications of these genes, which may be useful tools for precision medicine in the treatment and prevention of T2D and its complications.
机译:精准医学是根据患者的个体遗传,环境和生活方式特征进行个性化治疗的科学和医学实践。药物遗传学和药物基因组学也正在迅速发展和扩展,作为精密医学的关键要素,其中研究了个体遗传变异性与药物配置和治疗反应之间的关系。 2型糖尿病(T2D)是一种慢性代谢性疾病,其特征是高血糖症,主要与胰岛素抵抗有关,具有临床上重要的心血管,神经和肾脏并发症的风险。美国糖尿病协会和欧洲糖尿病研究协会(ADA-EASD)关于T2D管理的最新共识报告建议优先使用胰高血糖素样肽1(GLP-1)受体激动剂,钠-葡萄糖共转运蛋白-在患有二甲双胍单一疗法的糖尿病患者中,已确定的2种(SGLT2)抑制剂和一些二肽基肽酶4(DPP-4)抑制剂在已确定的动脉粥样硬化性心血管疾病或慢性肾脏疾病且存在低血糖或体重相关问题风险的糖尿病患者中使用。在这篇综述文章中,我们总结了新型二线抗糖尿病药物在临床实践中的药物遗传学进展,并讨论了它们在T2D管理中对精准医学的治疗意义。从广泛的临床药物遗传学研究中已经鉴定出几种与药物反应相关的生物标记物,并且这些基因的功能变异已显示出显着影响与药物相关的血糖控制,不良反应和糖尿病并发症的风险。在各种临床环境中进行更全面的药物遗传学研究将阐明这些基因的治疗意义,这对于精密医学治疗和预防T2D及其并发症可能是有用的工具。

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