Genetics of Type 2 Diabetes: Opportunities for Precision Medicine: JACC Focus Seminar.

Genetics of Type 2 Diabetes: Opportunities for Precision Medicine: JACC Focus Seminar.
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2型糖尿病的遗传学:精准医学的机会:JACC焦点研讨会。

DOI:
10.1016/j.jacc.2021.03.346
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发表时间:
2021-08-03
影响因子:
24
通讯作者:
Knowles JW
Knowles JW
中科院分区:
医学1区
文献类型:
--
作者:
Kim DS;Gloyn AL;Knowles JW

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2型糖尿病(T2D)非常普遍,是心血管疾病(CVD)的重要诱因。然而,在疾病发病机制和并发症风险方面存在显著的异质性。我们对与t2d风险相关的遗传变异和疾病相关数量性状变异进行编目的能力取得了巨大进展。这些发现有可能为安全有效的治疗开发提供可控制的靶点和途径,但精准医学的前景一直难以实现。最近的研究已经确定了具有中间表型(例如,脂质水平,空腹胰岛素,BMI)差异风险的个体亚组,这些亚组有助于解释观察到的临床异质性。这些“分区遗传风险评分”不仅有可能识别出心血管疾病风险最高和疾病进展迅速的患者,而且还可以帮助患者分层,弥合T2D精准医疗的差距。2型糖尿病(T2D)在发病机制和病程/并发症方面具有显著的异质性。最近的进展已经确定了T2D的亚组,有助于解释观察到的临床异质性。特别是,T2D亚群聚类的遗传方法有可能识别下游并发症(如心脏病)和疾病进展(如胰岛素需用T2D)风险更高的患者。遗传方法已经确定并验证了T2D的新药物靶点,也可能允许更有针对性的治疗方法。总之,聚类方法有可能将精准医学带入t2dm预防和治疗的临床。
Type 2 diabetes (T2D) is highly prevalent and a strong contributor for cardiovascular disease (CVD). However, there is significant heterogeneity in disease pathogenesis and the risk of complications. Enormous progress has been made in our ability to catalog genetic variation associated with T2D-risk and variation in disease relevant quantitative traits. These discoveries hold the potential to shed light on tractable targets and pathways for safe and effective therapeutic development, but the promise of precision medicine has been slow to be realized. Recent studies have identified subgroups of individuals with differential risk for intermediate phenotypes (e.g., lipid levels, fasting insulin, BMI), which contribute to T2D risk, helping to account for the observed clinical heterogeneity. These “partitioned genetic risk scores” have not only the potential to identify patients at greatest risk of CVD and rapid disease progression, but could also aid patient stratification bridging the gap towards precision medicine for T2D. Type 2 diabetes (T2D) has significant heterogeneity in its pathogenesis and disease course/complications. Recent advances have identified subgroups within T2D, helping to account for the clinical heterogeneity observed. In particular, genetic approaches to clustering subgroups of T2D have the potential to identify patients at greater risk of downstream complications (e.g., heart disease) and disease progression (e.g., insulin requiring T2D). Genetic approaches have identified and validated new drug targets for T2D and may also allow more targeted therapeutic approaches. Together, clustering methods have the potential to bring precision medicine into the clinic for T2D prevention and treatment.
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