孟德尔随机化
2型糖尿病
全基因组关联研究
疾病
2型糖尿病
冠心病
遗传关联
人口
医学
糖尿病
孟德尔遗传
心脏病
生物信息学
遗传学
生物
内科学
单核苷酸多态性
遗传变异
内分泌学
基因
基因型
环境卫生
作者
Mark O. Goodarzi,Jerome I. Rotter
出处
期刊:Circulation Research
[Lippincott Williams & Wilkins]
日期:2020-05-21
卷期号:126 (11): 1526-1548
被引量:98
标识
DOI:10.1161/circresaha.119.316065
摘要
Diabetes mellitus is a major risk factor for coronary heart disease (CHD). The major form of diabetes mellitus is type 2 diabetes mellitus (T2D), which is thus largely responsible for the CHD association in the general population. Recent years have seen major advances in the genetics of T2D, principally through ever-increasing large-scale genome-wide association studies. This article addresses the question of whether this expanding knowledge of the genomics of T2D provides insight into the etiologic relationship between T2D and CHD. We will investigate this relationship by reviewing the evidence for shared genetic loci between T2D and CHD; by examining the formal testing of this interaction (Mendelian randomization studies assessing whether T2D is causal for CHD); and then turn to the implications of this genetic relationship for therapies for CHD, for therapies for T2D, and for therapies that affect both. In conclusion, the growing knowledge of the genetic relationship between T2D and CHD is beginning to provide the promise for improved prevention and treatment of both disorders.
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