Insights into the Genetic Underpinnings of Endocrine Traits from Large-Scale Genome-Wide Association Studies

被引:1
|
作者
Cousminer, Diana L. [1 ,2 ]
Grant, Struan F. A. [1 ,2 ]
机构
[1] Childrens Hosp Philadelphia, Ctr Spatial & Funct Genom, Dept Pediat, Div Human Genet, 3615 Civ Ctr Blvd, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Dept Genet, Clin Res Bldg 500,415 Curie Blvd, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
Genome-wide association studies; BMI; Height; Puberty; Diabetes; Bone density; Endocrine traits; BONE-DENSITY; RISK SCORE; TYPE-1; VARIANTS; FTO; CHILDHOOD; BIRTH; LOCI; LIFE; DISCRIMINATION;
D O I
10.1016/j.ecl.2020.07.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Great strides have been made in genetic association studies of endocrine traits and diseases, with hundreds or thousands of variants associated with height, body mass index, bone density, pubertal timing, and diabetes in recent years. The common variants associated with these traits explain up to half of the trait variation owing to genetic factors, and when aggregated into polygenic risk scores, can also impact clinically relevant phenotypes at the tail ends of the trait distributions. However, pediatric studies tend to lag behind, and it is often unclear how adult-associated variants behave across life.
引用
收藏
页码:725 / +
页数:16
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