The genetics of human obesity

被引:113
|
作者
Xia, Qianghua [1 ]
Grant, Struan F. A. [1 ,2 ,3 ]
机构
[1] Childrens Hosp Philadelphia, Res Inst, Div Human Genet, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Res Inst, Ctr Appl Gen, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA
来源
YEAR IN DIABETES AND OBESITY | 2013年 / 1281卷
关键词
obesity; genetics; monogenic; GWAS; human; BODY-MASS INDEX; GENOME-WIDE ASSOCIATION; BARDET-BIEDL-SYNDROME; LEPTIN RECEPTOR GENE; EARLY-ONSET OBESITY; FTO GENE; CHILDHOOD OBESITY; COMMON VARIANTS; MISSING HERITABILITY; ADIPONECTIN GENE;
D O I
10.1111/nyas.12020
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It has long been known that there is a genetic component to obesity, and that characterizing this underlying factor would likely offer the possibility of better intervention in the future. Monogenic obesity has proved to be relatively straightforward, with a combination of linkage analysis and mouse models facilitating the identification of multiple genes. In contrast, genome-wide association studies have successfully revealed a variety of genetic loci associated with the more common form of obesity, allowing for very strong consensus on the underlying genetic architecture of the phenotype for the first time. Although a number of significant findings have been made, it appears that very little of the apparent heritability of body mass index has actually been explained to date. New approaches for data analyses and advances in technology will be required to uncover the elusive missing heritability, and to aid in the identification of the key causative genetic underpinnings of obesity.
引用
收藏
页码:178 / 190
页数:13
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