Genome-Wide and Abdominal MRI Data Provide Evidence That a Genetically Determined Favorable Adiposity Phenotype Is Characterized by Lower Ectopic Liver Fat and Lower Risk of Type 2 Diabetes, Heart Disease, and Hypertension

内科学 内分泌学 等位基因 2型糖尿病 脂肪组织 糖尿病 医学 腹内脂肪 脂肪变性 生物 胰岛素抵抗 遗传学 基因 内脏脂肪
作者
Yingjie Ji,Andrianos M. Yiorkas,Francesca Frau,Dennis O. Mook‐Kanamori,Harald Staiger,E. Louise Thomas,Naeimeh Atabaki‐Pasdar,Archie Campbell,Jessica Tyrrell,Samuel E. Jones,Robin N. Beaumont,Andrew R. Wood,Marcus A. Tuke,Katherine S. Ruth,Anubha Mahajan,Anna Murray,Rachel M. Freathy,Michael N. Weedon,Andrew T. Hattersley,Caroline Hayward
出处
期刊:Diabetes [American Diabetes Association]
卷期号:68 (1): 207-219 被引量:94
标识
DOI:10.2337/db18-0708
摘要

Recent genetic studies have identified alleles associated with opposite effects on adiposity and risk of type 2 diabetes. We aimed to identify more of these variants and test the hypothesis that such favorable adiposity alleles are associated with higher subcutaneous fat and lower ectopic fat. We combined MRI data with genome-wide association studies of body fat percentage (%) and metabolic traits. We report 14 alleles, including 7 newly characterized alleles, associated with higher adiposity but a favorable metabolic profile. Consistent with previous studies, individuals carrying more favorable adiposity alleles had higher body fat % and higher BMI but lower risk of type 2 diabetes, heart disease, and hypertension. These individuals also had higher subcutaneous fat but lower liver fat and a lower visceral-to-subcutaneous adipose tissue ratio. Individual alleles associated with higher body fat % but lower liver fat and lower risk of type 2 diabetes included those in PPARG, GRB14, and IRS1, whereas the allele in ANKRD55 was paradoxically associated with higher visceral fat but lower risk of type 2 diabetes. Most identified favorable adiposity alleles are associated with higher subcutaneous and lower liver fat, a mechanism consistent with the beneficial effects of storing excess triglycerides in metabolically low-risk depots.
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