Susceptibility Variants for Waist Size in Relation to Abdominal, Visceral, and Hepatic Adiposity in Postmenopausal Women

被引:10
|
作者
Lim, Unhee [1 ]
Ernst, Thomas [4 ]
Wilkens, Lynne R. [1 ]
Albright, Cheryl L. [2 ,3 ]
Lum-Jones, Annette [1 ]
Seifried, Ann [1 ]
Buchthal, Steven D. [4 ]
Novotny, Rachel [1 ]
Kolonel, Laurence N. [1 ]
Chang, Linda [4 ]
Cheng, Iona [1 ]
Le Marchand, Loic [1 ]
机构
[1] Univ Hawaii, Program Epidemiol, Ctr Canc, Honolulu, HI 96813 USA
[2] Univ Hawaii, Sch Nursing & Dent Hyg, Ctr Canc, Honolulu, HI 96813 USA
[3] Univ Hawaii, Canc Prevent & Control Program, Ctr Canc, Honolulu, HI 96813 USA
[4] Univ Hawaii, John A Burns Sch Med, Honolulu, HI 96813 USA
基金
美国国家卫生研究院;
关键词
Body composition; Single nucleotide polymorphisms; Liver fat; Subcutaneous adipose tissue; Visceral adipose tissue; BODY-MASS INDEX; REGIONAL FAT DISTRIBUTION; FTO GENE; METABOLIC SYNDROME; LEPTIN RECEPTOR; CANCER-RISK; CARDIOVASCULAR RISK; MULTIETHNIC COHORT; LIFE-STYLE; LIVER FAT;
D O I
10.1016/j.jand.2012.03.034
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Genome-wide association studies have identified common genetic variants that can contribute specifically to the risk of abdominal adiposity, as measured by waist circumference or waist-to-hip ratio. However, it is unknown whether these genetic risk factors affect relative body fat distribution in the abdominal visceral and subcutaneous compartments. The association between imaging-based abdominal fat mass and waist-size risk variants in the FTO, LEPR, LYPLAL1, MSRA, NRXN3, and TFAP2B genes was investigated. A cross-sectional sample of 60 women was selected among study participants of The Multiethnic Cohort, who were aged 60 to 65 years, of European or Japanese descent, and with a body mass index (calculated as kg/m(2)) between 18.5 and 40. Dual-energy x-ray absorptiometry and abdominal magnetic resonance imaging scans were used to measure adiposity. After adjustments for age, ethnicity, and total fat mass, the FTO variants showed an association with less abdominal subcutaneous fat and a higher visceral-to-subcutaneous abdominal fat ratio, with the variant rs9941349 showing significant associations most consistently (P=0.003 and 0.03, respectively). Similarly, the LEPR rs1137101 variant was associated with less subcutaneous fat (P=0.01) and a greater visceral-to-subcutaneous fat ratio (P=0.03) and percent liver fat (P=0.007). MSRA rs545854 variant carriers had a lower percent of leg fat. Our findings provide initial evidence that some of the genetic risk factors identified for larger waist size might also contribute to disproportionately greater intra-abdominal and liver fat distribution in postmenopausal women. If replicated, these genetic variants can be incorporated with other biomarkers to predict high-risk body fat distribution. J Acad Nutr Diet. 2012;112:1048-1055.
引用
收藏
页码:1048 / 1055
页数:8
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