Common polymorphisms in the adiponectin gene ACDC are not associated with diabetes in Pima Indians

被引:66
作者
de Courten, BV
Hanson, RL
Funahashi, T
Lindsay, RS
Matsuzawa, Y
Tanaka, S
Thameem, F
Gruber, JD
Froguel, P
Wolford, JK
机构
[1] Translat Genomics Res Inst, Diabet Res Unit, Phoenix, AZ USA
[2] NIDDK, Clin Diabet & Nutr Sect, NIH, Phoenix, AZ USA
[3] Osaka Univ, Grad Sch Med, Dept Internal Med & Mol Sci, Osaka, Japan
[4] Inst Pasteur, Inst Biol, CNRS, F-59019 Lille, France
基金
英国医学研究理事会;
关键词
D O I
10.2337/diabetes.54.1.284
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adiponectin is an abundant adipose tissue-derived protein with important metabolic effects. Plasma adiponectin levels are decreased in obese individuals, and low adiponectin levels predict insulin resistance and type 2 diabetes. Two variants in the adiponectin gene ACDC have been previously associated with plasma adiponectin levels, obesity, insulin resistance, and type 2 diabetes. To determine the role of genetic variation in ACDC in susceptibility to obesity and type 2 diabetes in Pima Indians, we screened the promoter, exons, and exonintron boundaries of the gene to identify allelic variants. We identified 17 informative polymorphisms that comprised four common (minor allele frequency > 15%) linkage disequilibrium clusters consisting of 1-4 variants each. We genotyped one representative polymorphism from each cluster in 1,338 individuals and assessed genotypic association with type 2 diabetes, BMI, serum lipid levels, serum adiponectin levels, and measures of insulin sensitivity and secretion. None of the ACDC variants were associated with type 2 diabetes, BMI, or measures of insulin sensitivity or secretion. One variant, single nucleotide polymorphism (SNP)12823, was associated with serum adiponectin levels (P = 0.002), but this association explained only 2% of the variance of serum adiponectin levels. Our findings suggest that these common ACDC polymorphisms do not play a major role in susceptibility to obesity or type 2 diabetes in this population.
引用
收藏
页码:284 / 289
页数:6
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