Association of the estrogen receptor-α gene with the metabolic syndrome and its component traits in African-American families -: The Insulin Resistance Atherosclerosis Family Study

被引:63
作者
Gallagher, Carla J.
Langefeld, Carl D.
Gordon, Candace J.
Campbell, Joel K.
Mychalecky, Josyf C.
Bryer-Ash, Michael
Rich, Stephen S.
Bowden, Donald W.
Sale, Michele M.
机构
[1] Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA 22908 USA
[2] Wake Forest Univ, Sch Med, Dept Biochem, Winston Salem, NC 27109 USA
[3] Wake Forest Univ, Ctr Human Genom, Winston Salem, NC 27109 USA
[4] Penn State Coll Med, Dept Hlth Evaluat Sci, Hershey, PA USA
[5] Wake Forest Univ, Sch Med, Div Publ Hlth Sci, Winston Salem, NC 27109 USA
[6] Wake Forest Univ, Sch Med, Dept Internal Med, Winston Salem, NC 27109 USA
[7] Univ Virginia, Dept Publ Hlth Sci, Charlottesville, VA USA
[8] Univ Calif Los Angeles, Div Endocrinol Diabet & Metab, David Geffen Sch Med, Los Angeles, CA USA
[9] Univ Virginia, Dept Med, Charlottesville, VA USA
[10] Univ Virginia, Dept Biochem & Mol Genet, Charlottesville, VA USA
关键词
D O I
10.2337/db06-1017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-We previously detected an association between a region of the estrogen receptor-alpha (ESR1) gene and type 2 diabetes in an African-American case-control study; thus, we investigated this region for associations with the metabolic syndrome and its component traits in African-American families from the Insulin Resistance Atherosclerosis Family Study. Research design and methods-A total of 17 single nucleotide polymorphisms (SNPs) from a contiguous 41-kb intron 1-intron 2 region of the ESR1 gene were genotyped in 548 individuals from 42 African-American pedigrees. Generalized estimating equations were computed using a sandwich estimator of the variance and exchangeable correlation to account for familial correlation. Results-Significant associations were detected between ESR1 SNPs and the metabolic syndrome (P = 0.005 to P = 0.029), type 2 diabetes (P = 0.001), insulin sensitivity (P = 0.0005 to P = 0.023), fasting insulin (P = 0.022 to P = 0.033), triglycerides (P = 0.021), LDL (P = 0.016 to P = 0.034), cholesterol (P = 0.046), BMI (P = 0.016 to P = 0.035), waist circumference (P = 0.012 to P = 0.023), and subcutaneous adipose tissue area (P = 0.016). Conclusions-It appears likely that ESR1 contributes to type 2 diabetes and CVD risk via pleiotropic effects, leading to insulin resistance, a poor lipid profile, and obesity.
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收藏
页码:2135 / 2141
页数:7
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