Polymorphisms in the Selenoprotein S gene and subclinical cardiovascular disease in the Diabetes Heart Study
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- 作者：Amanda. J. Cox (1) (2) (3)
Allison B. Lehtinen (1) (2) (3)
Jianzhao Xu (1) (2)
Carl D. Langefeld (4)
Barry I. Freedman (5)
J. Jeffrey Carr (6)
Donald W. Bowden (1) (2) (3) - 关键词：Genetics ; Atherosclerosis ; Calcified plaque ; Diabetes mellitus
- 刊名：Acta Diabetologica
- 出版年：2013
- 出版时间：June 2013
- 年：2013
- 卷：50
- 期：3
- 页码：391-399
- 全文大小：277KB
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Allison B. Lehtinen (1) (2) (3)
Jianzhao Xu (1) (2)
Carl D. Langefeld (4)
Barry I. Freedman (5)
J. Jeffrey Carr (6)
Donald W. Bowden (1) (2) (3)
1. Center for Human Genomics, Wake Forest School of Medicine, Winston-Salem, NC, USA
2. Center for Diabetes Research, Wake Forest School of Medicine, Winston-Salem, NC, USA
3. Department of Biochemistry, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, 27157, USA
4. Department of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA
5. Department of Internal Medicine–Nephrology, Wake Forest School of Medicine, Winston-Salem, NC, USA
6. Department of Radiologic Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA - ISSN：1432-5233
文摘
Selenoprotein S (SelS) has previously been associated with a range of inflammatory markers, particularly in the context of cardiovascular disease (CVD). The aim of this study was to examine the role of SELS genetic variants in risk for subclinical CVD and mortality in individuals with type 2 diabetes mellitus (T2DM). The association between 10 polymorphisms tagging SELS and coronary (CAC), carotid (CarCP) and abdominal aortic calcified plaque, carotid intima media thickness and other known CVD risk factors was examined in 1220 European Americans from the family-based Diabetes Heart Study. The strongest evidence of association for SELS SNPs was observed for CarCP; rs28665122 (5-region; β?=?0.329, p?=?0.044), rs4965814 (intron 5; β?=?0.329, p?=?0.036), rs28628459 (3-region; β?=?0.331, p?=?0.039) and rs7178239 (downstream; β?=?0.375, p?=?0.016) were all associated. In addition, rs12917258 (intron 5) was associated with CAC (β?=??.230, p?=?0.032), and rs4965814, rs28628459 and rs9806366 were all associated with self-reported history of prior CVD (p?=?0.020-.043). These results suggest a potential role for the SELS region in the development subclinical CVD in this sample enriched for T2DM. Further understanding the mechanisms underpinning these relationships may prove important in predicting and managing CVD complications in T2DM.