Common Variants of Hepatocyte Nuclear Factor 1β Are Associated With Type 2 Diabetes in a Chinese Population
Common Variants of Hepatocyte Nuclear Factor 1β Are Associated With Type 2 Diabetes in a Chinese Population Congrong Wang , Cheng Hu , Rong Zhang , Yuqian Bao , Xiaojing Ma , Jingyi Lu , Wen Qin , Xinyu Shao , Junxi Lu , Jing Xu , Huijuan Lu , Kunsan Xiang and Weiping Jia Department of Endocrinology...
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Published in | Diabetes (New York, N.Y.) Vol. 58; no. 4; pp. 1023 - 1027 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Alexandria, VA
American Diabetes Association
01.04.2009
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Subjects | |
Online Access | Get full text |
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Summary: | Common Variants of Hepatocyte Nuclear Factor 1β Are Associated With Type 2 Diabetes in a Chinese Population
Congrong Wang ,
Cheng Hu ,
Rong Zhang ,
Yuqian Bao ,
Xiaojing Ma ,
Jingyi Lu ,
Wen Qin ,
Xinyu Shao ,
Junxi Lu ,
Jing Xu ,
Huijuan Lu ,
Kunsan Xiang and
Weiping Jia
Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai Diabetes
Institute, Shanghai Clinical Center for Diabetes, Shanghai, China.
Corresponding author: Weiping Jia, wpjia{at}sjtu.edu.cn .
C.W. and C.H. contributed equally to this article.
Abstract
OBJECTIVE Hepatocyte nuclear factor 1β (HNF1β) is a transcription factor that is critical for pancreatic cell formation and glucose
homeostasis. Previous studies have reported that common variants of HNF1 β were associated with type 2 diabetes in Caucasians and West Africans. However, analysis in the subjects from the Botnia
study and Malmö Preventive Project produced conflicting results, and the role for HNF1 β in type 2 diabetes susceptibility remains unclear. We therefore investigated common variants across the HNF1 β gene in a Chinese population.
RESEARCH DESIGN AND METHODS Fifteen tagging single nucleotide polymorphisms (SNPs) were analyzed for association with type 2 diabetes in subjects with
type 2 diabetes ( n = 1,859) and normal glucose regulation ( n = 1,785).
RESULTS Consistent with the initial study, we observed evidence that the risk G allele of rs4430796 in intron 2 was significantly
associated with type 2 diabetes (odds ratio 1.16 [95% CI 1.05–1.29], P = 0.0035, empirical P = 0.0475). Furthermore, the at-risk G allele was associated with earlier age at diagnosis in the type 2 diabetic subjects
( P = 0.0228).
CONCLUSIONS The result of this study provides evidence that variants in the HNF1 β region contribute to susceptibility to type 2 diabetes in the Chinese population.
Footnotes
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore
be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
Received August 4, 2008.
Accepted January 13, 2009.
Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work
is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
© 2009 by the American Diabetes Association. |
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Bibliography: | C.W. and C.H. contributed equally to this article. |
ISSN: | 0012-1797 1939-327X |
DOI: | 10.2337/db08-1064 |