Abstract | OBJECTIVE:
Hepatocyte nuclear factor 1beta (HNF1beta) is a transcription factor that is critical for pancreatic cell formation and glucose homeostasis. Previous studies have reported that common variants of HNF1beta 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 HNF1beta in type 2 diabetes susceptibility remains unclear. We therefore investigated common variants across the HNF1beta 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 HNF1beta region contribute to susceptibility to type 2 diabetes in the Chinese population.
|
Authors | Congrong Wang, Cheng Hu, Rong Zhang, Yuqian Bao, Xiaojing Ma, Jingyi Lu, Wen Qin, Xinyu Shao, Junxi Lu, Jing Xu, Huijuan Lu, Kunsan Xiang, Weiping Jia |
Journal | Diabetes
(Diabetes)
Vol. 58
Issue 4
Pg. 1023-7
(Apr 2009)
ISSN: 1939-327X [Electronic] United States |
PMID | 19168595
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Blood Glucose
- Hepatocyte Nuclear Factor 1-beta
|
Topics |
- Age of Onset
- Aged
- Asian People
(genetics)
- Black People
(genetics)
- Blood Glucose
- China
- Diabetes Mellitus, Type 2
(genetics)
- Female
- Genetic Predisposition to Disease
- Genetic Variation
- Hepatocyte Nuclear Factor 1-beta
(genetics)
- Humans
- Linkage Disequilibrium
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
- White People
(genetics)
|