Article

A family-based association study identified CYP17 as a candidate gene for obesity susceptibility in Caucasians.

Key Laboratory of Biomedical Information Engineering, Ministry of Education and Institute of Molecular Genetics, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi, P.R. China.
Genetics and molecular research: GMR (impact factor: 1.18). 05/2012; 11(3):1967-74. DOI:10.4238/2012.May.22.1 pp.1967-74
Source: PubMed

ABSTRACT The cytochrome P450c17α gene (CYP17) encodes a key biosynthesis enzyme of estrogen, which is critical in regulating adipogenesis and adipocyte development in humans. We therefore hypothesized that CYP17 is a candidate gene for predicting obesity. In order to test this hypothesis, we performed a family-based association test to investigate the relationship between the CYP17 gene and obesity phenotypes in a large sample comprising 1873 subjects from 405 Caucasian nuclear families of European origin recruited by the Osteoporosis Research Center of Creighton University, USA. Both single SNPs and haplotypes were tested for associations with obesity-related phenotypes, including body mass index (BMI) and fat mass. We identified three SNPs to be significantly associated with BMI, including rs3740397, rs6163, and rs619824. We further characterized the linkage disequilibrium structure for CYP17 and found that the whole CYP17 gene was located in a single-linkage disequilibrium block. This block was observed to be significantly associated with BMI. A major haplotype in this block was significantly associated with both BMI and fat mass. In conclusion, we suggest that the CYP17 gene has an effect on obesity in the Caucasian population. Further independent studies will be needed to confirm our findings.

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Keywords

405 Caucasian nuclear families
 
adipocyte development
 
associations
 
body mass index
 
candidate gene
 
Creighton University
 
CYP17 gene
 
cytochrome P450c17α gene
 
estrogen
 
European origin recruited
 
family-based association test
 
independent studies
 
key biosynthesis enzyme
 
linkage disequilibrium structure
 
Osteoporosis Research Center
 
regulating adipogenesis
 
single SNPs
 
single-linkage disequilibrium block
 
USA
 
whole CYP17 gene
 

H Yan