Polymorphisms in Wnt signaling pathway genes are associated with peak bone mineral density, lean mass, and fat mass in Chinese male nuclear families

Summary Our objective was to investigate the associations between polymorphisms in Wnt pathway genes and peak bone mineral density (BMD) and body composition in young Chinese men. Our study identified that WNT5B and CTNNBL1 for both BMD and body composition, and WNT4 and CTNNB1 gene polymorphisms co...

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Veröffentlicht in:Osteoporosis international 2016-05, Vol.27 (5), p.1805-1815
Hauptverfasser: Zheng, Y., Wang, C., Zhang, H., Shao, C., Gao, L.-H., Li, S.-S., Yu, W.-J., He, J.-W., Fu, W.-Z., Hu, Y.-Q., Li, M., Liu, Y.-J., Zhang, Z.-L.
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Sprache:eng
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Zusammenfassung:Summary Our objective was to investigate the associations between polymorphisms in Wnt pathway genes and peak bone mineral density (BMD) and body composition in young Chinese men. Our study identified that WNT5B and CTNNBL1 for both BMD and body composition, and WNT4 and CTNNB1 gene polymorphisms contribute to the variation in BMD and body composition in young Chinese men, respectively. Introduction Our objective was to investigate the associations between polymorphisms in WNT4 , WNT5B , WNT10B , WNT16 , CTNNB1 , and CTNNBL1 genes and peak bone mineral density (BMD), lean mass (LM), and fat mass (FM) in young Chinese men. Methods Using SNPscan TM kits, 51 single-nucleotide polymorphisms (SNPs) located in the 6 genes were genotyped in a total of 1214 subjects from 399 Chinese nuclear families. BMD, total lean mass (TLM), and total fat mass (TFM) were measured using dual energy X-ray absorptiometry (DXA). The associations between the 51 SNPs and peak BMD and body composition [including the TLM, percentage lean mass (PLM), TFM, percentage fat mass (PFM), and the body mass index (BMI)] were analyzed through quantitative transmission disequilibrium tests (QTDTs). Results For peak BMD, we found significant within-family associations of rs2240506, rs7308793, and rs4765830 in the WNT5B gene and rs10917157 in the WNT4 gene with the lumbar spine BMD (all P  
ISSN:0937-941X
1433-2965
DOI:10.1007/s00198-015-3457-7