Association study of common variants in the sFRP1 gene region and parameters of bone strength and body composition in two independent healthy Caucasian male cohorts

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• 作者：Eveline Boudin^a ; ^{eveline.boudin@ua.ac.be} ; Elke Piters^a ; ^{elke.piters@ua.ac.be} ; Erik Fransen^a ; ^{erik.fransen@ua.ac.be} ; Torben Leo Nielsen^b ; ^{torben@dsa-net.dk} ; ^{torben.nielsen@ouh.fyns-amt.dk} ; Marianne Andersen^b ; ^{marianne.andersen@ouh.regionsyddanmark.dk} ; ^{m.andersen@dadlnet.dk} ; Greet Roef^c ; ^{Greet.Roef@UGent.be} ; Youri Taes^c ; ^{youri.taes@UGent.be} ; Kim Brixen^b ; ^{kbrixen@health.sdu.dk} ; Wim Van Hul^a ; ^{wim.vanhul@ua.ac.be}
• 关键词：sFRP1 ; Osteoporosis ; Wnt signaling ; Association study ; Obesity
• 刊名：Molecular Genetics and Metabolism
• 出版年：2012
• 期刊代码：175_10967192
• 类别：bio
• 出版时间：March, 2012
• 卷：105
• 期：3
• 页码：508-515
• 文件大小：238 K

摘要

Bone mineral density (BMD) and bone strength are predictive parameters for the development of osteoporosis and related fracture later in life. Although it is well known that BMD and bone strength have a high heritability, not much of the variation is already explained. Mice models showed that sFRP1 has an influence on bone formation. Therefore this study aimed to investigate the effect of common genetic variation on BMD and bone strength in Caucasian men of different ages.

Using HapMap we selected 13 tagSNPs which tag most common genetic variation in and around sFRP1 and we genotyped these SNPs in the young cohort of the Odense Androgen Study (OAS). The OAS includes a total of 1383 Danish men from two different age groups ([20-29 years]: N = 783; [60-74 years]: N = 600) and is well characterised. The subjects were phenotyped for BMD at several sites, and additionally for body composition and hip geometry parameters. Based on the results of the young cohort we selected three SNPs for further analysis in the complete OAS population. To conclude we tried to replicate the results of two SNPs in an independent population of 994 Belgian men.

We found a strong association for rs9694405 with BMI as well in both cohorts separately as in the whole OAS population. Further we found rs4736965 associated with several hip geometry parameters in the same population. However we were not able to replicate those results in the Belgian population. At last we found in the OAS population age specific effects for rs10106678 with whole body BMD and waist to hip ratio.