Title
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Association study of polymorphisms in the SOST gene region and parameters of bone strength and body composition in both young and elderly men : data from the Odense Androgen Study
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Author
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Abstract
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By means of different genetic association studies the SOST gene, encoding sclerostin, has repeatedly been suggested to regulate bone mineral density (BMD) and osteoporosis susceptibility. This study aimed at a further understanding of the importance of two previously studied single-nucleotide polymorphisms in the SOST gene, rs10534024 (SRP3) and rs9902563 (SRP9), in the Odense Androgen Study (OAS) cohort. This cohort includes a total of 1,383 Danish men from two different age groups, 20-29 years (n = 783) and 60-74 years (n = 600), and is well characterized. Subjects were phenotyped for BMD at several sites and additionally for body composition and hip geometric parameters. In a combined analysis of the young and the elderly OAS, no associations were found for SRP3 either with BMD or with hip geometry. Instead, we found that this polymorphism had a relatively large effect on weight (-1.149 kg) and body mass index (-0.389 kg/m(2)) (P = 0.021 and 0.006 under a codominant model). For SRP9, a significant association was found for femoral neck BMD (+0.020 g/cm(2), P = 0.020) and a trend toward significance for hip geometry (buckling ratio of the narrow neck) but only when considering a recessive effect of the minor allele (C). No age-specific effects were found for either of the two SNPs. In summary, we are the first to find interesting associations between SRP3 and body composition. For SRP9, we replicated a site-specific association with femoral neck BMD. In addition, we report a novel association for this polymorphism with hip geometry. |
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Language
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English
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Source (journal)
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Calcified tissue international. - New York, N.Y., 1979, currens
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Publication
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New York, N.Y.
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2012
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ISSN
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0171-967X
[print]
1432-0827
[online]
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DOI
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10.1007/S00223-011-9546-5
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Volume/pages
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90
:1
(2012)
, p. 30-39
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ISI
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000299075100004
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Full text (Publisher's DOI)
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Full text (publisher's version - intranet only)
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