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Assessment of sex-specific genetic and environmental effects on bone mineral density

dc.contributor.authorBrown, Lillian B.en_US
dc.contributor.authorStreeten, Elizabeth A.en_US
dc.contributor.authorShuldiner, Alan R.en_US
dc.contributor.authorAlmasy, Laura A.en_US
dc.contributor.authorPeyser, Patricia A.en_US
dc.contributor.authorMitchell, Braxton D.en_US
dc.date.accessioned2006-04-19T13:59:37Z
dc.date.available2006-04-19T13:59:37Z
dc.date.issued2004-09en_US
dc.identifier.citationBrown, Lillian B.; Streeten, Elizabeth A.; Shuldiner, Alan R.; Almasy, Laura A.; Peyser, Patricia A.; Mitchell, Braxton D. (2004)."Assessment of sex-specific genetic and environmental effects on bone mineral density." Genetic Epidemiology 27(2): 153-161. <http://hdl.handle.net/2027.42/34937>en_US
dc.identifier.issn0741-0395en_US
dc.identifier.issn1098-2272en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34937
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=15305331&dopt=citationen_US
dc.description.abstractAlthough it is widely accepted that genes contribute significantly to the variation in bone mineral density (BMD), the nature of the genetic contribution is poorly defined. There are large gender differences in BMD, although whether sex-specific genetic effects influencing variation in BMD contribute to these differences is not known. To address this issue, we studied 929 subjects from large families participating in the Amish Family Osteoporosis Study. Bone mineral density was measured at the hip and spine by dual energy x-ray absorptiometry (DXA). We used variance decomposition procedures to partition variation in BMD into genetic and environmental effects common to both sexes and to men and women separately. After accounting for covariate effects, the heritability of BMD ranged from 0.63 to 0.72 in men and 0.80 to 0.87 in women. The residual environmental variance in BMD at the spine, but not hip, was significantly higher in men than in women ( P < 0.05), reflecting a greater variance in BMD due to unexplained non-genetic factors in men. In contrast, there were no significant differences between men and women in the magnitude of the genetic variance in BMD, nor did the genetic correlation in BMD between men and women differ significantly from one. Overall, these analyses do not provide evidence for sex-specific genetic effects, suggesting that many of the genes influencing variation in BMD should be detectable in both men and women. © 2004 Wiley-Liss, Inc.en_US
dc.format.extent115315 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleAssessment of sex-specific genetic and environmental effects on bone mineral densityen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Epidemiology, University of Michigan School of Public Health, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Epidemiology, University of Michigan School of Public Health, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDivision of Endocrinology, Diabetes and Nutrition, University of Maryland School of Medicine, Baltimore, Marylanden_US
dc.contributor.affiliationotherDivision of Endocrinology, Diabetes and Nutrition, University of Maryland School of Medicine, Baltimore, Maryland ; Geriatric Research and Education Clinical Center (GRECC), Veterans Administration Medical Center, Baltimore, Marylanden_US
dc.contributor.affiliationotherDepartment of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Texasen_US
dc.contributor.affiliationotherDivision of Endocrinology, Diabetes and Nutrition, University of Maryland School of Medicine, Baltimore, Maryland ; Division of Endocrinology, Diabetes and Nutrition, University of Maryland School of Medicine, 660 W. Redwood Street, Room 492, Baltimore, MD 21201en_US
dc.identifier.pmid15305331en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34937/1/20009_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/gepi.20009en_US
dc.identifier.sourceGenetic Epidemiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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