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dc.contributor.authorKiel, Douglas Pen_US
dc.contributor.authorDemissie, Serkalemen_US
dc.contributor.authorDupuis, Joséeen_US
dc.contributor.authorLunetta, Kathryn Len_US
dc.contributor.authorMurabito, Joanne Men_US
dc.contributor.authorKarasik, Daviden_US
dc.date.accessioned2011-12-29T21:02:17Z
dc.date.available2011-12-29T21:02:17Z
dc.date.copyright2007
dc.date.issued2007-9-19
dc.identifier.citationKiel, Douglas P, Serkalem Demissie, Josée Dupuis, Kathryn L Lunetta, Joanne M Murabito, David Karasik. "Genome-wide association with bone mass and geometry in the Framingham Heart Study." BMC Medical Genetics 8 (Suppl 1):S14. (2007)
dc.identifier.issn1471-2350
dc.identifier.urihttps://hdl.handle.net/2144/2503
dc.description.abstractBACKGROUND: Osteoporosis is characterized by low bone mass and compromised bone structure, heritable traits that contribute to fracture risk. There have been no genome-wide association and linkage studies for these traits using high-density genotyping platforms. METHODS: We used the Affymetrix 100K SNP GeneChip marker set in the Framingham Heart Study (FHS) to examine genetic associations with ten primary quantitative traits: bone mineral density (BMD), calcaneal ultrasound, and geometric indices of the hip. To test associations with multivariable-adjusted residual trait values, we used additive generalized estimating equation (GEE) and family-based association tests (FBAT) models within each sex as well as sexes combined. We evaluated 70,987 autosomal SNPs with genotypic call rates ≥80%, HWE p ≥ 0.001, and MAF ≥10% in up to 1141 phenotyped individuals (495 men and 646 women, mean age 62.5 yrs). Variance component linkage analysis was performed using 11,200 markers. RESULTS: Heritability estimates for all bone phenotypes were 30–66%. LOD scores ≥3.0 were found on chromosomes 15 (1.5 LOD confidence interval: 51,336,679–58,934,236 bp) and 22 (35,890,398–48,603,847 bp) for femoral shaft section modulus. The ten primary phenotypes had 12 associations with 100K SNPs in GEE models at p < 0.000001 and 2 associations in FBAT models at p < 0.000001. The 25 most significant p-values for GEE and FBAT were all less than 3.5 × 10-6 and 2.5 × 10-5, respectively. Of the 40 top SNPs with the greatest numbers of significantly associated BMD traits (including femoral neck, trochanter, and lumbar spine), one half to two-thirds were in or near genes that have not previously been studied for osteoporosis. Notably, pleiotropic associations between BMD and bone geometric traits were uncommon. Evidence for association (FBAT or GEE p < 0.05) was observed for several SNPs in candidate genes for osteoporosis, such as rs1801133 in MTHFR; rs1884052 and rs3778099 in ESR1; rs4988300 in LRP5; rs2189480 in VDR; rs2075555 in COLIA1; rs10519297 and rs2008691 in CYP19, as well as SNPs in PPARG (rs10510418 and rs2938392) and ANKH (rs2454873 and rs379016). All GEE, FBAT and linkage results are provided as an open-access results resource at. CONCLUSION: The FHS 100K SNP project offers an unbiased genome-wide strategy to identify new candidate loci and to replicate previously suggested candidate genes for osteoporosis.en_US
dc.description.sponsorshipFramingham Heart Study of the National Heart, Lung, and Blood Institute of the National Institutes of Health (N01-HC-25195; Boston University School of Medicine; National Institute of Arthritis, Musculoskeletal and Skin Diseases and the National Institute on Aging (R01 AR/AG 41398, R01 AR050066)en_US
dc.language.isoen
dc.publisherBioMed Centralen_US
dc.rightsCopyright 2007 Kiel et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution 2.0 License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0
dc.titleGenome-Wide Association with Bone Mass and Geometry in the Framingham Heart Studyen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/1471-2350-8-S1-S14
dc.identifier.pmid17903296
dc.identifier.pmcid1995606


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Copyright 2007 Kiel et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution 2.0 License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as Copyright 2007 Kiel et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution 2.0 License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.