dc.contributor.author | Moayyeri, A | es_ES |
dc.contributor.author | Hsu, YU | es_ES |
dc.contributor.author | Karasik, D | es_ES |
dc.contributor.author | Estrada, Karol | es_ES |
dc.contributor.author | Xiao, SM | es_ES |
dc.contributor.author | Nielson, C | es_ES |
dc.contributor.author | Srikanth, P | es_ES |
dc.contributor.author | Giroux, S | es_ES |
dc.contributor.author | Wilson, SG | es_ES |
dc.contributor.author | Zheng, HF | es_ES |
dc.contributor.author | Smith, AV | es_ES |
dc.contributor.author | Pye, SR | es_ES |
dc.contributor.author | Leo, Paul J. | es_ES |
dc.contributor.author | Teumer, A | es_ES |
dc.contributor.author | Hwang, JY | es_ES |
dc.contributor.author | Ohlsson, C | es_ES |
dc.contributor.author | McGuigan, F | es_ES |
dc.contributor.author | Minster, Rl | es_ES |
dc.contributor.author | Hayward, C | es_ES |
dc.contributor.author | Olmos Martínez, José Manuel | es_ES |
dc.contributor.author | González Macías, Jesús | es_ES |
dc.contributor.author | Hernández Hernández, José Luis | es_ES |
dc.contributor.author | Riancho Moral, José Antonio | es_ES |
dc.contributor.other | Universidad de Cantabria | es_ES |
dc.date.accessioned | 2017-01-04T09:12:41Z | |
dc.date.available | 2017-01-04T09:12:41Z | |
dc.date.issued | 2014 | es_ES |
dc.identifier.issn | 0964-6906 | es_ES |
dc.identifier.issn | 1460-2083 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10902/9918 | |
dc.description.abstract | Quantitative ultrasound of the heel captures heel bone properties that independently predict fracture risk and, with bone mineral density (BMD) assessed by X-ray (DXA), may be convenient alternatives for evaluating osteoporosis and fracture risk. We performed a meta-analysis of genome-wide association (GWA) studies to assess the genetic determinants of heel broadband ultrasound attenuation (BUA; n = 14 260), velocity of sound (VOS; n = 15 514) and BMD (n = 4566) in 13 discovery cohorts. Independent replication involved seven cohorts with GWA data (in silico n = 11 452) and new genotyping in 15 cohorts (de novo n = 24 902). In combined random effects, meta-analysis of the discovery and replication cohorts, nine single nucleotide polymorphisms (SNPs) had genome-wide significant (P < 5 × 10(-8)) associations with heel bone properties. Alongside SNPs within or near previously identified osteoporosis susceptibility genes including ESR1 (6q25.1: rs4869739, rs3020331, rs2982552), SPTBN1 (2p16.2: rs11898505), RSPO3 (6q22.33: rs7741021), WNT16 (7q31.31: rs2908007), DKK1 (10q21.1: rs7902708) and GPATCH1 (19q13.11: rs10416265), we identified a new locus on chromosome 11q14.2 (rs597319 close to TMEM135, a gene recently linked to osteoblastogenesis and longevity) significantly associated with both BUA and VOS (P < 8.23 × 10(-14)). In meta-analyses involving 25 cohorts with up to 14 985 fracture cases, six of 10 SNPs associated with heel bone properties at P < 5 × 10(-6) also had the expected direction of association with any fracture (P < 0.05), including three SNPs with P < 0.005: 6q22.33 (rs7741021), 7q31.31 (rs2908007) and 10q21.1 (rs7902708). In conclusion, this GWA study reveals the effect of several genes common to central DXA-derived BMD and heel ultrasound/DXA measures and points to a new genetic locus with potential implications for better understanding of osteoporosis pathophysiology. | es_ES |
dc.format.extent | 15 p. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Oxford University Press | es_ES |
dc.rights | Atribución-NoComercial 3.0 España | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/3.0/es/ | * |
dc.source | Hum Mol Genet. 2014 Jun 1;23(11):3054-68 | es_ES |
dc.title | Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.rights.accessRights | openAccess | es_ES |
dc.identifier.DOI | 10.1093/hmg/ddt675 | es_ES |
dc.type.version | publishedVersion | es_ES |