File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1007/s00774-004-0607-y
- Scopus: eid_2-s2.0-21044450680
- PMID: 15981030
- WOS: WOS:000230069500009
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Association and linkage analyses of interleukin-6 gene 634C/G polymorphism and bone phenotypes in Chinese
Title | Association and linkage analyses of interleukin-6 gene 634C/G polymorphism and bone phenotypes in Chinese |
---|---|
Authors | |
Keywords | Bone mineral density Bone size Interleukin-6 gene Linkage Transmission disequilibrium test |
Issue Date | 2005 |
Publisher | Springer Japan. The Journal's web site is located at http://link.springer.de/link/service/journals/00774/index.htm |
Citation | Journal Of Bone And Mineral Metabolism, 2005, v. 23 n. 4, p. 323-328 How to Cite? |
Abstract | In this study, we tested the interleukin-6 (IL-6) gene as an important candidate gene for its linkage and association with the variation of bone phenotypes (bone mineral density [BMD] and bone size) in young Chinese female subjects. We genotyped the IL-6 gene at the -634C/G restriction fragment length polymorphism (RFLP) site (ID, RS1800796) in 1263 individuals from 402 Chinese nuclear families, composed of both parents and at least one healthy daughter (mean age ± SD, 31.4 ± 5.8 years). Using the daughters' bone phenotypes, we tested total-family association, within-family association (via transmission disequilibrium test, [TDT]), and linkage, between the -634C/G marker and bone phenotypes at the spine and the hip. No significant association or linkage was found for bone size and BMD, although a trend was observed for linkage between the IL-6 gene -634C/G marker and L1-4 spinal BMD (adjusted for age, weight, and height). Our results, together with the findings from other studies, indicate that the IL-6 gene, although important for postmenopausal bone loss, may have a limited impact on peak bone mass variation in a Chinese population. © Springer-Verlag 2005. |
Persistent Identifier | http://hdl.handle.net/10722/181198 |
ISSN | 2023 Impact Factor: 2.4 2023 SCImago Journal Rankings: 0.766 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lei, SF | en_US |
dc.contributor.author | Liu, YZ | en_US |
dc.contributor.author | Deng, FY | en_US |
dc.contributor.author | Li, YM | en_US |
dc.contributor.author | Li, MX | en_US |
dc.contributor.author | Deng, HW | en_US |
dc.date.accessioned | 2013-02-21T02:02:43Z | - |
dc.date.available | 2013-02-21T02:02:43Z | - |
dc.date.issued | 2005 | en_US |
dc.identifier.citation | Journal Of Bone And Mineral Metabolism, 2005, v. 23 n. 4, p. 323-328 | en_US |
dc.identifier.issn | 0914-8779 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/181198 | - |
dc.description.abstract | In this study, we tested the interleukin-6 (IL-6) gene as an important candidate gene for its linkage and association with the variation of bone phenotypes (bone mineral density [BMD] and bone size) in young Chinese female subjects. We genotyped the IL-6 gene at the -634C/G restriction fragment length polymorphism (RFLP) site (ID, RS1800796) in 1263 individuals from 402 Chinese nuclear families, composed of both parents and at least one healthy daughter (mean age ± SD, 31.4 ± 5.8 years). Using the daughters' bone phenotypes, we tested total-family association, within-family association (via transmission disequilibrium test, [TDT]), and linkage, between the -634C/G marker and bone phenotypes at the spine and the hip. No significant association or linkage was found for bone size and BMD, although a trend was observed for linkage between the IL-6 gene -634C/G marker and L1-4 spinal BMD (adjusted for age, weight, and height). Our results, together with the findings from other studies, indicate that the IL-6 gene, although important for postmenopausal bone loss, may have a limited impact on peak bone mass variation in a Chinese population. © Springer-Verlag 2005. | en_US |
dc.language | eng | en_US |
dc.publisher | Springer Japan. The Journal's web site is located at http://link.springer.de/link/service/journals/00774/index.htm | en_US |
dc.relation.ispartof | Journal of Bone and Mineral Metabolism | en_US |
dc.subject | Bone mineral density | - |
dc.subject | Bone size | - |
dc.subject | Interleukin-6 gene | - |
dc.subject | Linkage | - |
dc.subject | Transmission disequilibrium test | - |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Bone Density - Genetics - Immunology | en_US |
dc.subject.mesh | Bone And Bones - Anatomy & Histology | en_US |
dc.subject.mesh | China | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Interleukin-6 - Genetics | en_US |
dc.subject.mesh | Linkage Disequilibrium | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Phenotype | en_US |
dc.subject.mesh | Polymorphism, Genetic | en_US |
dc.title | Association and linkage analyses of interleukin-6 gene 634C/G polymorphism and bone phenotypes in Chinese | en_US |
dc.type | Article | en_US |
dc.identifier.email | Li, MX: mxli@hku.hk | en_US |
dc.identifier.authority | Li, MX=rp01722 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1007/s00774-004-0607-y | en_US |
dc.identifier.pmid | 15981030 | - |
dc.identifier.scopus | eid_2-s2.0-21044450680 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-21044450680&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 23 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.spage | 323 | en_US |
dc.identifier.epage | 328 | en_US |
dc.identifier.isi | WOS:000230069500009 | - |
dc.publisher.place | Japan | en_US |
dc.identifier.scopusauthorid | Lei, SF=7102453442 | en_US |
dc.identifier.scopusauthorid | Liu, YZ=7410227746 | en_US |
dc.identifier.scopusauthorid | Deng, FY=19640145800 | en_US |
dc.identifier.scopusauthorid | Li, YM=7502098054 | en_US |
dc.identifier.scopusauthorid | Li, MX=17135391100 | en_US |
dc.identifier.scopusauthorid | Deng, HW=34568563000 | en_US |
dc.identifier.issnl | 0914-8779 | - |