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- Publisher Website: 10.1159/000112370
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- PMID: 18073493
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Article: Association of low-density lipoprotein receptor-related protein 5 (LRP5) promoter SNP with peak bone mineral density in Chinese women
Title | Association of low-density lipoprotein receptor-related protein 5 (LRP5) promoter SNP with peak bone mineral density in Chinese women |
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Authors | |
Keywords | Association study BMD Chinese Genetic association LRP5 Osteoporosis SNP |
Issue Date | 2008 |
Publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/HHE |
Citation | Human Heredity, 2008, v. 65 n. 4, p. 232-239 How to Cite? |
Abstract | Objective: Low-density lipoprotein receptor-related protein 5 (LRP5) is important for osteoblast differentiation and mutations of the gene are associated with both low and high bone mass syndromes. Our study aimed to evaluate the importance of LRP5 in the determination of peak bone mass acquisition in Chinese females in the general population. Methods: A total of 286 young southern Chinese females (aged 22-44 years) with low bone mineral density (BMD) (defined by a BMD Z score ≤-1.28 at either the hip or spine) or high BMD (Z score ≥+1) were studied. The LRP5 gene was sequenced for single nucleotide polymorphisms (SNPs) and 4 SNPs were tagged from 8 genotyped SNPs for this study. Results: Single locus allele association tests revealed significant associations of rs682429 and rs686921 with BMD variation (p < 0.05). Omnibus test (likelihood ratio test) revealed overall significant association between LRP5 gene locus and total hip BMD, with rs682429 being most predictive. rs682429 is located in 5′UTR, 2 bases adjacent to a consensus recognition site for the Elk-1 binding element. Conclusion: Common variations of the LRP5 promoter are associated with BMD in young women. These significant associations appear to be driven by rs682429. Functional studies are necessary to elucidate the role of this SNP on the effect of Elk-1 binding element transcriptional activity of LRP5 gene. Copyright © 2007 S. Karger AG. |
Persistent Identifier | http://hdl.handle.net/10722/76375 |
ISSN | 2023 Impact Factor: 1.1 2023 SCImago Journal Rankings: 0.483 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cheung, CL | en_HK |
dc.contributor.author | Huang, QY | en_HK |
dc.contributor.author | Chan, V | en_HK |
dc.contributor.author | Kung, AWC | en_HK |
dc.date.accessioned | 2010-09-06T07:20:33Z | - |
dc.date.available | 2010-09-06T07:20:33Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Human Heredity, 2008, v. 65 n. 4, p. 232-239 | en_HK |
dc.identifier.issn | 0001-5652 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/76375 | - |
dc.description.abstract | Objective: Low-density lipoprotein receptor-related protein 5 (LRP5) is important for osteoblast differentiation and mutations of the gene are associated with both low and high bone mass syndromes. Our study aimed to evaluate the importance of LRP5 in the determination of peak bone mass acquisition in Chinese females in the general population. Methods: A total of 286 young southern Chinese females (aged 22-44 years) with low bone mineral density (BMD) (defined by a BMD Z score ≤-1.28 at either the hip or spine) or high BMD (Z score ≥+1) were studied. The LRP5 gene was sequenced for single nucleotide polymorphisms (SNPs) and 4 SNPs were tagged from 8 genotyped SNPs for this study. Results: Single locus allele association tests revealed significant associations of rs682429 and rs686921 with BMD variation (p < 0.05). Omnibus test (likelihood ratio test) revealed overall significant association between LRP5 gene locus and total hip BMD, with rs682429 being most predictive. rs682429 is located in 5′UTR, 2 bases adjacent to a consensus recognition site for the Elk-1 binding element. Conclusion: Common variations of the LRP5 promoter are associated with BMD in young women. These significant associations appear to be driven by rs682429. Functional studies are necessary to elucidate the role of this SNP on the effect of Elk-1 binding element transcriptional activity of LRP5 gene. Copyright © 2007 S. Karger AG. | en_HK |
dc.language | eng | en_HK |
dc.publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/HHE | en_HK |
dc.relation.ispartof | Human Heredity | en_HK |
dc.rights | Human Heredity. Copyright © S Karger AG. | en_HK |
dc.subject | Association study | en_HK |
dc.subject | BMD | en_HK |
dc.subject | Chinese | en_HK |
dc.subject | Genetic association | en_HK |
dc.subject | LRP5 | en_HK |
dc.subject | Osteoporosis | en_HK |
dc.subject | SNP | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Asian Continental Ancestry Group - genetics | en_HK |
dc.subject.mesh | Bone Density - genetics | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Femur Neck - physiology | en_HK |
dc.subject.mesh | Gene Frequency | en_HK |
dc.subject.mesh | Genotype | en_HK |
dc.subject.mesh | Hip - physiology | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | LDL-Receptor Related Proteins - genetics | en_HK |
dc.subject.mesh | Linkage Disequilibrium | en_HK |
dc.subject.mesh | Low Density Lipoprotein Receptor-Related Protein-5 | en_HK |
dc.subject.mesh | Lumbar Vertebrae - physiology | en_HK |
dc.subject.mesh | Polymorphism, Single Nucleotide | en_HK |
dc.subject.mesh | Promoter Regions, Genetic - genetics | en_HK |
dc.subject.mesh | Sequence Analysis, DNA | en_HK |
dc.title | Association of low-density lipoprotein receptor-related protein 5 (LRP5) promoter SNP with peak bone mineral density in Chinese women | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0001-5652&volume=65&issue=4&spage=232&epage=239&date=2007&atitle=Association+of+low-density+lipoprotein+receptor-related+protein+5+(LRP5)+promoter+SNP+with+peak+bone+mineral+density+in+Chinese+women. | en_HK |
dc.identifier.email | Cheung, CL: lung1212@hku.hk | en_HK |
dc.identifier.email | Huang, QY: qyhuang@hotmail.com | en_HK |
dc.identifier.email | Chan, V: vnychana@hkucc.hku.hk | en_HK |
dc.identifier.email | Kung, AWC: awckung@hku.hk | en_HK |
dc.identifier.authority | Cheung, CL=rp01749 | en_HK |
dc.identifier.authority | Huang, QY=rp00521 | en_HK |
dc.identifier.authority | Chan, V=rp00320 | en_HK |
dc.identifier.authority | Kung, AWC=rp00368 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1159/000112370 | en_HK |
dc.identifier.pmid | 18073493 | - |
dc.identifier.scopus | eid_2-s2.0-38649109162 | en_HK |
dc.identifier.hkuros | 141387 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-38649109162&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 65 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 232 | en_HK |
dc.identifier.epage | 239 | en_HK |
dc.identifier.isi | WOS:000252877500006 | - |
dc.publisher.place | Switzerland | en_HK |
dc.identifier.scopusauthorid | Cheung, CL=14520953400 | en_HK |
dc.identifier.scopusauthorid | Huang, QY=7403630787 | en_HK |
dc.identifier.scopusauthorid | Chan, V=7202654865 | en_HK |
dc.identifier.scopusauthorid | Kung, AWC=7102322339 | en_HK |
dc.identifier.issnl | 0001-5652 | - |