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- Publisher Website: 10.1093/ndt/gfp661
- Scopus: eid_2-s2.0-77951694421
- PMID: 20031928
- WOS: WOS:000276994400033
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Article: Variation in IGHMBP2 is not associated with IgA nephropathy in independent studies of UK Caucasian and Chinese Han patients
Title | Variation in IGHMBP2 is not associated with IgA nephropathy in independent studies of UK Caucasian and Chinese Han patients |
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Authors | |
Keywords | Caucasian Chinese Genetic association study IgA nephropathy IGHMBP2 |
Issue Date | 2010 |
Publisher | Oxford University Press. The Journal's web site is located at http://ndt.oxfordjournals.org/ |
Citation | Nephrology Dialysis Transplantation, 2010, v. 25 n. 5, p. 1547-1554 How to Cite? |
Abstract | Background. IgA nephropathy is a major cause of end-stage renal disease worldwide. Its aetiology is poorly understood but there is good evidence for a major genetic component, although to date, no gene has been conclusively identified. We describe a new UK multicentre DNA collection assembled to investigate this. A Japanese genome-wide analysis recently reported that common genetic variation in immunoglobulin mu-binding protein 2 (IGHMBP2) was associated with IgA nephropathy. We sought to replicate this using the new UK collection, and through an independent parallel analysis of a Han Chinese population.Methods. In the UK collection, haplotype-tagging (tag) single-nucleotide polymorphisms (SNPs) and haplotypes were analysed in a case-control study (349 cases, 605 controls) and family-based analysis (162 complete and 23 partially complete family trios), which was performed using the transmission disequilibrium test. In parallel, 663 cases of IgA nephropathy and 663 controls from a Chinese population were analysed: coding and flanking regions of the gene were re-sequenced in a subset, and SNP and haplotype association analysis was performed in the whole collection using the identified tagSNPs and all the coding and exonic flanking SNPs.Results. Case-control studies in UK and Chinese populations, and family-based tests in the UK population provided no evidence for association between variation in IGHMBP2 and IgA nephropathy. The A allele of SNP G34448A was not present in the UK collection. It was present but not associated with the disease in the Chinese population.Conclusion. Variation in IGHMBP2 does not confer significant susceptibility to IgA nephropathy in UK Caucasian or Chinese Han populations. © The Author 2009. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/163311 |
ISSN | 2023 Impact Factor: 4.8 2023 SCImago Journal Rankings: 1.414 |
ISI Accession Number ID | |
References | |
Errata |
DC Field | Value | Language |
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dc.contributor.author | Lou, T | en_HK |
dc.contributor.author | Zhang, J | en_HK |
dc.contributor.author | Gale, DP | en_HK |
dc.contributor.author | Rees, AJ | en_HK |
dc.contributor.author | Rhodes, B | en_HK |
dc.contributor.author | Feehally, J | en_HK |
dc.contributor.author | Li, C | en_HK |
dc.contributor.author | Li, Y | en_HK |
dc.contributor.author | Li, R | en_HK |
dc.contributor.author | Huang, W | en_HK |
dc.contributor.author | Hu, B | en_HK |
dc.contributor.author | Leung, JCK | en_HK |
dc.contributor.author | Lam, MF | en_HK |
dc.contributor.author | Lai, KN | en_HK |
dc.contributor.author | Wang, Y | en_HK |
dc.contributor.author | Maxwell, PH | en_HK |
dc.date.accessioned | 2012-09-05T05:29:57Z | - |
dc.date.available | 2012-09-05T05:29:57Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Nephrology Dialysis Transplantation, 2010, v. 25 n. 5, p. 1547-1554 | en_HK |
dc.identifier.issn | 0931-0509 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/163311 | - |
dc.description.abstract | Background. IgA nephropathy is a major cause of end-stage renal disease worldwide. Its aetiology is poorly understood but there is good evidence for a major genetic component, although to date, no gene has been conclusively identified. We describe a new UK multicentre DNA collection assembled to investigate this. A Japanese genome-wide analysis recently reported that common genetic variation in immunoglobulin mu-binding protein 2 (IGHMBP2) was associated with IgA nephropathy. We sought to replicate this using the new UK collection, and through an independent parallel analysis of a Han Chinese population.Methods. In the UK collection, haplotype-tagging (tag) single-nucleotide polymorphisms (SNPs) and haplotypes were analysed in a case-control study (349 cases, 605 controls) and family-based analysis (162 complete and 23 partially complete family trios), which was performed using the transmission disequilibrium test. In parallel, 663 cases of IgA nephropathy and 663 controls from a Chinese population were analysed: coding and flanking regions of the gene were re-sequenced in a subset, and SNP and haplotype association analysis was performed in the whole collection using the identified tagSNPs and all the coding and exonic flanking SNPs.Results. Case-control studies in UK and Chinese populations, and family-based tests in the UK population provided no evidence for association between variation in IGHMBP2 and IgA nephropathy. The A allele of SNP G34448A was not present in the UK collection. It was present but not associated with the disease in the Chinese population.Conclusion. Variation in IGHMBP2 does not confer significant susceptibility to IgA nephropathy in UK Caucasian or Chinese Han populations. © The Author 2009. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. | en_HK |
dc.language | eng | en_US |
dc.publisher | Oxford University Press. The Journal's web site is located at http://ndt.oxfordjournals.org/ | en_HK |
dc.relation.ispartof | Nephrology Dialysis Transplantation | en_HK |
dc.subject | Caucasian | en_HK |
dc.subject | Chinese | en_HK |
dc.subject | Genetic association study | en_HK |
dc.subject | IgA nephropathy | en_HK |
dc.subject | IGHMBP2 | en_HK |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Asian Continental Ancestry Group - Genetics | en_US |
dc.subject.mesh | Dna-Binding Proteins - Genetics | en_US |
dc.subject.mesh | Databases, Genetic | en_US |
dc.subject.mesh | European Continental Ancestry Group - Genetics | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Glomerulonephritis, Iga - Genetics | en_US |
dc.subject.mesh | Great Britain | en_US |
dc.subject.mesh | Haplotypes | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Linkage Disequilibrium | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Polymorphism, Single Nucleotide | en_US |
dc.subject.mesh | Transcription Factors - Genetics | en_US |
dc.title | Variation in IGHMBP2 is not associated with IgA nephropathy in independent studies of UK Caucasian and Chinese Han patients | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Leung, JCK: jckleung@hku.hk | en_HK |
dc.identifier.email | Lai, KN: knlai@hku.hk | en_HK |
dc.identifier.authority | Leung, JCK=rp00448 | en_HK |
dc.identifier.authority | Lai, KN=rp00324 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1093/ndt/gfp661 | en_HK |
dc.identifier.pmid | 20031928 | - |
dc.identifier.scopus | eid_2-s2.0-77951694421 | en_HK |
dc.identifier.hkuros | 180808 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77951694421&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 25 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 1547 | en_HK |
dc.identifier.epage | 1554 | en_HK |
dc.identifier.isi | WOS:000276994400033 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.relation.erratum | doi:10.1093/ndt/gfq312 | - |
dc.identifier.scopusauthorid | Lou, T=7004047319 | en_HK |
dc.identifier.scopusauthorid | Zhang, J=7601342172 | en_HK |
dc.identifier.scopusauthorid | Gale, DP=22634019700 | en_HK |
dc.identifier.scopusauthorid | Rees, AJ=7201968937 | en_HK |
dc.identifier.scopusauthorid | Rhodes, B=24076981400 | en_HK |
dc.identifier.scopusauthorid | Feehally, J=7005075936 | en_HK |
dc.identifier.scopusauthorid | Li, C=26663041900 | en_HK |
dc.identifier.scopusauthorid | Li, Y=8930727500 | en_HK |
dc.identifier.scopusauthorid | Li, R=55491291300 | en_HK |
dc.identifier.scopusauthorid | Huang, W=10041590500 | en_HK |
dc.identifier.scopusauthorid | Hu, B=36087575900 | en_HK |
dc.identifier.scopusauthorid | Leung, JCK=7202180349 | en_HK |
dc.identifier.scopusauthorid | Lam, MF=35300050600 | en_HK |
dc.identifier.scopusauthorid | Lai, KN=7402135706 | en_HK |
dc.identifier.scopusauthorid | Wang, Y=36088373700 | en_HK |
dc.identifier.scopusauthorid | Maxwell, PH=35399996300 | en_HK |
dc.identifier.issnl | 0931-0509 | - |