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Copy number variation of the Beta-defensin genes in europeans: no supporting evidence for association with lung function, chronic obstructive pulmonary disease or asthma

cris.virtualsource.author-orcid7413f69b-1d5b-413f-a43c-b62e915e5a4f
cris.virtualsource.author-orcid3857e2d3-2b7f-42b6-878d-ce868ac1673c
datacite.rightsopen.access
dc.contributor.authorWain, Louise V.
dc.contributor.authorOdenthal-Hesse, Linda
dc.contributor.authorAbujaber, Razan
dc.contributor.authorSayers, Ian
dc.contributor.authorBeardsmore, Caroline
dc.contributor.authorGaillard, Erol A.
dc.contributor.authorChappell, Sally
dc.contributor.authorDogaru, Cristian
dc.contributor.authorMcKeever, Tricia
dc.contributor.authorGuetta-Baranes, Tamar
dc.contributor.authorKalsheker, Noor
dc.contributor.authorKühni, Claudia
dc.contributor.authorHall, Ian P.
dc.contributor.authorTobin, Martin D.
dc.contributor.authorHollox, Edward J.
dc.date.accessioned2024-10-14T15:51:36Z
dc.date.available2024-10-14T15:51:36Z
dc.date.issued2014-01
dc.description.abstractLung function measures are heritable, predict mortality and are relevant in diagnosis of chronic obstructive pulmonary disease (COPD). COPD and asthma are diseases of the airways with major public health impacts and each have a heritable component. Genome-wide association studies of SNPs have revealed novel genetic associations with both diseases but only account for a small proportion of the heritability. Complex copy number variation may account for some of the missing heritability. A well-characterised genomic region of complex copy number variation contains beta-defensin genes (DEFB103, DEFB104 and DEFB4), which have a role in the innate immune response. Previous studies have implicated these and related genes as being associated with asthma or COPD. We hypothesised that copy number variation of these genes may play a role in lung function in the general population and in COPD and asthma risk. We undertook copy number typing of this locus in 1149 adult and 689 children using a paralogue ratio test and investigated association with COPD, asthma and lung function. Replication of findings was assessed in a larger independent sample of COPD cases and smoking controls. We found evidence for an association of beta-defensin copy number with COPD in the adult cohort (OR = 1.4, 95%CI:1.02-1.92, P = 0.039) but this finding, and findings from a previous study, were not replicated in a larger follow-up sample(OR = 0.89, 95%CI:0.72-1.07, P = 0.217). No robust evidence of association with asthma in children was observed. We found no evidence for association between beta-defensin copy number and lung function in the general populations. Our findings suggest that previous reports of association of beta-defensin copy number with COPD should be viewed with caution. Suboptimal measurement of copy number can lead to spurious associations. Further beta-defensin copy number measurement in larger sample sizes of COPD cases and children with asthma are needed.
dc.description.numberOfPages8
dc.description.sponsorshipInstitut für Sozial- und Präventivmedizin (ISPM)
dc.identifier.doi10.7892/boris.40721
dc.identifier.pmid24404154
dc.identifier.publisherDOI10.1371/journal.pone.0084192
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/112868
dc.language.isoen
dc.publisherPublic Library of Science
dc.relation.ispartofPLoS ONE
dc.relation.issn1932-6203
dc.relation.organizationDCD5A442BECFE17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc300 - Social sciences, sociology & anthropology::360 - Social problems & social services
dc.titleCopy number variation of the Beta-defensin genes in europeans: no supporting evidence for association with lung function, chronic obstructive pulmonary disease or asthma
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue1
oaire.citation.startPagee84192
oaire.citation.volume9
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
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unibe.date.licenseChanged2017-09-08 15:18:44
unibe.description.ispublishedpub
unibe.eprints.legacyId40721
unibe.journal.abbrevTitlePLOS ONE
unibe.refereedtrue
unibe.subtype.articlejournal

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