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dc.contributor.authorBossé, Yohan
dc.contributor.authorLemire, Mathieu
dc.contributor.authorPoon, Audrey H
dc.contributor.authorDaley, Denise
dc.contributor.authorHe, Jian-Qing
dc.contributor.authorSandford, Andrew
dc.contributor.authorJames, Alan L
dc.contributor.authorMusk, Arthur William
dc.contributor.authorPalmer, Lyle J
dc.contributor.authorKozyrskyj, Anita L
dc.contributor.authorBecker, Allan
dc.contributor.authorHudson, Thomas J
dc.contributor.authorLaprise, Catherine
dc.contributor.authorWhite, John H.
dc.contributor.authorRaby, Benjamin Alexander
dc.contributor.authorWeiss, Scott Tillman
dc.date.accessioned2012-01-05T04:59:55Z
dc.date.issued2009
dc.identifier.citationBosse, Yohan, Mathieu Lemire, Audrey H. Poon, Denise Daley, Jian-Qing He, Andrew Sandford, John H. White, et al. 2009. Asthma and genes encoding components of the vitamin D pathway. Respiratory Research 10(1): 98.en_US
dc.identifier.issn1465-9921en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:6530694
dc.description.abstractBackground: Genetic variants at the vitamin D receptor (VDR) locus are associated with asthma and atopy. We hypothesized that polymorphisms in other genes of the vitamin D pathway are associated with asthma or atopy. Methods: Eleven candidate genes were chosen for this study, five of which code for proteins in the vitamin D metabolism pathway (CYP27A1, CYP27B1, CYP2R1, CYP24A1, GC) and six that are known to be transcriptionally regulated by vitamin D (IL10, IL1RL1, CD28, CD86, IL8, SKIIP). For each gene, we selected a maximally informative set of common SNPs (tagSNPs) using the European-derived (CEU) HapMap dataset. A total of 87 SNPs were genotyped in a French-Canadian family sample ascertained through asthmatic probands (388 nuclear families, 1064 individuals) and evaluated using the Family Based Association Test (FBAT) program. We then sought to replicate the positive findings in four independent samples: two from Western Canada, one from Australia and one from the USA (CAMP). Results: A number of SNPs in the IL10, CYP24A1, CYP2R1, IL1RL1 and CD86 genes were modestly associated with asthma and atopy (p less than 0.05). Two-gene models testing for both main effects and the interaction were then performed using conditional logistic regression. Two-gene models implicating functional variants in the IL10 and VDR genes as well as in the IL10 and IL1RL1 genes were associated with asthma (p less than 0.0002). In the replicate samples, SNPs in the IL10 and CYP24A1 genes were again modestly associated with asthma and atopy (p less than 0.05). However, the SNPs or the orientation of the risk alleles were different between populations. A two-gene model involving IL10 and VDR was replicated in CAMP, but not in the other populations. Conclusion: A number of genes involved in the vitamin D pathway demonstrate modest levels of association with asthma and atopy. Multilocus models testing genes in the same pathway are potentially more effective to evaluate the risk of asthma, but the effects are not uniform across populations.en_US
dc.language.isoen_USen_US
dc.publisherBioMed Centralen_US
dc.relation.isversionofdoi:10.1186/1465-9921-10-98en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779188/pdf/en_US
dash.licenseLAA
dc.titleAsthma and Genes Encoding Components of the Vitamin D Pathwayen_US
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden_US
dc.relation.journalRespiratory Researchen_US
dash.depositing.authorRaby, Benjamin Alexander
dc.date.available2012-01-05T04:59:55Z
dash.affiliation.otherHMS^Medicine-Brigham and Women's Hospitalen_US
dash.affiliation.otherHMS^Medicine-Brigham and Women's Hospitalen_US
dash.affiliation.otherSPH^Molecular+Integrative Physiological Sci Progen_US
dc.identifier.doi10.1186/1465-9921-10-98*
dash.authorsorderedfalse
dash.contributor.affiliatedRaby, Benjamin
dash.contributor.affiliatedWeiss, Scott


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