Cargando…

Asthma and genes encoding components of the vitamin D pathway

BACKGROUND: 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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bossé, Yohan, Lemire, Mathieu, Poon, Audrey H, Daley, Denise, He, Jian-Qing, Sandford, Andrew, White, John H, James, Alan L, Musk, Arthur William, Palmer, Lyle J, Raby, Benjamin A, Weiss, Scott T, Kozyrskyj, Anita L, Becker, Allan, Hudson, Thomas J, Laprise, Catherine
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779188/
https://www.ncbi.nlm.nih.gov/pubmed/19852851
http://dx.doi.org/10.1186/1465-9921-10-98
_version_ 1782174346766188544
author Bossé, Yohan
Lemire, Mathieu
Poon, Audrey H
Daley, Denise
He, Jian-Qing
Sandford, Andrew
White, John H
James, Alan L
Musk, Arthur William
Palmer, Lyle J
Raby, Benjamin A
Weiss, Scott T
Kozyrskyj, Anita L
Becker, Allan
Hudson, Thomas J
Laprise, Catherine
author_facet Bossé, Yohan
Lemire, Mathieu
Poon, Audrey H
Daley, Denise
He, Jian-Qing
Sandford, Andrew
White, John H
James, Alan L
Musk, Arthur William
Palmer, Lyle J
Raby, Benjamin A
Weiss, Scott T
Kozyrskyj, Anita L
Becker, Allan
Hudson, Thomas J
Laprise, Catherine
author_sort Bossé, Yohan
collection PubMed
description BACKGROUND: 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 < 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 < 0.0002). In the replicate samples, SNPs in the IL10 and CYP24A1 genes were again modestly associated with asthma and atopy (p < 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.
format Text
id pubmed-2779188
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-27791882009-11-19 Asthma and genes encoding components of the vitamin D pathway Bossé, Yohan Lemire, Mathieu Poon, Audrey H Daley, Denise He, Jian-Qing Sandford, Andrew White, John H James, Alan L Musk, Arthur William Palmer, Lyle J Raby, Benjamin A Weiss, Scott T Kozyrskyj, Anita L Becker, Allan Hudson, Thomas J Laprise, Catherine Respir Res Research BACKGROUND: 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 < 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 < 0.0002). In the replicate samples, SNPs in the IL10 and CYP24A1 genes were again modestly associated with asthma and atopy (p < 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. BioMed Central 2009 2009-10-24 /pmc/articles/PMC2779188/ /pubmed/19852851 http://dx.doi.org/10.1186/1465-9921-10-98 Text en Copyright ©2009 Bossé et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Bossé, Yohan
Lemire, Mathieu
Poon, Audrey H
Daley, Denise
He, Jian-Qing
Sandford, Andrew
White, John H
James, Alan L
Musk, Arthur William
Palmer, Lyle J
Raby, Benjamin A
Weiss, Scott T
Kozyrskyj, Anita L
Becker, Allan
Hudson, Thomas J
Laprise, Catherine
Asthma and genes encoding components of the vitamin D pathway
title Asthma and genes encoding components of the vitamin D pathway
title_full Asthma and genes encoding components of the vitamin D pathway
title_fullStr Asthma and genes encoding components of the vitamin D pathway
title_full_unstemmed Asthma and genes encoding components of the vitamin D pathway
title_short Asthma and genes encoding components of the vitamin D pathway
title_sort asthma and genes encoding components of the vitamin d pathway
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779188/
https://www.ncbi.nlm.nih.gov/pubmed/19852851
http://dx.doi.org/10.1186/1465-9921-10-98
work_keys_str_mv AT bosseyohan asthmaandgenesencodingcomponentsofthevitamindpathway
AT lemiremathieu asthmaandgenesencodingcomponentsofthevitamindpathway
AT poonaudreyh asthmaandgenesencodingcomponentsofthevitamindpathway
AT daleydenise asthmaandgenesencodingcomponentsofthevitamindpathway
AT hejianqing asthmaandgenesencodingcomponentsofthevitamindpathway
AT sandfordandrew asthmaandgenesencodingcomponentsofthevitamindpathway
AT whitejohnh asthmaandgenesencodingcomponentsofthevitamindpathway
AT jamesalanl asthmaandgenesencodingcomponentsofthevitamindpathway
AT muskarthurwilliam asthmaandgenesencodingcomponentsofthevitamindpathway
AT palmerlylej asthmaandgenesencodingcomponentsofthevitamindpathway
AT rabybenjamina asthmaandgenesencodingcomponentsofthevitamindpathway
AT weissscottt asthmaandgenesencodingcomponentsofthevitamindpathway
AT kozyrskyjanital asthmaandgenesencodingcomponentsofthevitamindpathway
AT beckerallan asthmaandgenesencodingcomponentsofthevitamindpathway
AT hudsonthomasj asthmaandgenesencodingcomponentsofthevitamindpathway
AT laprisecatherine asthmaandgenesencodingcomponentsofthevitamindpathway