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Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis

BACKGROUND: There is strong evidence suggesting that juvenile idiopathic arthritis (JIA) shares many susceptibility loci with other autoimmune diseases. OBJECTIVE: To investigate variants robustly associated with type 1 diabetes (T1D) or coeliac disease (CD) for association with JIA. METHODS: Sixtee...

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Autores principales: Hinks, Anne, Martin, Paul, Flynn, Edward, Eyre, Steve, Packham, Jon, Barton, Anne, Worthington, Jane, Thomson, Wendy
Formato: Texto
Lenguaje:English
Publicado: BMJ Group 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002762/
https://www.ncbi.nlm.nih.gov/pubmed/20647273
http://dx.doi.org/10.1136/ard.2009.126938
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author Hinks, Anne
Martin, Paul
Flynn, Edward
Eyre, Steve
Packham, Jon
Barton, Anne
Worthington, Jane
Thomson, Wendy
author_facet Hinks, Anne
Martin, Paul
Flynn, Edward
Eyre, Steve
Packham, Jon
Barton, Anne
Worthington, Jane
Thomson, Wendy
author_sort Hinks, Anne
collection PubMed
description BACKGROUND: There is strong evidence suggesting that juvenile idiopathic arthritis (JIA) shares many susceptibility loci with other autoimmune diseases. OBJECTIVE: To investigate variants robustly associated with type 1 diabetes (T1D) or coeliac disease (CD) for association with JIA. METHODS: Sixteen single-nucleotide polymorphisms (SNPs) already identified as susceptibility loci for T1D/CD were selected for genotyping in patients with JIA (n=1054) and healthy controls (n=3129). Genotype and allele frequencies were compared using the Cochrane–Armitage trend test implemented in PLINK. RESULTS: One SNP in the LPP gene, rs1464510, showed significant association with JIA (p(trend)=0.002, OR=1.18, 95% CI 1.06 to 1.30). A second SNP, rs653178 in ATXN2, also showed nominal evidence for association with JIA (p(trend)=0.02, OR=1.13, 95% CI 1.02 to 1.25). The SNP, rs17810546, in IL12A showed subtype-specific association with enthesitis-related arthritis (ERA) subtype (p(trend)=0.005, OR=1.88, 95% CI 1.2 to 2.94). CONCLUSIONS: Evidence for a novel JIA susceptibility locus, LPP, is presented. Association at the SH2B3/ATXN2 locus, previously reported to be associated with JIA in a US series, also supports this region as contributing to JIA susceptibility. In addition, a subtype-specific association of IL12A with ERA is identified. All findings will require validation in independent JIA cohorts.
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spelling pubmed-30027622011-01-03 Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis Hinks, Anne Martin, Paul Flynn, Edward Eyre, Steve Packham, Jon Barton, Anne Worthington, Jane Thomson, Wendy Ann Rheum Dis Clinical and Epidemiological Research BACKGROUND: There is strong evidence suggesting that juvenile idiopathic arthritis (JIA) shares many susceptibility loci with other autoimmune diseases. OBJECTIVE: To investigate variants robustly associated with type 1 diabetes (T1D) or coeliac disease (CD) for association with JIA. METHODS: Sixteen single-nucleotide polymorphisms (SNPs) already identified as susceptibility loci for T1D/CD were selected for genotyping in patients with JIA (n=1054) and healthy controls (n=3129). Genotype and allele frequencies were compared using the Cochrane–Armitage trend test implemented in PLINK. RESULTS: One SNP in the LPP gene, rs1464510, showed significant association with JIA (p(trend)=0.002, OR=1.18, 95% CI 1.06 to 1.30). A second SNP, rs653178 in ATXN2, also showed nominal evidence for association with JIA (p(trend)=0.02, OR=1.13, 95% CI 1.02 to 1.25). The SNP, rs17810546, in IL12A showed subtype-specific association with enthesitis-related arthritis (ERA) subtype (p(trend)=0.005, OR=1.88, 95% CI 1.2 to 2.94). CONCLUSIONS: Evidence for a novel JIA susceptibility locus, LPP, is presented. Association at the SH2B3/ATXN2 locus, previously reported to be associated with JIA in a US series, also supports this region as contributing to JIA susceptibility. In addition, a subtype-specific association of IL12A with ERA is identified. All findings will require validation in independent JIA cohorts. BMJ Group 2010-07-20 /pmc/articles/PMC3002762/ /pubmed/20647273 http://dx.doi.org/10.1136/ard.2009.126938 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Clinical and Epidemiological Research
Hinks, Anne
Martin, Paul
Flynn, Edward
Eyre, Steve
Packham, Jon
Barton, Anne
Worthington, Jane
Thomson, Wendy
Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis
title Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis
title_full Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis
title_fullStr Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis
title_full_unstemmed Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis
title_short Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis
title_sort investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis
topic Clinical and Epidemiological Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002762/
https://www.ncbi.nlm.nih.gov/pubmed/20647273
http://dx.doi.org/10.1136/ard.2009.126938
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