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Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population
OBJECTIVE: Type 1 diabetes (T1D) and rheumatoid arthritis (RA) are autoimmune diseases. It is known that certain genetic loci and factors that increase the overall autoimmunity risk can be shared among different autoimmune diseases. We sought to replicate seven T1D-related SNPs (single nucleotide po...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712654/ https://www.ncbi.nlm.nih.gov/pubmed/31455420 http://dx.doi.org/10.1186/s13104-019-4590-8 |
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author | Aslam, Muhammad Muaaz John, Peter Fan, Kang-Hsien Bhatti, Attya Jahangir, Sidrah Feingold, Eleanor Demirci, F. Yesim Kamboh, M. Ilyas |
author_facet | Aslam, Muhammad Muaaz John, Peter Fan, Kang-Hsien Bhatti, Attya Jahangir, Sidrah Feingold, Eleanor Demirci, F. Yesim Kamboh, M. Ilyas |
author_sort | Aslam, Muhammad Muaaz |
collection | PubMed |
description | OBJECTIVE: Type 1 diabetes (T1D) and rheumatoid arthritis (RA) are autoimmune diseases. It is known that certain genetic loci and factors that increase the overall autoimmunity risk can be shared among different autoimmune diseases. We sought to replicate seven T1D-related SNPs (single nucleotide polymorphisms) that have been previously reported to be associated with RA susceptibility in a small set of mixed family-based and case–control Pakistani sample in a relatively large and independent RA case–control sample from the same population. Seven T1D-associated SNPs (GLIS3/rs7020673, BACH2/rs11755527, SKAP2/rs7804356, GDSMB/rs2290400, C6orf173/rs9388489, LOC399716/rs947474 and DLK1-MEG2/rs941576) were genotyped in a large Pakistani RA case–control sample (n = 1959) using TaqMan(®) SNP genotyping assays. RESULTS: None of the tested SNPs showed statistically significant association with RA susceptibility; however, one SNP (GLIS3/rs7020673) showed a trend for association (OR = 0.88, p = 7.99E−02). Our study has failed to replicate the previously reported association of seven T1D-associated SNPs with RA risk in a large sample from the same population. Thus, our results do not support a major role of these T1D SNPs in affecting RA susceptibility in the Pakistani population. |
format | Online Article Text |
id | pubmed-6712654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67126542019-08-29 Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population Aslam, Muhammad Muaaz John, Peter Fan, Kang-Hsien Bhatti, Attya Jahangir, Sidrah Feingold, Eleanor Demirci, F. Yesim Kamboh, M. Ilyas BMC Res Notes Research Note OBJECTIVE: Type 1 diabetes (T1D) and rheumatoid arthritis (RA) are autoimmune diseases. It is known that certain genetic loci and factors that increase the overall autoimmunity risk can be shared among different autoimmune diseases. We sought to replicate seven T1D-related SNPs (single nucleotide polymorphisms) that have been previously reported to be associated with RA susceptibility in a small set of mixed family-based and case–control Pakistani sample in a relatively large and independent RA case–control sample from the same population. Seven T1D-associated SNPs (GLIS3/rs7020673, BACH2/rs11755527, SKAP2/rs7804356, GDSMB/rs2290400, C6orf173/rs9388489, LOC399716/rs947474 and DLK1-MEG2/rs941576) were genotyped in a large Pakistani RA case–control sample (n = 1959) using TaqMan(®) SNP genotyping assays. RESULTS: None of the tested SNPs showed statistically significant association with RA susceptibility; however, one SNP (GLIS3/rs7020673) showed a trend for association (OR = 0.88, p = 7.99E−02). Our study has failed to replicate the previously reported association of seven T1D-associated SNPs with RA risk in a large sample from the same population. Thus, our results do not support a major role of these T1D SNPs in affecting RA susceptibility in the Pakistani population. BioMed Central 2019-08-27 /pmc/articles/PMC6712654/ /pubmed/31455420 http://dx.doi.org/10.1186/s13104-019-4590-8 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Note Aslam, Muhammad Muaaz John, Peter Fan, Kang-Hsien Bhatti, Attya Jahangir, Sidrah Feingold, Eleanor Demirci, F. Yesim Kamboh, M. Ilyas Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population |
title | Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population |
title_full | Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population |
title_fullStr | Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population |
title_full_unstemmed | Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population |
title_short | Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population |
title_sort | exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the pakistani population |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712654/ https://www.ncbi.nlm.nih.gov/pubmed/31455420 http://dx.doi.org/10.1186/s13104-019-4590-8 |
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