Cargando…
A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan
Single nucleotide polymorphisms (SNPs) in the promoter region of CD209 (cluster of differentiation 209) may influence expression levels, and higher expression of CD209 on immune cells correlate with severity of cartilage destruction in patients with rheumatoid arthritis (RA). Due to the lack of a co...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128313/ https://www.ncbi.nlm.nih.gov/pubmed/33792986 http://dx.doi.org/10.1002/jcla.23751 |
_version_ | 1783694098491768832 |
---|---|
author | Chan, Hua‐Chen Wang, Shu‐Chen Lin, Chia‐Hui Lin, Yuan‐Zhao Li, Ruei‐Nian Yen, Jeng‐Hsien |
author_facet | Chan, Hua‐Chen Wang, Shu‐Chen Lin, Chia‐Hui Lin, Yuan‐Zhao Li, Ruei‐Nian Yen, Jeng‐Hsien |
author_sort | Chan, Hua‐Chen |
collection | PubMed |
description | Single nucleotide polymorphisms (SNPs) in the promoter region of CD209 (cluster of differentiation 209) may influence expression levels, and higher expression of CD209 on immune cells correlate with severity of cartilage destruction in patients with rheumatoid arthritis (RA). Due to the lack of a comprehensive study, this study aimed to investigate the CD209 promoter variants and haplotypes in a Taiwanese population and the association with RA development. Deoxyribonucleic acid (DNA) of peripheral blood mononuclear cells from 126 RA patients and 124 healthy controls was purified, and the CD209 gene promoter was amplified by polymerase chain reaction and analyzed by Sanger sequencing. Results showed that a novel variant −96C>A polymorphism in CD209 promoter was identified in the Taiwanese population, and the frequency was significantly higher in RA patients than in controls (11.51% vs. 2.42%, P < .0001). The odds ratio (OR) for the development of RA was 5.88 (95% CI 2.35–14.74, P < .0001). Other known variants were also evaluated; for instance, −1180 T/T (rs7359874) was increased in RA patients, and the OR for the development of RA was 3.26, 95% CI 0.85–12.52, P = .07). Besides, the haplotype frequencies were calculated; −1180A‐939C‐871 T‐336 T‐139 T‐96A and −1180 T‐939 T‐871C‐336 T‐139C‐96A were increased in RA patients (P = .004 and 0.05, respectively). In summary, CD209‐96A variant could be an important factor for the development of RA in the Taiwanese population. |
format | Online Article Text |
id | pubmed-8128313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81283132021-05-21 A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan Chan, Hua‐Chen Wang, Shu‐Chen Lin, Chia‐Hui Lin, Yuan‐Zhao Li, Ruei‐Nian Yen, Jeng‐Hsien J Clin Lab Anal Research Articles Single nucleotide polymorphisms (SNPs) in the promoter region of CD209 (cluster of differentiation 209) may influence expression levels, and higher expression of CD209 on immune cells correlate with severity of cartilage destruction in patients with rheumatoid arthritis (RA). Due to the lack of a comprehensive study, this study aimed to investigate the CD209 promoter variants and haplotypes in a Taiwanese population and the association with RA development. Deoxyribonucleic acid (DNA) of peripheral blood mononuclear cells from 126 RA patients and 124 healthy controls was purified, and the CD209 gene promoter was amplified by polymerase chain reaction and analyzed by Sanger sequencing. Results showed that a novel variant −96C>A polymorphism in CD209 promoter was identified in the Taiwanese population, and the frequency was significantly higher in RA patients than in controls (11.51% vs. 2.42%, P < .0001). The odds ratio (OR) for the development of RA was 5.88 (95% CI 2.35–14.74, P < .0001). Other known variants were also evaluated; for instance, −1180 T/T (rs7359874) was increased in RA patients, and the OR for the development of RA was 3.26, 95% CI 0.85–12.52, P = .07). Besides, the haplotype frequencies were calculated; −1180A‐939C‐871 T‐336 T‐139 T‐96A and −1180 T‐939 T‐871C‐336 T‐139C‐96A were increased in RA patients (P = .004 and 0.05, respectively). In summary, CD209‐96A variant could be an important factor for the development of RA in the Taiwanese population. John Wiley and Sons Inc. 2021-04-01 /pmc/articles/PMC8128313/ /pubmed/33792986 http://dx.doi.org/10.1002/jcla.23751 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Chan, Hua‐Chen Wang, Shu‐Chen Lin, Chia‐Hui Lin, Yuan‐Zhao Li, Ruei‐Nian Yen, Jeng‐Hsien A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan |
title | A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan |
title_full | A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan |
title_fullStr | A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan |
title_full_unstemmed | A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan |
title_short | A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan |
title_sort | novel cd209 polymorphism is associated with rheumatoid arthritis patients in taiwan |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128313/ https://www.ncbi.nlm.nih.gov/pubmed/33792986 http://dx.doi.org/10.1002/jcla.23751 |
work_keys_str_mv | AT chanhuachen anovelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT wangshuchen anovelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT linchiahui anovelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT linyuanzhao anovelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT lirueinian anovelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT yenjenghsien anovelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT chanhuachen novelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT wangshuchen novelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT linchiahui novelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT linyuanzhao novelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT lirueinian novelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan AT yenjenghsien novelcd209polymorphismisassociatedwithrheumatoidarthritispatientsintaiwan |