PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical results
To assess the association between PTPN22 1858C>T gene polymorphism and susceptibility to, and clinical presentation of, systemic lupus erythematosus (SLE). Our study included 135 SLE patients (120 women and 15 men; mean age 45.1 years; mean course of disease from 0.5 to 31 years) and 201 healthy...
Main Authors: | , , , , , , , |
---|---|
Format: | Online |
Language: | English |
Published: |
Springer Netherlands
2014
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141968/ |
id |
pubmed-4141968 |
---|---|
recordtype |
oai_dc |
spelling |
pubmed-41419682014-08-25 PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical results Ostanek, Lidia Ostanek-Pańka, Magdalena Bobrowska-Snarska, Danuta Bińczak-Kuleta, Agnieszka Fischer, Katarzyna Kaczmarczyk, Mariusz Ciechanowicz, Andrzej Brzosko, Marek Article To assess the association between PTPN22 1858C>T gene polymorphism and susceptibility to, and clinical presentation of, systemic lupus erythematosus (SLE). Our study included 135 SLE patients (120 women and 15 men; mean age 45.1 years; mean course of disease from 0.5 to 31 years) and 201 healthy subjects. The PTPN22 1858C>T gene polymorphism was genotyped by polymerase chain reaction restriction fragment length polymorphism. A significantly higher incidence of genotype CT in patients with SLE (36.3 %) was found, compared with the control group (24.9 %). The frequencies of C1858 and T1858 alleles were 78.1 and 21.9 % in SLE patients and 86.1 and 13.9 % in controls, respectively. Significantly higher SLE susceptibility was observed in patients carrying at least one T allele (p = 0.009; OR 1.86; 95 % CI 0.14–3.05). Significant association of the PTPN22 T1858 allele (CT + TT vs.CC) and secondary antiphospholipid syndrome was observed (p = 0.049). In SLE patients carrying the T1858 allele, higher levels of antiphospholipid antibodies (anticardiolipin antibodies and/or lupus anticoagulant) were found (p = 0.030; OR 2.17; 95 % CI 1.07–4.44). Springer Netherlands 2014-07-02 2014 /pmc/articles/PMC4141968/ /pubmed/24985973 http://dx.doi.org/10.1007/s11033-014-3498-6 Text en © The Author(s) 2014 Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Ostanek, Lidia Ostanek-Pańka, Magdalena Bobrowska-Snarska, Danuta Bińczak-Kuleta, Agnieszka Fischer, Katarzyna Kaczmarczyk, Mariusz Ciechanowicz, Andrzej Brzosko, Marek |
spellingShingle |
Ostanek, Lidia Ostanek-Pańka, Magdalena Bobrowska-Snarska, Danuta Bińczak-Kuleta, Agnieszka Fischer, Katarzyna Kaczmarczyk, Mariusz Ciechanowicz, Andrzej Brzosko, Marek PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical results |
author_facet |
Ostanek, Lidia Ostanek-Pańka, Magdalena Bobrowska-Snarska, Danuta Bińczak-Kuleta, Agnieszka Fischer, Katarzyna Kaczmarczyk, Mariusz Ciechanowicz, Andrzej Brzosko, Marek |
author_sort |
Ostanek, Lidia |
title |
PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical results |
title_short |
PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical results |
title_full |
PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical results |
title_fullStr |
PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical results |
title_full_unstemmed |
PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical results |
title_sort |
ptpn22 1858c>t gene polymorphism in patients with sle: association with serological and clinical results |
description |
To assess the association between PTPN22 1858C>T gene polymorphism and susceptibility to, and clinical presentation of, systemic lupus erythematosus (SLE). Our study included 135 SLE patients (120 women and 15 men; mean age 45.1 years; mean course of disease from 0.5 to 31 years) and 201 healthy subjects. The PTPN22 1858C>T gene polymorphism was genotyped by polymerase chain reaction restriction fragment length polymorphism. A significantly higher incidence of genotype CT in patients with SLE (36.3 %) was found, compared with the control group (24.9 %). The frequencies of C1858 and T1858 alleles were 78.1 and 21.9 % in SLE patients and 86.1 and 13.9 % in controls, respectively. Significantly higher SLE susceptibility was observed in patients carrying at least one T allele (p = 0.009; OR 1.86; 95 % CI 0.14–3.05). Significant association of the PTPN22 T1858 allele (CT + TT vs.CC) and secondary antiphospholipid syndrome was observed (p = 0.049). In SLE patients carrying the T1858 allele, higher levels of antiphospholipid antibodies (anticardiolipin antibodies and/or lupus anticoagulant) were found (p = 0.030; OR 2.17; 95 % CI 1.07–4.44). |
publisher |
Springer Netherlands |
publishDate |
2014 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141968/ |
_version_ |
1613126871496523776 |