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...

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Main Authors: Ostanek, Lidia, Ostanek-Pańka, Magdalena, Bobrowska-Snarska, Danuta, Bińczak-Kuleta, Agnieszka, Fischer, Katarzyna, Kaczmarczyk, Mariusz, Ciechanowicz, Andrzej, Brzosko, Marek
Format: Online
Language:English
Published: Springer Netherlands 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141968/
id pubmed-4141968
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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/
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