Protein tyrosine phosphatase gene C1858T allele confers risk for rheumatoid arthritis in Hungarian subjects

被引:0
作者
Bernadett Farago
Gabor C. Talian
Katalin Komlosi
Gergely Nagy
Timea Berki
Agnes Gyetvai
Zoltan Szekanecz
Zoltan Nyarady
Csaba G. Kiss
Peter Nemeth
Laszlo Czirjak
Bela Melegh
机构
[1] University of Pécs,Department of Medical Genetics and Child Development
[2] University of Pécs,Department of Forensic Medicine
[3] University of Pécs,Department of Immunology and Biotechnology
[4] University of Debrecen Medical and Health Science Center,Laboratory of Immunology, 3rd Department of Internal Medicine
[5] University of Debrecen Medical and Health Science Center,Division of Rheumatology, 3rd Department of Internal Medicine
[6] University of Pécs,Department of Oral and Maxillofacial Surgery
[7] University of Pécs,Department of Immunology and Rheumatology
来源
Rheumatology International | 2009年 / 29卷
关键词
PTPN22; Rheumatoid arthritis; Polymorphism; RF; Anti-CCP;
D O I
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中图分类号
学科分类号
摘要
The C1858T allele of the PTPN22 gene has been reported to confer risk for RA; but in some reports, the effect was restricted to RF- and/or anti-CCP-seropositive patients. Hungarian RA patients and matched controls were genotyped. The 1858T allele showed an increased prevalence in RA patients compared to controls. The 1858T allele represents a risk factor in the whole RA population (P = 0.001); an association was found both in RF-seropositive (P = 0.001) and anti-CCP-seropositive patients (P = 0.001), and in subjects with the combination of these factors (P = 0.002). In TT homozygotes, the estimated susceptibility to RA was more than double (OR = 5.04) of that seen in TC heterozygotes (OR = 1.89); the same gene dosage effect was observed in all seropositive RA subgroups. Our data show that the Hungarian RA patients belong to the populations in which the 1858T allele represents a susceptibility factor both in the RF- and/or anti-CCP-seropositive subjects, and the association exhibit a gene dosage dependency.
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页码:793 / 796
页数:3
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