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The PTPN22 C1858T polymorphism and rheumatoid arthritis: a meta-analysis

Title
The PTPN22 C1858T polymorphism and rheumatoid arthritis: a meta-analysis
Author
배상철
Keywords
Protein tyrosine phosphatase nonreceptor 22; Polymorphism; Rheumatoid arthritis; Meta-analysis
Issue Date
2013-08
Publisher
Springer Science + Business Media
Citation
RHEUMATOLOGY INTERNATIONAL, Aug 2013, 33(8), P.1991-1999, 9P.
Abstract
The aim of this study was to determine whether the protein tyrosine phosphatase nonreceptor 22 (PTPN22) C1858T polymorphism confers susceptibility to rheumatoid arthritis (RA) in populations with different ethnicities. MEDLINE database and manual search were utilized to identify articles in which the PTPN22 polymorphism was determined in RA patients and controls. A meta-analysis was conducted on the associations between the PTPN22 C1858T polymorphism and RA using (1) allelic contrast and (2) dominant model. A total of 30 separate comparisons involving 17,961 RA patients and 18,611 controls were considered in this meta-analysis. Meta-analysis showed an association between the T allele and RA in all subjects (OR = 1.490, 95 % CI = 1.332-1.668, P < 1.0 x 10(-9)). After stratification by ethnicity, analysis indicated that the T allele was significantly associated with RA in Europeans and in Non-Europeans (OR = 1.423, 95 % CI = 1.260-1.605, P = 1.0 x 10(-8); OR = 1.902, 95 % CI = 1.488-2.430, P = 2.8 x 10(-8)). Meta-analysis of the CT + TT genotype showed the same result patterns as that shown by the PTPN22 C1858T polymorphism T allele. Furthermore, a direct comparison between rheumatoid factor (RF)-positive and RF-negative subjects revealed a significant association with the T allele in RA patients with RF, but not in subjects without RF (OR = 1.561, 95 % CI = 1.373-1.775, P < 1.0 x 10(-9)). This meta-analysis confirms that the PTPN22 C1858T polymorphism is associated with RA susceptibility in different ethnic groups, especially in Europeans, and the PTPN22 C1858T polymorphism T allele is significantly more prevalent in RF-positive patents than in RF-negative patients.
URI
https://link.springer.com/article/10.1007%2Fs00296-013-2679-2http://hdl.handle.net/20.500.11754/45477
ISSN
0172-8172
DOI
10.1007/s00296-013-2679-2
Appears in Collections:
COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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