The association between the PTPN22 C1858T polymorphism and rheumatoid arthritis

A meta-analysis update

Research output: Contribution to journalArticle

14 Citations (Scopus)

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. A meta-analysis was conducted on the PTPN22 C1858T polymorphism involving eighteen studies, which in total contained 20344 RA patients and 21828 controls. Metaanalysis revealed an association between the PTPN22 C1858T polymorphism T allele and RA in all subjects (odds ratio [OR] = 1.637, 95% confidence interval [CI] = 1.514-1.770, P<0.001). After stratification by ethnicity, analysis indicated that the PTPN22 C1858T polymorphism T allele was significantly associated with RA in Europeans and Non-Europeans (OR = 1.587, 95% CI = 1.486-1.696, P<0.001; OR = 1.748, 95% CI = 1.274-2.398, P< 0.001). 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 -negative subjects revealed a significant association with the T allele in RA patients with RF, but not in subjects without RF. In conclusion, 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.

Original languageEnglish
Pages (from-to)3453-3460
Number of pages8
JournalMolecular Biology Reports
Volume39
Issue number4
DOIs
Publication statusPublished - 2012 Apr 1

Fingerprint

Protein Tyrosine Phosphatases
Meta-Analysis
Rheumatoid Arthritis
Rheumatoid Factor
Alleles
Odds Ratio
Confidence Intervals
Patents
Ethnic Groups
Genotype
Population

Keywords

  • Meta-analysis
  • Polymorphism
  • Protein tyrosine phosphatase nonreceptor 22
  • Rheumatoid arthritis

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics

Cite this

@article{7ac9eca1a9624a06bf7c2db961a8d1ac,
title = "The association between the PTPN22 C1858T polymorphism and rheumatoid arthritis: A meta-analysis update",
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. A meta-analysis was conducted on the PTPN22 C1858T polymorphism involving eighteen studies, which in total contained 20344 RA patients and 21828 controls. Metaanalysis revealed an association between the PTPN22 C1858T polymorphism T allele and RA in all subjects (odds ratio [OR] = 1.637, 95{\%} confidence interval [CI] = 1.514-1.770, P<0.001). After stratification by ethnicity, analysis indicated that the PTPN22 C1858T polymorphism T allele was significantly associated with RA in Europeans and Non-Europeans (OR = 1.587, 95{\%} CI = 1.486-1.696, P<0.001; OR = 1.748, 95{\%} CI = 1.274-2.398, P< 0.001). 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 -negative subjects revealed a significant association with the T allele in RA patients with RF, but not in subjects without RF. In conclusion, 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.",
keywords = "Meta-analysis, Polymorphism, Protein tyrosine phosphatase nonreceptor 22, Rheumatoid arthritis",
author = "Lee, {Young Ho} and Bae, {Sang Cheol} and Sungjae Choi and Ji, {Jong Dae} and Song, {Gwan Gyu}",
year = "2012",
month = "4",
day = "1",
doi = "10.1007/s11033-011-1117-3",
language = "English",
volume = "39",
pages = "3453--3460",
journal = "Molecular Biology Reports",
issn = "0301-4851",
publisher = "Springer Netherlands",
number = "4",

}

TY - JOUR

T1 - The association between the PTPN22 C1858T polymorphism and rheumatoid arthritis

T2 - A meta-analysis update

AU - Lee, Young Ho

AU - Bae, Sang Cheol

AU - Choi, Sungjae

AU - Ji, Jong Dae

AU - Song, Gwan Gyu

PY - 2012/4/1

Y1 - 2012/4/1

N2 - 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. A meta-analysis was conducted on the PTPN22 C1858T polymorphism involving eighteen studies, which in total contained 20344 RA patients and 21828 controls. Metaanalysis revealed an association between the PTPN22 C1858T polymorphism T allele and RA in all subjects (odds ratio [OR] = 1.637, 95% confidence interval [CI] = 1.514-1.770, P<0.001). After stratification by ethnicity, analysis indicated that the PTPN22 C1858T polymorphism T allele was significantly associated with RA in Europeans and Non-Europeans (OR = 1.587, 95% CI = 1.486-1.696, P<0.001; OR = 1.748, 95% CI = 1.274-2.398, P< 0.001). 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 -negative subjects revealed a significant association with the T allele in RA patients with RF, but not in subjects without RF. In conclusion, 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.

AB - 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. A meta-analysis was conducted on the PTPN22 C1858T polymorphism involving eighteen studies, which in total contained 20344 RA patients and 21828 controls. Metaanalysis revealed an association between the PTPN22 C1858T polymorphism T allele and RA in all subjects (odds ratio [OR] = 1.637, 95% confidence interval [CI] = 1.514-1.770, P<0.001). After stratification by ethnicity, analysis indicated that the PTPN22 C1858T polymorphism T allele was significantly associated with RA in Europeans and Non-Europeans (OR = 1.587, 95% CI = 1.486-1.696, P<0.001; OR = 1.748, 95% CI = 1.274-2.398, P< 0.001). 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 -negative subjects revealed a significant association with the T allele in RA patients with RF, but not in subjects without RF. In conclusion, 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.

KW - Meta-analysis

KW - Polymorphism

KW - Protein tyrosine phosphatase nonreceptor 22

KW - Rheumatoid arthritis

UR - http://www.scopus.com/inward/record.url?scp=84862992023&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84862992023&partnerID=8YFLogxK

U2 - 10.1007/s11033-011-1117-3

DO - 10.1007/s11033-011-1117-3

M3 - Article

VL - 39

SP - 3453

EP - 3460

JO - Molecular Biology Reports

JF - Molecular Biology Reports

SN - 0301-4851

IS - 4

ER -