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Association of the PTPN22 gene (-1123G > C) polymorphism with rheumatoid arthritis in Chinese patients
18
Citations
14
References
2010
Year
Single Nucleotide PolymorphismGeneticsGenetic EpidemiologyImmunologyHuman PolymorphismImmune-related Gene PolymorphismRheumatoid DisorderDisease SusceptibilityInflammatory Rheumatic DiseasePublic HealthRheumatoid ArthritisRheumatologyAutoimmune DiseaseRheumatic DiseasesStatistical GeneticsAutoimmunityPtpn22 GeneEpidemiologyMedicineChinese Patients
This study aimed at examining the association of the single nucleotide polymorphism (SNP) in the protein tyrosine phosphatase gene (PTPN22) with the risk of rheumatoid arthritis (RA) in a Chinese population. A total of 200 RA patients and age and gender-matched healthy controls were recruited. Their genotypes and allelic frequency were determined by the TaqMan-MGB probe-based polymerase chain reaction (PCR). The frequencies of the CC genotype and C allele in RA patient group were significantly higher than that of controls (P < 0.01 or P < 0.05) with an odds ratio of 1.67, respectively. These data suggest, the CC genotype and C allele of the -1123G > C in the PTPN22 gene are associated with an increased risk for RA in Chinese population. Therefore, the CC genotype and C allele of the -1123G > C in the PTPN22 gene may be used as a genetic marker for the predisposition of RA in Chinese.
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