Ramírez-Pérez S, Sánchez-Zuno G A, Chavarría-Buenrostro L E, Montoya-Buelna M, Reyes-Pérez I V, Ramírez-Dueñas M G, Palafox-Sánchez C A, Martínez-Bonilla G E, Muñoz-Valle J F
Research Institute in Biomedical Sciences, University Center of Health Science, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Transdisciplinary Institute of Research and Services (ITRANS), University of Guadalajara, Zapopan, Jalisco, Mexico.
Biochem Genet. 2019 Jun;57(3):455-465. doi: 10.1007/s10528-019-09902-8. Epub 2019 Jan 14.
PTPN22 represents an important non-HLA gene that has been strongly associated with rheumatoid arthritis (RA) pathogenesis. Several studies have reported a specific genetic variant for PTPN22 (+788 G>A; rs33996649) that might be associated with decreased RA risk in Caucasian population; nevertheless, its specific role in western Mexican population has not been yet described. A case-control study with 443 RA patients and 317 control subjects (CS) was conducted. The genotyping was performed by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) technique and the PTPN22 mRNA expression was determined by SYBR Green-based real-time quantitative-PCR assay. No association between the PTPN22 +788 G>A polymorphism and RA susceptibility in western Mexican population was found when comparing genotype and allelic frequencies between RA patients and CS (G/G vs. G/A: OR 0.55, p = 0.14, 95% CI 0.22-1.32; G vs. A: OR 0.56, p = 0.14, 95% CI 0.23-1.36). The PTPN22 mRNA expression increased 4.6-fold more in RA patients than in CS, and RA patients, carriers of PTPN22 +788 G/A genotype, expressed 15.6-fold more than RA patients carrying the homozygous G/G genotype. Overall, these results showed that the PTPN22 +788 G>A polymorphism is not associated with RA susceptibility in western Mexican population, whereas the presence of G/A genotype is associated with increased PTPN22 mRNA expression in RA patients.
蛋白酪氨酸磷酸酶非受体型22(PTPN22)是一种重要的非人类白细胞抗原(HLA)基因,与类风湿关节炎(RA)的发病机制密切相关。多项研究报道了PTPN22的一种特定基因变异(+788 G>A;rs33996649),该变异可能与白种人群中RA风险降低有关;然而,其在墨西哥西部人群中的具体作用尚未见报道。我们开展了一项病例对照研究,纳入443例RA患者和317例对照受试者(CS)。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术进行基因分型,并通过基于SYBR Green的实时定量PCR检测法测定PTPN22 mRNA表达。比较RA患者和CS的基因型及等位基因频率时,未发现墨西哥西部人群中PTPN22 +788 G>A多态性与RA易感性之间存在关联(G/G与G/A比较:比值比[OR]为0.55,p = 0.14,95%置信区间[CI]为0.22 - 1.32;G与A比较:OR为0.56,p = 0.14,95% CI为0.23 - 1.36)。RA患者的PTPN22 mRNA表达比CS增加了4.6倍,携带PTPN22 +788 G/A基因型的RA患者表达量比携带纯合G/G基因型的RA患者高15.6倍。总体而言,这些结果表明,PTPN22 +788 G>A多态性与墨西哥西部人群的RA易感性无关,而G/A基因型的存在与RA患者中PTPN22 mRNA表达增加有关。