Liu Yalong, Chaudhary Ayesha, Quddus Kanza, Aslam Mehwish, Iftikhar Anisa, Khan Azmat Ali, Alanazi Amer M, Bashir Kashif
Orthopedics Department 3, Heilongjiang Beidahuang Group General Hospital, Harbin City, Heilongjiang Province, China.
Department of Zoology, University of Sargodha, Sargodha, Pakistan.
Int J Immunogenet. 2025 Oct;52(5):262-273. doi: 10.1111/iji.70007. Epub 2025 Jul 22.
The main objective of the study was to determine the association of genes AIRE (rs2075876), CD40 (rs4810485), HLA-DRB1 (rs6457617) and TRAF1/C5 (rs10818488) polymorphisms with rheumatoid arthritis (RA) from the population of Pakistan. Blood samples of 300 RA patients and 300 healthy controls were taken from different hospitals in Pakistan. Extraction of DNA was carried out; a specific region of DNA was amplified using PCR. Polymorphic analysis was performed for genes AIRE (rs2075876), CD40 (rs4810485), HLA-DRB1 (rs6457617) and TRAF1/C5 (rs10818488). The demographic parameters, like age, showed statistically significant association and increased the risk of the disease up to 2-fold (odds ratio [OR] = 2.57; 95% confidence interval [CI] = 1.60-4.12; p = 0.0001). Gender and family history did not show any significant association with arthritis (OR = 1.12; 95% CI = 0.69-1.81; p = 0.6260; OR = 0.70; 95% CI = 0.44-1.11; p = 0.1313, respectively). In the case of smoking status, the difference was statistically significant for both smokers and non-smokers. In smokers, there was a decreased risk of RA (OR = 0.45; 95% CI = 0.28-0.73; p = 0.0011), and in non-smokers, there was an increased risk of disease up to 2-fold (OR = 2.17; 95% CI = 1.36-3.47; p = 0.0011). In AIRE gene, heterozygous (AG) of rs2075876 showed a highly significant association with increased risk of RA up to 3-fold (OR = 3.39; 95% CI = 2.08-5.54; p = 0.0001), whereas homozygous mutant (GG) also showed significant association (OR = 0.43; 95% CI = 0.26-0.72; p = 0.0014) but with decreased risk. In CD40 gene, heterozygous (AG) of rs4810485 showed significant association with a decreased risk of RA (OR = 0.59; 95% CI = 0.377-0.945; p = 0.027), whereas the homozygous mutant (GG) of rs4810485 showed highly significant association by increasing risk of up to 4-fold (OR = 4.318; 95% CI = 2.553-7.303; p = 0.0001). In HLA-DRB1 gene, heterozygous (CT) of rs6457617 showed significant association with a decreased risk of disease (OR = 0.52; 95% CI = 0.35-0.85; p = 0.007), whereas the homozygous mutant (TT) of rs6457617 showed highly significant association by increasing the risk of RA up to 4-fold (OR = 4.37; 95% CI = 2.55-7.47; p = 0.0001). In the TRAF1/C5 gene, heterozygosity (AG) of rs10818488 showed a significant association with an increased risk of disease up to 4-fold (OR = 4.06; 95% CI = 2.38-6.98; p = 0.0001). Highly significant associations of genes AIRE (rs2075876), CD40 (rs4810485), HLA-DRB1 (rs6457617) and TRAF1/C5 (rs10818488) polymorphisms were observed with RA.
该研究的主要目的是确定来自巴基斯坦人群的AIRE(rs2075876)、CD40(rs4810485)、HLA - DRB1(rs6457617)和TRAF1/C5(rs10818488)基因多态性与类风湿性关节炎(RA)之间的关联。从巴基斯坦不同医院采集了300例RA患者和300例健康对照的血样。进行了DNA提取;使用聚合酶链反应(PCR)扩增DNA的特定区域。对AIRE(rs2075876)、CD40(rs4810485)、HLA - DRB1(rs6457617)和TRAF1/C5(rs10818488)基因进行了多态性分析。年龄等人口统计学参数显示出具有统计学意义的关联,并且使疾病风险增加了2倍(优势比[OR]=2.57;95%置信区间[CI]=1.60 - 4.12;p = 0.0001)。性别和家族史与关节炎未显示出任何显著关联(OR分别为1.12;95% CI = 0.69 - 1.81;p = 0.6260;OR为0.70;95% CI = 0.44 - 1.11;p = 0.1313)。在吸烟状况方面,吸烟者和非吸烟者之间的差异具有统计学意义。吸烟者患RA的风险降低(OR = 0.45;95% CI = 0.28 - 0.73;p = 0.0011),而非吸烟者患疾病的风险增加了2倍(OR = 2.17;95% CI = 1.36 - 3.47;p = 0.0011)。在AIRE基因中,rs2075876的杂合子(AG)与RA风险增加高达3倍显示出高度显著关联(OR = 3.39;95% CI = 2.08 - 5.54;p = 0.0001),而纯合突变体(GG)也显示出显著关联(OR = 0.43;95% CI = 0.26 - 0.72;p = 0.0014),但风险降低。在CD40基因中,rs4810485的杂合子(AG)与RA风险降低显示出显著关联(OR = 0.59;95% CI = 0.377 - 0.945;p = 0.027),而rs4810485的纯合突变体(GG)通过使风险增加高达4倍显示出高度显著关联(OR = 4.318;95% CI = 2.553 - 7.303;p = 0.0001)。在HLA - DRB1基因中,rs6457617的杂合子(CT)与疾病风险降低显示出显著关联(OR = 0.52;95% CI = 0.35 - 0.85;p = 0.007),而rs6457617的纯合突变体(TT)通过使RA风险增加高达4倍显示出高度显著关联(OR = 4.37;95% CI = 2.55 - 7.47;p = 0.0001)。在TRAF1/C5基因中,rs10818488的杂合性(AG)与疾病风险增加高达4倍显示出显著关联(OR = 4.06;95% CI = 2.38 - 6.98;p = 0.0001)。观察到AIRE(rs2075876)、CD40(rs4810485)、HLA - DRB1(rs6457617)和TRAF1/C5(rs10818488)基因多态性与RA之间存在高度显著关联。