Wu Ye, Chen Yuting, Sun Xiaoya, Deng Yujie, Ni Man, Pan Faming
Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, 81 Meishan Road, Hefei, 230032, Anhui, China.
The Key Laboratory of Major Autoimmune Diseases, Anhui Medical University, 81 Meishan Road, Hefei, 230032, Anhui, China.
Genes Immun. 2023 Feb;24(1):46-51. doi: 10.1038/s41435-023-00196-w. Epub 2023 Jan 27.
Ankylosing spondylitis (AS) is an autoimmune-related inflammatory arthritis. The association between the DNA methylation and mRNA expression of PDCD1 gene with the susceptibility to AS remains unclear. In this case-control study, the methylation level of PDCD1 promoter was detected in 80 AS patients and 80 healthy controls by MethylTarget method. The transcriptional level of PDCD1 gene was measured in 47 AS patients and 47 healthy controls by real-time quantitative PCR. Finally, 17 methylation sites mapped to one CpG island were detected. Compared to healthy controls, the promoter of PDCD1 was hypermethylated (p < 0.001) and the mRNA expression was downregulated (p < 0.001) in AS patients. Significantly negative correlation was identified between the DNA methylation and mRNA expression of PDCD1 gene (r = -0.470, p < 0.001). The receiver operating characteristic (ROC) results showed that PDCD1 island had a sensitivity of 61.3% and a specificity of 82.5%, and PDCD1 mRNA had a sensitivity of 87.2% and a specificity of 89.0%. The methylation level of PDCD1 was positively correlated with the ESR, CRP and ASDAS of AS, and was not affected by HLA-B27 status, gender or medicine intake.
强直性脊柱炎(AS)是一种与自身免疫相关的炎症性关节炎。程序性死亡受体1(PDCD1)基因的DNA甲基化与mRNA表达和AS易感性之间的关联尚不清楚。在这项病例对照研究中,采用甲基化靶向方法检测了80例AS患者和80例健康对照者中PDCD1启动子的甲基化水平。采用实时定量PCR检测了47例AS患者和47例健康对照者中PDCD1基因的转录水平。最终,检测到17个映射到一个CpG岛的甲基化位点。与健康对照相比,AS患者中PDCD1启动子呈高甲基化(p<0.001),mRNA表达下调(p<0.001)。PDCD1基因的DNA甲基化与mRNA表达之间存在显著负相关(r = -0.470,p<0.001)。受试者工作特征(ROC)结果显示,PDCD1岛的敏感性为61.3%,特异性为82.5%,PDCD1 mRNA的敏感性为87.2%,特异性为89.0%。PDCD1的甲基化水平与AS的红细胞沉降率(ESR)、C反应蛋白(CRP)和强直性脊柱炎疾病活动度评分(ASDAS)呈正相关,且不受人类白细胞抗原B27(HLA-B27)状态、性别或药物摄入的影响。