Department of Rheumatology and Rehabilitation, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Department Medical Microbiology and Immunology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Egypt J Immunol. 2023 Oct;30(4):1-10.
This study intended to compare the expression levels of tumor necrosis factor-alpha (TNF-α) and interleukin 6 (IL-6) genes in active rheumatoid arthritis (RA) patients who were receiving conventional synthetic disease-modifying drugs (csDMARDs) and to find the clinical and laboratory determinants affecting TNF-α and IL-6 genes expression levels among active RA patients. This was a cross sectional study that included 108 active RA patients who were receiving csDMARDs. A detailed history was reviewed for all patients in addition to a complete physical examination and assessment of the 28-joint disease activity score (DAS28). Some laboratory measures were recorded as C-reactive protein (CRP), erythrocyte sedimentation rate (ESR) and serum rheumatoid factor (RF). Quantitative real-time polymerase chain reaction (qRT-PCR) was used to measure expression levels of TNF- α and IL-6 genes. In active RA patients, TNF-α and IL-6 genes expression levels were significantly correlated to each other (p<0.001, r=0.788). Also, both had positive correlations with the age and DAS28 among RA patients (p<0.001). IL-6 and TNF-α expression levels were significantly higher in RA patients with high DAS28 scores (p<0.001). Most RA patients (81.5%) had relatively higher IL-6 gene expression levels than TNF-α. RA patients with relatively high IL-6 expression levels were younger in age and had shorter disease duration and less DAS28 than RA patients with relatively high TNF-α gene expression levels. In addition, they had higher CRP and RF levels. Young age was detected as a significant predictor for relatively higher IL-6 gene expression levels than TNF-α. In conclusion, most active RA patients had higher IL-6 gene expression levels than TNF-α. Young age could be considered a significant predictor for relatively high IL-6 gene expression levels among active RA patients.
本研究旨在比较接受传统合成疾病修饰药物(csDMARDs)治疗的活动期类风湿关节炎(RA)患者肿瘤坏死因子-α(TNF-α)和白细胞介素 6(IL-6)基因的表达水平,并找出影响活动期 RA 患者 TNF-α和 IL-6 基因表达水平的临床和实验室决定因素。这是一项横断面研究,共纳入 108 例接受 csDMARDs 治疗的活动期 RA 患者。对所有患者进行详细的病史回顾,同时进行全面的体格检查和 28 关节疾病活动评分(DAS28)评估。记录一些实验室指标,包括 C 反应蛋白(CRP)、红细胞沉降率(ESR)和血清类风湿因子(RF)。采用实时定量聚合酶链反应(qRT-PCR)测量 TNF-α和 IL-6 基因的表达水平。在活动期 RA 患者中,TNF-α和 IL-6 基因的表达水平呈显著正相关(p<0.001,r=0.788)。此外,这两个基因与 RA 患者的年龄和 DAS28 均呈正相关(p<0.001)。DAS28 评分较高的 RA 患者的 IL-6 和 TNF-α表达水平显著升高(p<0.001)。大多数 RA 患者(81.5%)的 IL-6 基因表达水平相对较高,而 TNF-α基因表达水平相对较低。与 TNF-α基因表达水平较高的 RA 患者相比,IL-6 表达水平较高的 RA 患者年龄较小,病程较短,DAS28 较低。此外,他们的 CRP 和 RF 水平较高。年龄较轻被检测为 IL-6 基因表达水平相对较高而非 TNF-α的显著预测因素。总之,大多数活动期 RA 患者的 IL-6 基因表达水平高于 TNF-α。年龄较轻可被视为活动期 RA 患者中 IL-6 基因表达水平较高的重要预测因素。