活动性类风湿关节炎中TNF-α与IL-6基因表达水平:临床和实验室决定因素

Enas I Abdelhady, Hanaa I Abd El-Hady, Shahenda G Badran, Mona Rabie
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摘要

本研究旨在比较肿瘤坏死因子-α (TNF-α)和白细胞介素6 (IL-6)基因在接受常规合成疾病改善药物(csDMARDs)治疗的活动性类风湿关节炎(RA)患者中的表达水平,并寻找影响活动性类风湿关节炎患者中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,包括108名接受csDMARDs治疗的活动性RA患者。除了完整的体格检查和28关节疾病活动评分(DAS28)评估外,还对所有患者进行了详细的病史回顾。记录c反应蛋白(CRP)、红细胞沉降率(ESR)、血清类风湿因子(RF)等实验室指标。采用实时定量聚合酶链反应(qRT-PCR)检测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基因表达水平具有显著相关性(p<0.001, r=0.788)。此外,两者与RA患者的年龄和DAS28呈正相关(p<0.001)。DAS28评分高的RA患者IL-6和TNF-α表达水平显著升高(p<0.001)。大多数RA患者(81.5%)IL-6基因表达水平高于TNF-α。与TNF-α基因表达水平较高的RA患者相比,IL-6基因表达水平较高的RA患者年龄较轻,病程较短,DAS28较低。此外,他们有更高的CRP和RF水平。与TNF-α相比,年轻年龄是IL-6基因表达水平相对较高的显著预测因子。结论:大多数活动期RA患者IL-6基因表达水平高于TNF-α。年轻可以被认为是活动期RA患者中相对较高的IL-6基因表达水平的重要预测因子。
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TNF-α versus IL-6 Genes Expression levels in Active Rheumatoid Arthritis: Clinical and Laboratory Determinants
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.
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