Hassan Wail M, Othman Nashwa, Daghestani Maha, Warsy Arjumand, Omair Maha A, Alqurtas Eman, Amin Shireen, Ismail Abdulaziz, El-Ansary Afaf, Bhat Ramesa Shafi, Omair Mohammed A
Department of Biomedical Sciences, University of Missouri-Kansas City School of Medicine, Kansas City, MO 64108, USA.
Central Research Laboratory, Center for Science and Medical Studies for Girls, King Saud University, Riyadh 11495, Saudi Arabia.
Biomolecules. 2023 Aug 25;13(9):1305. doi: 10.3390/biom13091305.
Rheumatoid arthritis (RA) is an autoimmune inflammatory disease that causes multi-articular synovitis. The illness is characterized by worsening inflammatory synovitis, which causes joint swelling and pain. Synovitis erodes articular cartilage and marginal bone, resulting in joint deterioration. This bone injury is expected to be permanent. Cytokines play a prominent role in the etiology of RA and could be useful as early diagnostic biomarkers. This research was carried out at Riyadh's King Khalid University Hospital (KKUH). Patients were enrolled from the Rheumatology unit. Seventy-eight RA patients were recruited (67 (85.9%) females and 11 (14.1%) males). Patients were selected for participation by convenience sampling. Demographic data were collected, and disease activity measurements at 28 joints were recorded using the disease activity score (DAS-28). Age- and sex-matched controls from the general population were included in the study. A panel of 27 cytokines, chemokines, and growth factors was determined in patient and control sera. Binary logistic regression (BLR) and discriminant analysis (DA) were used to analyze the data. We show that multiple cytokine biomarker profiles successfully distinguished RA patients from healthy controls. IL-17, IL-4, and RANTES were among the most predictive variables and were the only biomarkers incorporated into both BLR and DA predictive models for pooled participants (men and women). In the women-only models, the significant cytokines incorporated in the model were IL-4, IL-17, MIP-1b, and RANTES for the BLR model and IL-4, IL-1Ra, GM-CSF, IL-17, and eotaxin for the DA model. The BLR and DA men-only models contained one cytokine each, eotaxin for BLR and platelet-derived growth factor-bb (PDGF-BB) for DA. We show that BLR has a higher fidelity in identifying RA patients than DA. We also found that the use of gender-specific models marginally improves detection fidelity, indicating a possible benefit in clinical diagnosis. More research is needed to determine whether this conclusion will hold true in various and larger patient populations.
类风湿性关节炎(RA)是一种导致多关节滑膜炎的自身免疫性炎症疾病。该疾病的特征是炎症性滑膜炎不断恶化,进而引起关节肿胀和疼痛。滑膜炎会侵蚀关节软骨和边缘骨,导致关节退化。这种骨质损伤预计是永久性的。细胞因子在类风湿性关节炎的病因中起着重要作用,并且可用作早期诊断生物标志物。本研究在利雅得的哈立德国王大学医院(KKUH)开展。患者来自风湿病科。招募了78例类风湿性关节炎患者(67例(85.9%)女性和11例(14.1%)男性)。通过方便抽样选择患者参与研究。收集了人口统计学数据,并使用疾病活动评分(DAS-28)记录28个关节的疾病活动度测量值。研究纳入了来自普通人群的年龄和性别匹配的对照。测定了患者和对照血清中的一组27种细胞因子、趋化因子和生长因子。使用二元逻辑回归(BLR)和判别分析(DA)来分析数据。我们表明,多种细胞因子生物标志物谱成功地区分了类风湿性关节炎患者和健康对照。白细胞介素-17(IL-17)、白细胞介素-4(IL-4)和调节激活正常T细胞表达和分泌的趋化因子(RANTES)是最具预测性的变量之一,并且是纳入合并参与者(男性和女性)的BLR和DA预测模型的仅有的生物标志物。在仅针对女性的模型中,纳入BLR模型的显著细胞因子为IL-4、IL-17、巨噬细胞炎性蛋白-1β(MIP-1b)和RANTES,纳入DA模型的为IL-4、白细胞介素-1受体拮抗剂(IL-1Ra)、粒细胞巨噬细胞集落刺激因子(GM-CSF)、IL-17和嗜酸性粒细胞趋化因子。仅针对男性的BLR和DA模型各包含一种细胞因子,BLR模型中的为嗜酸性粒细胞趋化因子,DA模型中的为血小板衍生生长因子-BB(PDGF-BB)。我们表明,BLR在识别类风湿性关节炎患者方面比DA具有更高的保真度。我们还发现,使用性别特异性模型在一定程度上提高了检测保真度,这表明在临床诊断中可能有益。需要更多研究来确定这一结论在不同的更大患者群体中是否仍然成立。