Department of Biochemistry, Faculty of Pharmacy, Cairo University, 11562, Cairo, Egypt.
Department of Rheumatology and Clinical Immunology, Internal Medicine, Kasr Al- Ainy, Faculty of Medicine, Cairo University, Cairo, Egypt.
BMC Med Genomics. 2023 Aug 29;16(1):204. doi: 10.1186/s12920-023-01635-3.
The genetic architecture of rheumatoid arthritis (RA) and osteoarthritis (OA) are still unclear. Although RA and OA have quite different causes, they share synovial inflammation, risk factors, and some disease-associated genes, including the integrin subunit β2 (ITGB2)/CD18 gene involved in extracellular matrix interactions and immune cell signaling. However, the functional role of ITGB2 genetic variants, its circulating expression pattern, and their clinical usefulness in RA and OA remain unexplored. Our study appraised the association of ITGB2 rs2070946 single nucleotide polymorphism with the vulnerability to RA and OA and its influence on ITGB2 mRNA expression, along with the potential of serum ITGB2 expression in RA and OA diagnosis.
This study included 70 RA patients, 70 primary OA patients, and 60 healthy volunteers. Genotyping and gene expression analysis were performed using qPCR. Bioinformatics analysis was employed to construct the protein-protein interaction (PPI) network of ITGB2.
Serum ITGB2 mRNA expression was upregulated in both RA and OA compared to healthy controls. ITGB2 rs2070946 was associated with escalating risk of both diseases. RA patients harboring the rs2070946 CC or TC + CC genotypes had higher serum ITGB2 expression than the TT genotype carriers. Likewise, OA patients having the minor homozygote CC genotype had higher serum ITGB2 expression than those carrying the TT, TC or TT + TC genotypes. Serum ITGB2 expression showed profound diagnostic potential for RA and OA in receiver-operating characteristic analysis. In RA, serum ITGB2 expression positively correlated with rheumatoid factor and disease activity score 28 (DAS28). The ITGB2-PPI network enriched in cell-cell adhesion, ICAM-3 receptor activity, T-cell activation, leukocyte adhesion, complement binding, and NF-κB, tumor necrosis factor, and interleukin signaling pathways.
These findings embrace the impact of ITGB2 rs2070946 as a novel genetic biomarker of both RA and OA, which could alter the ITGB2 expression. Serum ITGB2 expression could aid in timely diagnosis of RA and OA.
类风湿关节炎(RA)和骨关节炎(OA)的遗传结构仍不清楚。虽然 RA 和 OA 的病因截然不同,但它们都具有滑膜炎症、危险因素和一些与疾病相关的基因,包括参与细胞外基质相互作用和免疫细胞信号的整合素亚基β2(ITGB2)/CD18 基因。然而,ITGB2 遗传变异的功能作用、其循环表达模式及其在 RA 和 OA 中的临床应用价值仍未得到探索。我们的研究评估了 ITGB2 rs2070946 单核苷酸多态性与 RA 和 OA 易感性的关系及其对 ITGB2 mRNA 表达的影响,以及血清 ITGB2 表达在 RA 和 OA 诊断中的潜力。
本研究纳入了 70 例 RA 患者、70 例原发性 OA 患者和 60 名健康志愿者。使用 qPCR 进行基因分型和基因表达分析。采用生物信息学分析构建 ITGB2 蛋白-蛋白相互作用(PPI)网络。
与健康对照组相比,RA 和 OA 患者的血清 ITGB2 mRNA 表达均上调。ITGB2 rs2070946 与两种疾病的风险增加有关。携带 rs2070946 CC 或 TC+CC 基因型的 RA 患者血清 ITGB2 表达高于 TT 基因型携带者。同样,携带 CC 纯合子的 OA 患者血清 ITGB2 表达高于携带 TT、TC 或 TT+TC 基因型的患者。在 RA 中,血清 ITGB2 表达在受试者工作特征分析中具有显著的诊断潜力。在 RA 中,血清 ITGB2 表达与类风湿因子和 28 天疾病活动评分(DAS28)呈正相关。ITGB2-PPI 网络富集于细胞-细胞黏附、ICAM-3 受体活性、T 细胞激活、白细胞黏附、补体结合以及 NF-κB、肿瘤坏死因子和白细胞介素信号通路。
这些发现表明 ITGB2 rs2070946 是 RA 和 OA 的新型遗传生物标志物,可能改变 ITGB2 的表达。血清 ITGB2 表达有助于 RA 和 OA 的及时诊断。