Nateghi Ali, Zamani Samin, Tahamtan Alireza
Department of Microbiology, Golestan University of Medical Sciences, Gorgan, Iran.
Golestan Rheumatology Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Int J Genomics. 2025 Jun 16;2025:6182868. doi: 10.1155/ijog/6182868. eCollection 2025.
Rheumatoid arthritis (RA) is a chronic autoimmune disease primarily affecting the joints. The endocannabinoid system plays a crucial role in maintaining immune balance by regulating immune functions. Variations in the CB2 receptor gene () can disrupt intracellular signaling, impairing the regulatory functions of endocannabinoids. This dysfunction is associated with an imbalanced immune response and an increased risk of autoimmune inflammatory disorders. This study investigates, for the first time in an Iranian population, the association between the Q63R polymorphism in the gene and RA. A total of 120 RA patients and 120 healthy controls were genotyped using the TaqMan assay. Demographic and clinical data, including gender, age, and ethnicity, were collected through questionnaires. The codominant, dominant, recessive, overdominant, and additive inheritance models were analyzed using SNPStats software. Logistic regression analysis revealed significant associations under the codominant, dominant, and additive inheritance models, with RR genotype carriers exhibiting more than a 2.5-fold increased risk of developing RA. The findings of this study suggest a potential role of the gene in RA susceptibility among Iranian patients. However, further large-scale studies are required to better understand the contribution of the CB2 receptor to disease susceptibility and its potential clinical applications as a biomarker for diagnosis and therapeutic interventions.
类风湿性关节炎(RA)是一种主要影响关节的慢性自身免疫性疾病。内源性大麻素系统通过调节免疫功能在维持免疫平衡中发挥关键作用。CB2受体基因()的变异会破坏细胞内信号传导,损害内源性大麻素的调节功能。这种功能障碍与免疫反应失衡和自身免疫性炎症疾病风险增加有关。本研究首次在伊朗人群中调查了基因中Q63R多态性与RA之间的关联。使用TaqMan分析法对120例RA患者和120例健康对照进行基因分型。通过问卷调查收集人口统计学和临床数据,包括性别、年龄和种族。使用SNPStats软件分析共显性、显性、隐性、超显性和加性遗传模型。逻辑回归分析显示,在共显性、显性和加性遗传模型下存在显著关联,RR基因型携带者患RA的风险增加超过2.5倍。本研究结果表明该基因在伊朗患者RA易感性中可能起作用。然而,需要进一步的大规模研究,以更好地了解CB2受体对疾病易感性的贡献及其作为诊断和治疗干预生物标志物的潜在临床应用。