Department of Nephrology, Faculty of Medicine, School of Health Sciences, University of Thessaly, 41500 Larissa, Greece.
First Department of Ophthalmology, Faculty of Health Sciences, Aristotle University of Thessaloniki School of Medicine, AHEPA Hospital, 54636 Thessaloniki, Greece.
Genes (Basel). 2023 Jul 21;14(7):1488. doi: 10.3390/genes14071488.
Tumor necrosis factor-α (TNF-α) is a potent pro-inflammatory cytokine, involved in the pathogenesis and progression of immunoglobulin A nephropathy (IgAN). A bi-allelic polymorphism in the promoter region, at position -308 (G/A) of the - gene (rs1800629) is associated with an increased TNF-a production. However, several previous association studies of - G-308A polymorphism and IgAN rendered contradictory findings. The objective of the present study is to shed light on these inconclusive results and clarify the role of TNF-α and any possible contribution of this factor in the development and progression of sporadic IgAN. Therefore, a meta-analysis of all available genetic association studies relating the G-308A polymorphism to the risk for development and/or progression of IgAN was conducted. Seven studies were included in the meta-analysis. Three of them included populations of European descent (Caucasians) and four involved Asians. The generalized odds ratio (OR) was used to estimate the risk for the development and/or progression of the disease. Overall, the meta-analysis did not detect any significant association between the G-308A variant and both the risk of developing IgAN and the risk for progression of IgAN. In conclusion, these results suggest that does not constitute a key component in the genetic architecture of sporadic IgAN. However, further evidence deciphering the influence of on IgAN is still needed.
肿瘤坏死因子-α(TNF-α)是一种有效的促炎细胞因子,参与免疫球蛋白 A 肾病(IgAN)的发病机制和进展。- 基因启动子区域位置-308(G/A)的双等位基因多态性(rs1800629)与 TNF-α产生增加有关。然而,先前几项关于- G-308A 多态性与 IgAN 的关联研究得出了相互矛盾的结果。本研究旨在阐明这些不确定的结果,并阐明 TNF-α的作用以及该因素在散发性 IgAN 的发生和进展中的任何可能作用。因此,对所有与 G-308A 多态性与 IgAN 的发展和/或进展风险相关的遗传关联研究进行了荟萃分析。该荟萃分析共纳入了 7 项研究。其中 3 项研究纳入了欧洲裔人群(白种人),4 项研究涉及亚洲人。广义优势比(OR)用于估计疾病发展和/或进展的风险。总体而言,荟萃分析未发现 G-308A 变体与 IgAN 的发展风险和 IgAN 的进展风险之间存在任何显著关联。总之,这些结果表明,TNF-α 并非散发性 IgAN 遗传结构的关键组成部分。然而,仍需要进一步的证据来阐明 TNF-α对 IgAN 的影响。