Association of TNF-α gene promoter polymorphism with primary open-angle glaucoma

Q4 Medicine
A. Shevchenko, V. F. Prokof’ev, V. I. Konenkov, A. Eremina, A. Trunov, V. Chernykh
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引用次数: 0

Abstract

Background: glaucoma is one of the leading causes of blindness worldwide. Diagnosis of glaucoma at an early stage is challenging. Therefore, genetic factors predisposing to the development of primary open-angle glaucoma (POAG) are investigated. One of these predictors is tumor necrosis factor α (TNFα), a multifunctional proinflammatory cytokine involved in glaucoma pathogenesis. Point mutations in the regulatory region of the TNFα gene are hypothesized to be associated with POAG risk. Aim: to analyze the polymorphism of three positions of TNFα gene promoters and their complexes in West Siberian Caucasians with POAG and healthy volunteers. Patients and Methods: the study enrolled 401 individuals, i.e., 99 patients with POAG stage 2 and 302 individuals without POAG (randomized control group). All participants signed an informed consent form. Single nucleotide TNFα gene promoter polymorphism (rs361525, rs1800629, rs1800630) was analyzed. Genotyping was performed by restriction analysis of gene amplification products. Results: the occurrence of minor genotype TNF-308*АА was significantly higher in POAG (odds ratio 11.41, p=0.0011). The occurrence of two other genotypes demonstrated no significant differences between groups. Three complex genotypes were positively associated with POAG (TNF-863*CC:TNF-308*AA, TNF-308*AA:TNF-238*GG и TNF-863*CC:TNF-308*AA:TNF-238*GG). We failed to identify any single nucleotide polymorphism or complexes negatively associated with POAG. Conclusion: minor genotype TNF-308*АА is an essential factor of POAG pathogenesis. Two other polymorphic gene variants were associated with POAG as a part of complex genotypes. These findings demonstrate that potential polymorphic associations should be considered in the case-control analysis. Keywords: primary open-angle glaucoma, polymorphism, TNFα gene, gene promoter, complex genotypes. For citation: Shevchenko A.V., Prokof’ev V.F., Konenkov V.I. et al. Association of TNF-α gene promoter polymorphism with primary open-angle glaucoma. Russian Journal of Clinical Ophthalmology. 2022;22(1):11–15 (in Russ.). DOI: 10.32364/2311-7729-2022-22-1-11-15.
TNF-α基因启动子多态性与原发性开角型青光眼的关系
背景:青光眼是全球致盲的主要原因之一。青光眼的早期诊断是具有挑战性的。因此,对原发性开角型青光眼(POAG)的遗传易感性进行了研究。其中一个预测因子是肿瘤坏死因子α (TNFα),这是一种参与青光眼发病的多功能促炎细胞因子。TNFα基因调控区域的点突变被认为与POAG风险相关。目的:分析西西伯利亚白种人POAG患者与健康志愿者中TNFα基因启动子及其复合物3个位点的多态性。患者和方法:本研究共纳入401例患者,即2期POAG患者99例,非POAG患者302例(随机对照组)。所有参与者都签署了知情同意书。单核苷酸tnf - α基因启动子多态性(rs361525, rs1800629, rs1800630)分析。基因扩增产物限制性内切分析进行基因分型。结果:小基因型TNF-308*АА在POAG中的发生率显著增高(优势比11.41,p=0.0011)。另外两种基因型的发生在组间无显著差异。3种复合基因型与POAG呈正相关(TNF-863*CC:TNF-308*AA, TNF-308*AA:TNF-238*GG, TNF-863*CC:TNF-308*AA:TNF-238*GG)。我们没有发现任何与POAG负相关的单核苷酸多态性或复合物。结论:小基因型TNF-308*АА是POAG发病的重要因素。另外两种多态基因变异作为复杂基因型的一部分与POAG相关。这些发现表明,在病例对照分析中应考虑潜在的多态性关联。关键词:原发性开角型青光眼,多态性,TNFα基因,基因启动子,复杂基因型引文:舍甫琴科a.v.,普罗科夫v.f.,科南科夫V.I.等。TNF-α基因启动子多态性与原发性开角型青光眼的关系。俄罗斯临床眼科杂志,2022;22(1):11-15(俄文)。DOI: 10.32364 / 2311-7729-2022-22-1-11-15。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
21
审稿时长
20 weeks
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