Association of GNB3, ACE polymorphisms with POAG and NTG.

IF 1.2 4区 医学 Q4 GENETICS & HEREDITY
Ophthalmic Genetics Pub Date : 2024-02-01 Epub Date: 2024-01-26 DOI:10.1080/13816810.2023.2283415
Alexander N Samoylov, Polina Tumanova, Sofya A Pankratova, Liana Sh Ashryatova, Denis Plotnikov
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引用次数: 0

Abstract

Purpose: Primary open-angle glaucoma (POAG) represents the most prevalent form of glaucoma and stands as a foremost contributor to irreversible vision impairment on a global scale. Despite notable strides made in comprehending the genetic underpinnings of POAG, investigations within the context of Russia remain constrained.

Methods: The study cohort comprised a total of 235 individuals, with 135 of them exhibiting various forms of glaucoma encompassing both POAG and (NTG, while the remaining 100 individuals served as control subjects. Each participant underwent a comprehensive ocular examination to ascertain their ocular health status. Genotyping of the relevant single nucleotide polymorphisms (SNPs) was carried out using the Taq Man genotyping assay. Specifically, the two SNPs under scrutiny were GNB3 rs5443 gene and ACE rs4646994. Statistical analysis was performed to evaluate the association of these SNPs with glaucoma risk.

Results: The presence of the T allele of rs5443 was found to be associated with NTG (p = .004). However, no statistically significant correlation was identified between this SNP and POAG (p = .88).

Conclusion: This study provides evidence of an association between the T allele of rs5443 and a reduced susceptibility NTG within the Russian population. These observations augment the comprehension of the genetic underpinnings of glaucoma and hold potential implications for the prospective development of targeted therapeutic interventions.

GNB3、ACE多态性与POAG和NTG的关联
目的:原发性开角型青光眼(POAG)是最常见的青光眼,是全球范围内造成不可逆视力损害的主要原因。尽管在理解POAG的遗传基础方面取得了显着进步,但在俄罗斯背景下的调查仍然受到限制。方法:研究队列共包括235人,其中135人表现出包括POAG和(NTG)在内的各种形式的青光眼,而其余100人作为对照组。每位参与者都进行了全面的眼部检查,以确定他们的眼部健康状况。使用Taq Man基因分型法对相关单核苷酸多态性(snp)进行基因分型。具体来说,这两个snp是GNB3 rs5443基因和ACE rs4646994。统计分析这些snp与青光眼风险的关系。结果:rs5443 T等位基因的存在与NTG相关(p = 0.004)。然而,该SNP与POAG之间没有统计学上的显著相关性(p = 0.88)。结论:本研究为俄罗斯人群中rs5443等位基因T与NTG易感性降低之间的关联提供了证据。这些观察结果增强了对青光眼遗传基础的理解,并对靶向治疗干预的前瞻性发展具有潜在的意义。
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
Ophthalmic Genetics
Ophthalmic Genetics 医学-眼科学
CiteScore
2.40
自引率
8.30%
发文量
126
审稿时长
>12 weeks
期刊介绍: Ophthalmic Genetics accepts original papers, review articles and short communications on the clinical and molecular genetic aspects of ocular diseases.
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