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与原发性开角型青光眼视野丧失相关的遗传变异。

Genetic variants associated with glaucomatous visual field loss in primary open-angle glaucoma.

机构信息

Department of Ophthalmology, Faculty of Medicine, University of Yamanashi, Chuo, Yamanashi, Japan.

Department of Health Sciences, Faculty of Medicine, University of Yamanashi, Chuo, Yamanashi, Japan.

出版信息

Sci Rep. 2022 Dec 1;12(1):20744. doi: 10.1038/s41598-022-24915-x.

Abstract

Primary open-angle glaucoma (POAG) is characterized by a progressive optic neuropathy with visual field loss. To investigate the genetic variants associated with visual field loss in POAG, Japanese POAG patients (n = 426) and control subjects (n = 246) were genotyped for 22 genetic variants predisposing to POAG that can be classified into those associated with intraocular pressure (IOP) elevation (IOP-related genetic variants) and optic nerve vulnerability independent of IOP (optic nerve-related genetic variants). The genetic risk score (GRS) of the 17 IOP-related and five optic nerve-related genetic variants was calculated, and the associations between the GRS and the mean deviation (MD) of automated static perimetry as an indicator of the severity of visual field loss and pattern standard deviation (PSD) as an indicator of the focal disturbance were evaluated. There was a significant association (Beta = - 0.51, P = 0.0012) between the IOP-related GRS and MD. The severity of visual field loss may depend on the magnitude of IOP elevation induced by additive effects of IOP-related genetic variants. A significant association (n = 135, Beta = 0.65, P = 0.0097) was found between the optic nerve-related, but not IOP-related, GRS and PSD. The optic nerve-related (optic nerve vulnerability) and IOP-related (IOP elevation) genetic variants may play an important role in the focal and diffuse visual field loss respectively. To our knowledge, this is the first report to show an association between additive effects of genetic variants predisposing to POAG and glaucomatous visual field loss, including severity and focal/diffuse disturbance of visual field loss, in POAG.

摘要

原发性开角型青光眼(POAG)的特征是视神经进行性病变伴视野丧失。为了研究与 POAG 视野丧失相关的遗传变异,对 426 例日本 POAG 患者和 246 例对照进行了 22 个易患 POAG 的遗传变异的基因分型,这些变异可分为与眼压升高(IOP 相关遗传变异)和独立于 IOP 的视神经易损性(视神经相关遗传变异)相关的遗传变异。计算了 17 个 IOP 相关和 5 个视神经相关遗传变异的遗传风险评分(GRS),并评估了 GRS 与自动静态视野计的平均偏差(MD)(作为视野丧失严重程度的指标)和模式标准差(PSD)(作为视野局部干扰的指标)之间的关系。IOP 相关 GRS 与 MD 之间存在显著相关性(Beta=-0.51,P=0.0012)。视野丧失的严重程度可能取决于 IOP 相关遗传变异的累加效应对眼压升高的影响程度。视神经相关 GRS 与 PSD 之间存在显著相关性(n=135,Beta=0.65,P=0.0097),而 IOP 相关 GRS 与 PSD 无显著相关性。视神经相关(视神经易损性)和 IOP 相关(IOP 升高)遗传变异可能分别在局灶性和弥漫性视野丧失中发挥重要作用。据我们所知,这是第一项报告显示 POAG 易患遗传变异的累加效应对 POAG 中青光眼视野丧失(包括视野丧失的严重程度和局灶/弥漫性干扰)的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2edd/9715669/c1bcf6714d27/41598_2022_24915_Fig1_HTML.jpg

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