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中国小眼球继发闭角型青光眼队列中的基因谱及基因型-表型相关性

Genetic Spectrum and Genotype-Phenotype Correlations in a Chinese Cohort With Nanophthalmos With Secondary Angle-Closure Glaucoma.

作者信息

Yu Xiaowei, Zhao Hanxue, Gao Yan, Zhou Tao, Deng Lin, Zhang Miao, Zhong Hongyu, Mei Feng, Li Zhijun, Sun Longyan, Zhang Tianrui, Shi Yan, Fan Zhigang

机构信息

Beijing Tongren Eye Center Research Ward, Beijing Tongren Hospital, Beijing Institute of Ophthalmology, Beijing Ophthalmology & Visual Sciences Key Laboratory, Capital Medical University, Beijing, China.

出版信息

Invest Ophthalmol Vis Sci. 2025 Jun 2;66(6):9. doi: 10.1167/iovs.66.6.9.

Abstract

PURPOSE

The purpose of this study was to explore the genetic and clinical features of nanophthalmos with secondary angle-closure glaucoma (NSACG) in a Chinese cohort. This was a prospective cross-sectional study of 157 eyes from 88 Chinese patients with NSACG.

METHODS

The participants underwent ocular and systemic examinations and whole-exome sequencing. The main outcome measures were pathogenic genetic variants, axial length (AL), refractive spherical equivalent (SE), vitreous chamber depth (VCD), white-to-white (WTW), radius of corneal curvature (flat and steep K: K1 and K2), anterior chamber depth (ACD), lens vault (LV), lens thickness (LT), extent of angle closure, anterior segment crowding value, retinal nerve fiber layer (RNFL) thickness, central subfield thickness (CST) in macular, cup-to-disc ratio (C/D), mean defect in visual field, and onset age of angle-closure glaucoma (ACG).

RESULTS

Seventy-eight variants (51.14%) were identified in 45 patients, including 20 in PRSS56 (44.44%) and 14 in MFRP (31.11%) with autosomal recessive (AR) inheritance, 8 in MYRF (17.78%), and 3 in TMEM98 (6.6%) with autosomal dominant (AD) inheritance. Individuals with genetic diagnosis were associated with shorter AL, higher SE, larger K1 and K2, shallower ACD, greater angle closure extent, larger LT/AL, shorter VCD, and higher incidence of retinal detachment. Compared with AR cases, patients with AD showed younger ACG onset, longer AL, lower SE, smaller K1 and K2, longer VCD, thinner CST of the macula, and more severe visual field defects.

CONCLUSIONS

Among Chinese patients with NSACG, PRSS56 and MFRP were the predominant AR variants, whereas MYRF and TMEM98 were the main AD variants. Genetic diagnosis exhibited shorter AL and a more crowded anterior segment, leading to accelerated glaucoma progression. The faster glaucoma progression in AD cases highlights the need for early intervention.

摘要

目的

本研究旨在探讨中国人群中合并继发性闭角型青光眼的小眼球(NSACG)的遗传和临床特征。这是一项对88例中国NSACG患者的157只眼睛进行的前瞻性横断面研究。

方法

参与者接受了眼部和全身检查以及全外显子测序。主要观察指标为致病基因变异、眼轴长度(AL)、等效球镜度(SE)、玻璃体腔深度(VCD)、角膜水平直径(WTW)、角膜曲率半径(平坦和陡峭K值:K1和K2)、前房深度(ACD)、晶状体高度(LV)、晶状体厚度(LT)、房角关闭程度、眼前节拥挤值、视网膜神经纤维层(RNFL)厚度、黄斑中心子野厚度(CST)、杯盘比(C/D)、视野平均缺损以及闭角型青光眼(ACG)的发病年龄。

结果

在45例患者中鉴定出78个变异(51.14%),其中常染色体隐性(AR)遗传的PRSS56基因中有20个变异(44.44%),MFRP基因中有14个变异(31.11%),常染色体显性(AD)遗传的MYRF基因中有8个变异(17.78%),TMEM98基因中有3个变异(6.6%)。基因诊断个体与较短的AL、较高的SE、较大的K1和K2、较浅的ACD、更大的房角关闭程度、更大的LT/AL、较短的VCD以及更高视网膜脱离发生率相关。与AR病例相比,AD患者的ACG发病年龄更小、AL更长、SE更低、K1和K2更小、VCD更长、黄斑CST更薄以及视野缺损更严重。

结论

在中国NSACG患者中,PRSS56和MFRP是主要的AR变异基因,而MYRF和TMEM98是主要的AD变异基因。基因诊断显示AL较短且眼前节更拥挤,导致青光眼进展加速。AD病例中青光眼进展更快凸显了早期干预的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d393/12136104/5e5bd633173c/iovs-66-6-9-f001.jpg

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