老年高度近视患者角膜内皮细胞的特征。

IF 3.7 Q2 GENETICS & HEREDITY
Phenomics (Cham, Switzerland) Pub Date : 2025-01-27 eCollection Date: 2024-12-01 DOI:10.1007/s43657-024-00186-6
Yinglei Zhang, Shaohua Zhang, Keke Zhang, Yi Lu, Xiangjia Zhu
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引用次数: 0

摘要

本横断面研究旨在探讨老年高度近视患者角膜内皮的特征。我们使用非接触式镜面显微镜对1065例老年患者(549只高度近视眼和516只对照眼)的1065只眼的角膜内皮特征进行了评估。用裂隙灯和共聚焦显微镜确认疑似Fuchs内皮性角膜营养不良(FECD)。高度近视眼的中心内皮细胞密度(ECD)和变异系数(CV)显著增加(p = 0.001和p = 0.002),平均细胞面积(AVG)和六边形百分比(HEX)显著降低(p = 0.014和p = 0.130, p = 0.113, p = - 0.105, p = 0.001和r = - 0.204, p = 0.036)。综上所述,较长的AL与老年患者角膜ECD增加以及内皮多形性和多聚性增加有关。高度近视眼有较高的FECD患病率和严重程度。该研究于2017年2月26日在www.clinicaltrials.gov上注册,注册号为NCT03062085。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics of the Corneal Endothelium in Elderly Adults with High Myopia.

This cross-sectional study aimed to investigate the corneal endothelial characteristics in elderly individuals with high myopia. We assessed corneal endothelial characteristics in 1065 eyes of 1065 elderly patients (549 highly myopic and 516 control eyes) using non-contact specular microscopy. Confirmation of suspected Fuchs endothelial corneal dystrophy (FECD) was performed with slit-lamp and confocal microscopy. Highly myopic eyes exhibited significantly greater central endothelial cell density (ECD) and coefficient of variation (CV) (p = 0.001 and p = 0.002, respectively), and lower average cell area (AVG) and percent of hexagonality (HEX) (p = 0.014 and p < 0.001, respectively) compared to control eyes. After adjusting for age and gender, axial length (AL) was positively correlated with ECD and CV (r = 0.130, p < 0.001 and r = 0.113, p < 0.001, respectively), and was negatively correlated with AVG and HEX (r = - 0.105, p = 0.001 and r = - 0.204, p < 0.001, respectively). FECD prevalence was 4.92% in highly myopic eyes and 3.29% in controls, with more advanced cases in highly myopic eyes (p = 0.036). In conclusion, longer AL was associated with increased corneal ECD, and greater endothelial pleomorphism and polymegethism in elderly patients. Highly myopic eyes appeared to have higher prevalence and severity of FECD. The study was registered on www.clinicaltrials.gov on February 26, 2017, with the registration number NCT03062085.

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