Prevalence and Cause of Loss of Visual Acuity and Visual Field in Highly Myopic Eyes The Beijing Eye Study

被引:2
|
作者
Jonas, Jost B. [1 ,2 ,3 ,4 ,5 ]
Jonas, Rahul A. [6 ]
Xu, Jie [1 ]
Wang, Ya Xing [1 ,7 ]
机构
[1] Capital Med Univ, Beijing Inst Ophthalmol, Beijing Tongren Hosp, Beijing Ophthalmol & Visual Sci Key Lab, Beijing, Peoples R China
[2] Heidelberg Univ, Med Fac Mannheim, Dept Ophthalmol, Mannheim, Germany
[3] Privatpraxis Prof Jonas & Dr Panda Jonas, Heidelberg, Germany
[4] Inst Mol & Clin Ophthalmol, Basel, Switzerland
[5] Singapore Eye Res Inst, Singapore, Singapore
[6] Univ Cologne, Dept Ophthalmol, Cologne, Germany
[7] Beijing Tongren Hosp, 1 Dongjiaomin Lane, Beijing 100730, Peoples R China
基金
中国国家自然科学基金;
关键词
Beijing Eye Study; Blindness; High myopia; Myopia; Myopic macular degeneration; Myopic macular neovascularization; Vision loss; OPEN-ANGLE GLAUCOMA; RISK-FACTORS; INTRAOCULAR-PRESSURE; JAPANESE POPULATION; REFRACTIVE ERRORS; ELDERLY CHINESE; GRADING SYSTEM; IMPAIRMENT; CLASSIFICATION; BLINDNESS;
D O I
10.1016/j.ophtha.2023.08.026
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To explore the prevalence and causes of loss of visual acuity and visual field in highly myopic eyes.Design: Population-based study.Participants: 4439 subjects of the Beijing Eye Study underwent ophthalmological and systemic examinations including frequency doubling technology perimetry.Methods: High myopia was defined by a refractive error of <=-6 diopters (D) or axial length >26.0 mm.Main outcome measures: Prevalence of vision impairment causes.Results: 212 highly myopic eyes from 154 participants were included with a mean age of 56.2 +/- 9.6 years, a mean refractive error of -9.87 +/- 3.70 D and a mean axial length of 27.2 +/- 1.3 mm. We observed moderate/severe vision impairment (MSVI) in 40 eyes (18.9%; 95% confidence interval [CI], 13.6-24.2) and blindness in 10 eyes (4.7%; 95% CI, 1.8-7.6). Primary causes for MSVI and blindness were myopic macular degeneration (MMD) (29/50; 58%), age-related macular degeneration (1/50; 2%), and branch macular retinal vein occlusion (1/50; 2%). Secondary causes were MMD (4/50; 8%) and optic nerve atrophy (14/50, 28%), further differentiated into non-glaucomatous optic atrophy (NGOA) (9/50; 18%) and glaucomatous optic atrophy (GOA) (5/50; 10%). Prevalence of MMD as vision impairment cause increased significantly from 1/61 (1.6%) in the refractive error group of -6.00 to >=-7.00 D, to 16/25 (64%) in the group of <-15.0 D. Higher MMD prevalence correlated with higher myopic refractive error (P < 0.001) and increased likelihood of concomitant optic neuropathy (P < 0.001). Similarly, prevalence of optic neuropathy as vision impairment cause increased from 0/61 (0%) in the refractive error group of -6.00 D to >=-7.00 D, to 9/25 (36%) in the group of <-15.0 D. Higher optic neuropathy prevalence correlated with more myopic refraction (P < 0.001) and older age (P = 0.02).Conclusions: In this population-based recruited cohort of highly myopic patients, optic neuropathy accounted for vision impairment in 9.0% eyes, which was lower than the prevalence of MMD as vision impairment cause (18.9%). Notably, optic neuropathy became a significant contributor to vision impairment in more advanced high myopia, reaching 36% in the group with refractive error of <-15.0 D.Financial disclosure(s): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.(c) 2023 by the American Academy of Ophthalmology
引用
收藏
页码:58 / 65
页数:8
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