Beijing Institute of Ophthalmology, Beijing Tongren Hospital, Capital Medical University, Beijing Ophthalmology and Visual Sciences Key Laboratory, Beijing, China; Department of Ophthalmology, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany; Privatpraxis Prof Jonas und Dr Panda-Jonas, Heidelberg, Germany; Institute of Molecular and Clinical Ophthalmology, Basel, Switzerland; Singapore Eye Research Institute, Singapore.
Department of Ophthalmology, University of Cologne, Cologne, Germany.
Ophthalmology. 2024 Jan;131(1):58-65. doi: 10.1016/j.ophtha.2023.08.026. Epub 2023 Sep 9.
To explore the prevalence and causes of loss of visual acuity and visual field in highly myopic eyes.
Population-based study.
4439 subjects of the Beijing Eye Study underwent ophthalmological and systemic examinations including frequency doubling technology perimetry.
High myopia was defined by a refractive error of ≤-6 diopters (D) or axial length >26.0 mm.
Prevalence of vision impairment causes.
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).
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.
探讨高度近视眼中视力丧失和视野丧失的患病率和原因。
基于人群的研究。
北京眼病研究中 4439 名受试者接受了眼科和全身检查,包括频域光相干断层扫描。
近视定义为屈光不正≤-6 屈光度(D)或眼轴长度>26.0mm。
视力损害原因的患病率。
纳入了 154 名参与者的 212 只高度近视眼,平均年龄为 56.2±9.6 岁,平均屈光度为-9.87±3.70D,平均眼轴长度为 27.2±1.3mm。我们观察到 40 只眼(18.9%;95%置信区间[CI],13.6-24.2)有中度/重度视力损害(MSVI)和 10 只眼(4.7%;95%CI,1.8-7.6)失明。MSVI 和失明的主要原因是近视性黄斑变性(MMD)(29/50;58%)、年龄相关性黄斑变性(1/50;2%)和分支黄斑视网膜静脉阻塞(1/50;2%)。次要原因是 MMD(4/50;8%)和视神经萎缩(14/50,28%),进一步分为非青光眼性视神经萎缩(NGOA)(9/50;18%)和青光眼性视神经萎缩(GOA)(5/50;10%)。MMD 作为视力损害原因的患病率随着近视屈光度的增加而显著增加,从-6.00 至≥-7.00D 的屈光误差组的 1/61(1.6%)增加到<-15.0D 的组的 16/25(64%)。较高的 MMD 患病率与较高的近视屈光不正(P<0.001)和并发视神经病变的可能性增加相关(P<0.001)。同样,视神经病变作为视力损害原因的患病率从-6.00D 的屈光误差组的 0/61(0%)增加到<-15.0D 的组的 9/25(36%)。较高的视神经病变患病率与更高度近视的屈光度增加(P<0.001)和年龄较大(P=0.02)相关。
在这项基于人群招募的高度近视患者队列研究中,视神经病变导致 9.0%的眼睛视力受损,低于 MMD 作为视力损害原因的患病率(18.9%)。值得注意的是,视神经病变在更严重的高度近视中成为视力损害的一个重要因素,在屈光误差<-15.0D 的组中达到 36%。