Longitudinal Progression of Myopic Maculopathy in a Long-Term Follow-Up of a European Cohort

IF 5.9 Q1 OPHTHALMOLOGY Ophthalmology. Retina Pub Date : 2025-08-01 Epub Date: 2025-02-24 DOI:10.1016/j.oret.2025.02.015
Matteo Mario Carlà MD , Francesco Boselli MD , Federico Giannuzzi MD , Emanuele Crincoli MD , Fiammetta Catania MD , Tomaso Caporossi MD, PhD , Stanislao Rizzo MD , Carlos Mateo MD
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Abstract

Purpose

To evaluate the longitudinal progression of myopic maculopathy in a European cohort of highly myopic patients, analyzing the disease natural history and its impact on visual function.

Design

Retrospective, observational monocentric cohort study.

Participants

The study included 1228 eyes from 781 highly myopic patients with a minimum follow-up time of 5 years. We collected best-corrected visual acuity (BCVA) measurement, axial length (AXL), fundus photography, and spectral-domain OCT, along with data regarding intraocular pressure-lowering drugs and glaucoma surgery.

Methods

Myopic atrophic maculopathy (MAM) was graded according to the ATN classification system. The presence of myopic staphyloma followed Curtin’s classification. The development of myopic neovascular maculopathy (MNM) and myopic tractional maculopathy (MTM) was also assessed, along with the presence of dome-shaped macula (DSM) and lacquer cracks (LCs) at baseline.

Main Outcome Measures

The rate of MAM progression and visual outcomes. The secondary outcome included the correlation with the presence of staphyloma subtypes and the development of MNM and MTM.

Results

The mean AXL was 31.6 ± 2.8 mm. Myopic atrophic maculopathy progressed in 57% of eyes over a mean follow-up of 11.4 years. Eyes with patchy atrophy progressed in 81% of cases, and 47% of them developed macular atrophy, whereas eyes with tessellated fundus progressed in only 19% of cases. The presence of a macular-involving staphyloma was associated with progression, particularly for type IX (86% rate of progression). A significant decline in BCVA (≥2 lines) was observed in 35.8% of eyes and correlated with AXL, glaucoma surgery, patchy atrophy, MNM, and MTM development (all P < 0.05). Active MNM developed in 190 eyes (15%), significantly associated with baseline LCs (odds ratio [OR], 2.56) and DSM (OR, 4.95), determined faster progression toward macular atrophy (OR, 5.91). Myopic tractional maculopathy complications were observed in 314 eyes (26%) and significantly correlated with the presence of a type I and II staphyloma.

Conclusions

More than half of eyes with myopic maculopathy tended to progress, in particular in cases with patchy atrophy at baseline and in eyes developing MNM or MTM, which caused worse vision loss during the study period. Although DSM and LCs correlated with neovascular complications, the shape of the posterior staphyloma correlated with tractional complications.

Financial Disclosure(s)

The authors have no proprietary or commercial interest in any materials discussed in this article.
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在一项欧洲队列的长期随访中,近视黄斑病变的纵向进展:影像学特征和视力结果。
目的:评价欧洲高度近视患者近视黄斑病变的纵向进展,分析疾病的自然病史及其对视觉功能的影响。设计:回顾性、观察性单中心队列研究。研究对象:该研究包括781名高度近视患者的1228只眼睛,随访时间至少为5年。我们收集了最佳矫正视力(BCVA)测量值、眼轴长度(AXL)、眼底摄影和光谱域光学相干断层扫描(SD-OCT),以及有关降眼压药物和青光眼手术的数据。方法:根据ATN分级系统对近视萎缩性黄斑病变(MAM)进行分级。根据科廷分级,出现近视葡萄瘤。还评估了近视黄斑新生血管(MNM)和近视牵引性黄斑病变(MTM)的发展,以及基线时圆顶状黄斑(DSM)和漆裂纹(lc)的存在。主要观察指标:MAM进展率和视力。次要结局包括与葡萄肿亚型的存在以及MNM和MTM发展的相关性。结果:平均AXL为31.6±2.8 mm。在平均11.4年的随访中,57%的眼睛出现MAM进展。斑状萎缩的眼睛在81%的病例中进展,其中47%发生黄斑萎缩,而镶嵌状眼底的眼睛仅在19%的病例中进展。累及黄斑的葡萄肿与进展有关,特别是IX型(86%的进展率)。35.8%的眼睛BCVA显著下降(≥2行),且与AXL、青光眼手术、斑状萎缩、MNM和MTM发展相关(均为)。结论:半数以上的近视黄斑病变有进展趋势,尤其是基线时出现斑状萎缩的眼睛和发生MNM或MTM的眼睛,在研究期间造成更严重的视力丧失。DSM和LCs与新生血管并发症相关,后葡萄肿的形状与牵拉并发症相关。
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来源期刊
Ophthalmology. Retina
Ophthalmology. Retina Medicine-Ophthalmology
CiteScore
7.80
自引率
6.70%
发文量
274
审稿时长
33 days
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