Arnal Leo, Mesfin Yeabsira, Xu Christine, Salvi Anish, Mishra Kapil, Ludwig Chase A
Byers Eye Institute, Stanford University School of Medicine.
University of California, San Francisco School of Medicine.
Res Sq. 2025 Aug 18:rs.3.rs-7329335. doi: 10.21203/rs.3.rs-7329335/v1.
As myopia reaches epidemic levels worldwide, its role in driving vision-threatening retinal complications is increasingly urgent. This study quantifies the burden of myopia by examining its association with key retinal diseases and how risk escalates with increasing severity.
We conducted a retrospective cohort study using the STARR clinical data warehouse, including all patients with ≥1 documented eye visit. Myopia severity was defined by spherical equivalent and axial length, classifying patients as non-myopic, myopic, highly myopic, or severely myopic. Primary outcomes included six retinal diseases associated with myopia: choroidal neovascularization (CNV), myopic macular degeneration (MMD), foveoschisis, macular hole (MH), rhegmatogenous retinal detachment (RRD), and foveal retinal detachment (FRD). Adjusted logistic regression estimated odds by myopia severity and spherical equivalent. Mean age at diagnosis was compared across groups.
Retinal complications occurred at younger ages with increasing myopia severity. Compared to non-myopes, myopic, highly myopic, and severely myopic patients had 2.45 (95% CI: 2.36-2.55), 2.46 (95% CI: 2.31-2.62), and 8.15 (95% CI: 7.17-9.27) times higher odds, respectively, of developing any retinal complication. Per diopter increase in myopia, the odds of each complication increased: CNV (OR 1.11; 95% CI: 1.09-1.12), MMD (OR 1.22; 95% CI: 1.18-1.25), foveoschisis (OR 1.22; 95% CI: 1.16-1.28), MH (OR 1.06; 95% CI: 1.05-1.08), FRD (OR 1.23; 95% CI: 1.16-1.32), and RRD (OR 1.10; 95% CI: 1.10-1.11). In severe myopes, odds were markedly elevated: CNV (OR 22.90), MMD (OR 60.19), foveoschisis (OR 102.98), MH (OR 6.69), FRD (OR 22.72), and RRD (OR 6.84).
Myopia is independently associated with higher odds of retinal diseases, and this risk increases incrementally with severity. These findings support a dose-response relationship and highlight the importance of early risk stratification, tailored monitoring, and timely referral in patients with high and severe myopia.
随着近视在全球范围内达到流行程度,其在引发威胁视力的视网膜并发症方面的作用日益紧迫。本研究通过考察近视与关键视网膜疾病的关联以及风险如何随严重程度增加而升高,对近视负担进行了量化。
我们利用STARR临床数据仓库进行了一项回顾性队列研究,纳入了所有有≥1次眼科就诊记录的患者。近视严重程度由等效球镜和眼轴长度定义,将患者分为非近视、近视、高度近视或重度近视。主要结局包括六种与近视相关的视网膜疾病:脉络膜新生血管(CNV)、近视性黄斑变性(MMD)、黄斑劈裂、黄斑裂孔(MH)、孔源性视网膜脱离(RRD)和黄斑区视网膜脱离(FRD)。调整后的逻辑回归按近视严重程度和等效球镜估计比值比。比较了各组的诊断平均年龄。
视网膜并发症在较年轻的年龄出现,且随着近视严重程度增加。与非近视患者相比,近视、高度近视和重度近视患者发生任何视网膜并发症的比值比分别高2.45(95%置信区间:2.36 - 2.55)、2.46(95%置信区间:2.31 - 2.62)和8.15(95%置信区间:7.17 - 9.27)倍。近视每增加1屈光度,每种并发症的比值比均升高:CNV(比值比1.11;95%置信区间:1.09 - 1.12)、MMD(比值比1.22;95%置信区间:1.18 - 1.25)、黄斑劈裂(比值比1.22;95%置信区间:1.16 - 1.28)、MH(比值比1.06;95%置信区间:1.05 - 1.08)、FRD(比值比1.23;95%置信区间:1.16 - 1.32)和RRD(比值比1.10;95%置信区间:1.10 - 1.11)。在重度近视患者中,比值比显著升高:CNV(比值比22.90)、MMD(比值比60.19)、黄斑劈裂(比值比102.98)、MH(比值比6.69)、FRD(比值比22.72)和RRD(比值比6.84)。
近视与视网膜疾病的较高发病几率独立相关,并随着严重程度的增加而逐步升高。这些发现支持剂量反应关系,并突出了对高度近视和重度近视患者进行早期风险分层、针对性监测及及时转诊的重要性。