Ufa Eye Research Institute, Ufa, Russia.
Department of Ophthalmology, University Hospital Heidelberg, Heidelberg, Germany.
Invest Ophthalmol Vis Sci. 2024 Mar 5;65(3):29. doi: 10.1167/iovs.65.3.29.
To assess the prevalence of myopic macular degeneration (MMD) in very old individuals.
The population-based Ural Very Old Study (UVOS) included 1526 (81.1%) of 1882 eligible inhabitants aged ≥85 years. Assessable fundus images were available for 930 (60.9%) individuals (mean age, 88.6 ± 2.7 years). MMD was defined by macular patchy atrophies (i.e., MMD stage 3 and 4 as defined by the Pathologic Myopia Study Group).
MMD prevalence was 21 of 930 (2.3%; 95% CI, 1.3-3.3), with 10 individuals (1.1%; 95% CI, 0.4-1.7) having MMD stage 3 and 11 participants (1.2%; 95% CI, 0.5-1.9) MMD stage 4 disease. Within MMD stage 3 and 4, prevalence of binocular moderate to severe vision impairment was 4 of 10 (40%; 95% CI, 31-77) and 7 of 11 (64%; 95% CI, 30-98), respectively, and the prevalence of binocular blindness was 2 of 10 (20%; 95% CI, 0-50) and 3 of 11 (27%; 95% CI, 0-59), respectively. In minor myopia (axial length, 24.0 to <24.5 mm), moderate myopia (axial length, 24.5 to <26.5 mm), and high myopia (axial length, ≥26.5 mm), MMD prevalence in the right eyes was 0 of 46 eyes (0%), 3 of 40 eyes (8%; 95% CI, 0-16), and 7 of 9 (78%; 95% CI, 44-100), respectively; MMD prevalence in the left eyes was 1 in 48 eyes (2%; 95% CI, 0-6), 4 of 36 eyes (11%; 95% CI, 0-22), and 3 of 4 eyes (75%; 95% CI, 0-100), respectively. In multivariable analysis, a higher MMD prevalence (odds ratio, 8.89; 95% CI, 3.43-23.0; P < 0.001) and higher MMD stage (beta, 0.45; B, 19; 95% CI, 0.16-0.22; P < 0.001) were correlated with longer axial length but not with any other ocular or systemic parameter.
MMD prevalence (stages 3 and 4) in very old individuals increased 8.89-fold for each mm axial length increase, with a prevalence of ≥75% in highly myopic eyes. In old age, highly myopic individuals have a high risk of eventually developing MMD with marked vision impairment.
评估极老年人中近视性黄斑变性(MMD)的患病率。
基于人群的乌拉尔极老年人研究(UVOS)纳入了 1882 名符合条件的 85 岁以上的居民,其中 1526 名(81.1%)参与了研究。对 930 名(60.9%)可评估眼底图像的个体进行了评估(平均年龄为 88.6 ± 2.7 岁)。MMD 定义为黄斑斑片状萎缩(即病理性近视研究组定义的 MMD 3 期和 4 期)。
930 例中 MMD 的患病率为 21 例(2.3%;95%CI,1.3-3.3),其中 10 例(1.1%;95%CI,0.4-1.7)为 MMD 3 期,11 例(1.2%;95%CI,0.5-1.9)为 MMD 4 期疾病。在 MMD 3 期和 4 期中,双眼中度至重度视力损害的患病率分别为 4/10(40%;95%CI,31-77)和 7/11(64%;95%CI,30-98),双眼失明的患病率分别为 2/10(20%;95%CI,0-50)和 3/11(27%;95%CI,0-59)。在轻度近视(眼轴长度 24.0 至<24.5mm)、中度近视(眼轴长度 24.5 至<26.5mm)和高度近视(眼轴长度≥26.5mm)中,右眼 MMD 的患病率分别为 0/46 眼(0%)、3/40 眼(8%;95%CI,0-16)和 7/9 眼(78%;95%CI,44-100);左眼 MMD 的患病率分别为 1/48 眼(2%;95%CI,0-6)、4/36 眼(11%;95%CI,0-22)和 3/4 眼(75%;95%CI,0-100)。多变量分析显示,较高的 MMD 患病率(比值比,8.89;95%CI,3.43-23.0;P<0.001)和较高的 MMD 分期(β,0.45;B,19;95%CI,0.16-0.22;P<0.001)与眼轴长度的增加相关,但与任何其他眼部或全身参数无关。
极老年人中 MMD(3 期和 4 期)的患病率随眼轴长度每增加 1mm 而增加 8.89 倍,高度近视眼的患病率≥75%。在老年时期,高度近视的个体最终发生 MMD 并导致明显视力损害的风险很高。