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非新生血管性年龄相关性黄斑变性的地理萎缩途径。

PATHWAYS TO GEOGRAPHIC ATROPHY IN NONNEOVASCULAR AGE-RELATED MACULAR DEGENERATION.

机构信息

Vitreous, Retina, Macula Consultants of New York, New York, New York.

出版信息

Retina. 2024 Oct 1;44(10):1655-1665. doi: 10.1097/IAE.0000000000004242.

Abstract

PURPOSE

To characterize and quantify the precursor lesions of geographic atrophy in eyes with age-related macular degeneration.

METHODS

A retrospective study of eyes with a minimum of 6-month follow-up before developing geographic atrophy. Evaluations included color and autofluorescence imaging, along with spectral-domain optical coherence tomography, employing definitions from the Consensus of Atrophy Meeting Group and Consensus on Neovascular Age-Related Macular Degeneration Nomenclature Study Group.

RESULTS

There were 55 eyes of 44 patients, who had a mean age of 81.3 years at onset of atrophy; 35 (63.6%) were female. The mean duration of follow-up before and after the advent of geographic atrophy was 4.9 years and 1.2 years, respectively. Geographic atrophy was preceded by collapse of a druse in 41 eyes (74.5%). Of these, 29 (70.7%) were drusenoid pigment epithelial detachments. Among the eyes with regressing drusen, there were 9 with overlying vitelliform deposit, and all had concurrent subretinal drusenoid deposit; however, 19 of 30 eyes with no vitelliform deposit overlying the druse had concurrent subretinal drusenoid deposit, a difference that was significant ( P < 0.001). Regression of subretinal drusenoid deposit was found in 4 eyes (7.3%), regression of vitelliform deposit associated with subretinal drusenoid deposit in 5 (9.1%), and regression of vitelliform deposit in eyes concurrently harboring drusen was found in 3 (5.4%) and regression of vitelliform deposit alone in 2 (3.6%) at the site of eventual development of geographic atrophy.

CONCLUSION

Geographic atrophy appears to develop from multiple pathways as manifested by the many precursor lesions, all various forms of extracellular deposit, that upon regression, result in a common end-stage appearance.

摘要

目的

描述并量化与年龄相关的黄斑变性患者中地图样萎缩的前期病变。

方法

对至少有 6 个月的随访时间,然后才出现地图样萎缩的眼睛进行回顾性研究。评估包括彩色和自发荧光成像,以及频域光相干断层扫描,采用来自萎缩会议组共识和新生血管性年龄相关性黄斑变性命名研究组共识的定义。

结果

有 44 名患者的 55 只眼,在萎缩开始时的平均年龄为 81.3 岁;35 只眼(63.6%)为女性。在出现地图样萎缩之前和之后的平均随访时间分别为 4.9 年和 1.2 年。41 只眼(74.5%)的地图样萎缩是由玻璃膜疣塌陷引起的。其中 29 只眼(70.7%)为玻璃膜疣性色素上皮脱离。在退行性玻璃膜疣中,有 9 只眼有上方的类脂性玻璃膜疣,所有这些眼均伴有伴发性脉络膜玻璃膜疣样沉积;然而,在 30 只没有上方类脂性玻璃膜疣的眼中,有 19 只伴有伴发性脉络膜玻璃膜疣样沉积,差异具有统计学意义(P<0.001)。在 4 只眼(7.3%)中发现脉络膜玻璃膜疣样沉积的退行性改变,在 5 只眼(9.1%)中发现与脉络膜玻璃膜疣样沉积相关的类脂性玻璃膜疣退行性改变,在 3 只眼(5.4%)中发现伴发性玻璃膜疣退行性改变,在 2 只眼(3.6%)中发现单纯类脂性玻璃膜疣退行性改变,这些都是在最终发展为地图样萎缩的部位。

结论

地图样萎缩似乎有多种途径发展,表现为多种前期病变,所有这些病变都是不同形式的细胞外沉积物,在退行性变后,导致了共同的终末期表现。

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