Stages of Drusen-Associated Atrophy in Age-Related Macular Degeneration Visible via Histologically Validated Fundus Autofluorescence

被引:26
作者
Chen, Ling [1 ,2 ,3 ]
Messinger, Jeffrey D. [1 ]
Ferrara, Daniela [4 ]
Freund, K. Bailey [5 ,6 ,7 ,8 ]
Curcio, Christine A. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Ophthalmol & Visual Sci, Sch Med, 1670 Univ Blvd,Room 360, Birmingham, AL 35294 USA
[2] Chongqing Med Univ, Affiliated Hosp 1, Chongqing Key Lab Ophthalmol, Chongqing, Peoples R China
[3] Chongqing Eye Inst, Chongqing, Peoples R China
[4] Genentech Inc, San Francisco, CA 94080 USA
[5] Vitreous Retina Macula Consultants New York, New York, NY USA
[6] Manhattan Eye Ear & Throat Hosp, LuEsther T Mertz Retinal Res Ctr, New York, NY 10021 USA
[7] NYU, Dept Ophthalmol, Sch Med, 550 1St Ave, New York, NY 10016 USA
[8] Columbia Univ Coll Phys & Surg, Harkness Eye Inst, 630 W 168th St, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
age-related macular degeneration; autofluorescence; drusen-associated atrophy; photoreceptors; retinal pigment epithelium; RETINAL-PIGMENT EPITHELIUM; OPTICAL COHERENCE TOMOGRAPHY; NATURAL-HISTORY; LIPOFUSCIN; EYES; FLUORESCENCE; LESION;
D O I
10.1016/j.oret.2020.11.006
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To determine histologic correlates for stages of drusen-associated atrophy observed with fundus autofluorescence (FAF) and color fundus photography (CFP), of eyes with advanced age-related macular degeneration (AMD). Design: Case study and clinicopathologic correlation. Participant: A white woman with AMD findings of inactive subretinal fibrosis (right eye) and untreated nonexudative type 1 macular neovascularization (left eye) was followed for 9 years before death at 90 years of age. Methods: Eyes preserved 6.25 hours after death were postfixed in osmium tannic acid paraphenylenediamine and were prepared for submicrometer epoxy resin sections (115 and 90 from the right and left eye, respectively), with 19 aligned to clinical B-scans. Drusen visible by CFP at the last visit were assigned to 4 stages of FAF: stage 1, isoautofluorescence; stage 2, mildly uniform hyperautofluorescence; stage 3, a ring of hyperautofluorescence around a center of the hypoautofluorescence; and stage 4, uniform hypoautofluorescence. Main Outcome Measures: Light microscopic morphologic features at known FAF stages, including druse size, druse contents, and changes in overlying retinal pigment epithelium (RPE), photoreceptors, and external limiting membrane (ELM). Results: Histologic examination of 166 drusen demonstrated that stage 1 isoautofluorescent drusen were visible on CFP. Hyperautofluorescence in stage 2 corresponded to short photoreceptors and complete coverage by RPE. Hypoautofluorescence in stages 3 and 4 corresponded to different extents of RPE atrophy (RPE gap and no RPE, respectively). Of stage 4 drusen, 67% showed no outer nuclear layer (ONL) and an undetectable ELM. Stage 4 included a high proportion of refractile drusen (82%) with many calcific nodules, visible on CFP. Conclusions: We present the first direct clinicopathologic correlation for FAF imaging of drusen-associated atrophy. Our data support 4 FAF stages of drusen-associated atrophy. Stage 2 is the earliest detected stage in which loss of screening by photoreceptor photopigment contributes to uniform hyperautofluorescence. Stages 3 and 4 comport with incomplete RPE and outer retinal atrophy as defined by the Classification of Atrophy Meetings group. Loss of RPE, ONL, and ELM in stage 4 indicates that atrophy can begin over individual drusen. Findings will help the identification of new therapeutic approaches and clinical study end points. (C) 2020 by the American Academy of Ophthalmology
引用
收藏
页码:730 / 742
页数:13
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