Recent Advances in Imaging Macular Atrophy for Late-Stage Age-Related Macular Degeneration

Author:

Cheng Anny M. S.123ORCID,Chalam Kakarla V.4ORCID,Brar Vikram S.5,Yang David T. Y.6,Bhatt Jineel2,Banoub Raphael G.12,Gupta Shailesh K.12

Affiliation:

1. Department of Ophthalmology, Broward Health, Fort Lauderdale, FL 33064, USA

2. Specialty Retina Center, Coral Springs, FL 33067, USA

3. Department of Ophthalmology, Herbert Wertheim College of Medicine, Florida International University, Miami, FL 33199, USA

4. Department of Ophthalmology, Loma Linda University, Loma Linda, CA 92350, USA

5. Department of Ophthalmology, Virginia Commonwealth University, Richmond, VA 23298, USA

6. College of Biological Science, University of California, Davis, Sacramento, CA 95616, USA

Abstract

Age-related macular degeneration (AMD) is a leading cause of blindness worldwide. In late-stage AMD, geographic atrophy (GA) of dry AMD or choroidal neovascularization (CNV) of neovascular AMD eventually results in macular atrophy (MA), leading to significant visual loss. Despite the development of innovative therapies, there are currently no established effective treatments for MA. As a result, early detection of MA is critical in identifying later central macular involvement throughout time. Accurate and early diagnosis is achieved through a combination of clinical examination and imaging techniques. Our review of the literature depicts advances in retinal imaging to identify biomarkers of progression and risk factors for late AMD. Imaging methods like fundus photography; dye-based angiography; fundus autofluorescence (FAF); near-infrared reflectance (NIR); optical coherence tomography (OCT); and optical coherence tomography angiography (OCTA) can be used to detect and monitor the progression of retinal atrophy. These evolving diverse imaging modalities optimize detection of pathologic anatomy and measurement of visual function; they may also contribute to the understanding of underlying mechanistic pathways, particularly the underlying MA changes in late AMD.

Publisher

MDPI AG

Subject

Clinical Biochemistry

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