Quantitative Autofluorescence in Non-Neovascular Age Related Macular Degeneration

Author:

Chandra Shruti12ORCID,Grewal Manjot K.2,Gurudas Sarega1,Sondh Rajan3ORCID,Bird Alan12,Jeffery Glen1,Chong Victor1ORCID,Sivaprasad Sobha12ORCID

Affiliation:

1. Institute of Ophthalmology, University College London, London EC1V 9EL, UK

2. Moorfields National Institute of Health and Care Research Facility, Moorfields Eye Hospital, London EC1V 2PD, UK

3. Sandwell and West Birmingham Hospitals NHS Trust, Birmingham B71 4HJ, UK

Abstract

Quantitative autofluorescence (qAF8) level is a presumed surrogate marker of lipofuscin content in the retina. We investigated the changes in the qAF8 levels in non-neovascular AMD. In this prospective cohort study, Caucasians aged ≥50 years with varying severity of non-neovascular AMD in at least one eye and Snellen visual acuity ≥6/18 were recruited. The qAF8 levels were analysed in the middle eight segments of the Delori pattern (HEYEX software, Heidelberg, Germany). The AMD categories were graded using both the Beckman classification and multimodal imaging (MMI) to include the presence of subretinal drusenoid deposits (SDD). A total of 353 eyes from 231 participants were analyzed. Compared with the age-matched controls, the qAF8 values decreased in the eyes with AMD (adjusted % difference = −19.7% [95% CI −28.8%, −10.4%]; p < 0.001) and across the AMD categories, (adjusted % differences; Early, −13.1% (−24.4%, −1%), p = 0.04; intermediate AMD (iAMD), −22.9% (−32.3%, −13.1%), p < 0.001; geographic atrophy −25.2% (−38.1%, −10.4%), p = 0.002). On MMI, the qAF8 was reduced in the AMD subgroups relative to the controls, (adjusted % differences; Early, −5.8% (−18.9%, 8.3%); p = 0.40; iAMD, −26.7% (−36.2%, −15.6%); p < 0.001; SDD, −23.7% (−33.6%, −12.2%); p < 0.001; atrophy, −26.7% (−39.3%, −11.3%), p = 0.001). The qAF8 levels declined early in AMD and were not significantly different between the severity levels of non-neovascular AMD, suggesting the early and sustained loss of function of the retinal pigment epithelium in AMD.

Funder

Fight For Sight

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

Reference41 articles.

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3. An overview of the role of lipofuscin in age-related neurodegeneration;Kun;Front. Neurosci.,2018

4. Pathophysiology of age-related macular degeneration;Young;Surv. Ophthalmol.,1987

5. Autofluorescence distribution associated with drusen in age-related macular degeneration;Delori;Investig. Ophthalmol. Vis. Sci.,2000

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