Quantifying cardiac dysfunction and valvular heart disease associated with subretinal drusenoid deposits in age-related macular degeneration

Author:

Fei Yang1ORCID,Jo Jason J1,Chen Sophie1,Ledesma-Gil Gerardo2,Otero-Marquez Oscar3ORCID,Mordechaev Emanuel1,Le Brandon1,Tong Yuehong3,Tai Katy1,Lema Gareth4,Rosen Richard B1,Agarwal Vikram Vedprakash5,Smith Roland Theodore35ORCID

Affiliation:

1. Ophthalmology, New York Eye and Ear Infirmary of Mount Sinai, New York, NY, USA

2. Retina Department, Institute of Ophthalmology Fundación Conde de Valenciana, Mexico, Mexico

3. New York Eye and Ear Infirmary of Mount Sinai, New York, NY, USA

4. Vitreoretinal Surgery, New York Eye and Ear Infirmary of Mount Sinai, New York, NY, USA

5. Icahn School of Medicine at Mount Sinai, New York, NY, USA

Abstract

Background/Aims Demonstrate through objective multidisciplinary imaging that subretinal drusenoid deposits (SDDs) in age-related macular degeneration (AMD) are linked to both coexistent valvular heart disease (VHD) and reduced systemic perfusion via cardiac index (CI). Methods Post-hoc analysis of cross-sectional study. 200 intermediate AMD (iAMD) subjects were assigned by masked readers to two groups: SDD (with or without drusen) and drusen (only) based on multimodal ophthalmic imaging. 65 transthoracic echocardiograms (TTEs) reports were available for cardiologist evaluation of VHD severity of the four cardiac valves and the presences of precursor lesions of aortic sclerosis (ASc) and mitral annular calcification (MAC). Necessary parameters to calculate CI were also obtained. Univariate testing was performed using Fisher's Exact test and t-test. Results 82.6% (19/23) of the iAMD subjects with at least one moderate/severe VHD had concurrent SDDs ( p = 0.0040). All cases of aortic regurgitation (6/6, p = 0.0370) and mitral regurgitation (13/13, p = 0.0004) were found with coexisting SDDs. Stenotic VHD was not significantly associated with SDDs, however 70.7% of subjects with ASc (29/41, p = 0.0108) and 76.0% of subjects with MAC (19/25, 0.0377) had coexisting SDDs. CI was available in 48 subjects and was significantly below normal levels in the SDD cohort (mean CI SDD 1.95 ± 0.60 L/min/m2, non-SDD 2.71 ± 0.73 L/min/m2, p = 0.0004). Conclusions Several specific VHDs have been found associated with the SDD form of AMD. Decreased systemic perfusion as measured by CI was also associated with SDDs, which supports a perfusion hypothesis of SDD pathogenesis. Further research is warranted to understand the relationship between cardiovascular disease and SDDs.

Funder

Research to Prevent Blindness

Regeneron Pharmaceuticals

Publisher

SAGE Publications

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