Diagnostic Capability of OCTA-Derived Macular Biomarkers for Early to Moderate Primary Open Angle Glaucoma

Author:

Verticchio Vercellin Alice1,Harris Alon1,Oddone Francesco2,Carnevale Carmela2ORCID,Siesky Brent A.1,Arciero Julia3,Fry Brendan4ORCID,Eckert George5ORCID,Sidoti Paul A.16ORCID,Antman Gal178ORCID,Alabi Denise1,Coleman-Belin Janet C.1ORCID,Pasquale Louis R.1

Affiliation:

1. Department of Ophthalmology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA

2. Glaucoma Unit, IRCCS—Fondazione Bietti, 00198 Rome, Italy

3. Department of Mathematical Sciences, Indiana University Indianapolis, Indianapolis, IN 46202, USA

4. Department of Mathematics and Statistics, Metropolitan State University of Denver, Denver, CO 80204, USA

5. Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN 46202, USA

6. New York Eye and Ear Infirmary of Mount Sinai, New York, NY 10003, USA

7. Department of Ophthalmology, Rabin Medical Center, Petach Tikwa 4941492, Israel

8. Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, Israel

Abstract

Background/Objectives: To investigate macular vascular biomarkers for the detection of primary open-angle glaucoma (POAG). Methods: A total of 56 POAG patients and 94 non-glaucomatous controls underwent optical coherence tomography angiography (OCTA) assessment of macular vessel density (VD) in the superficial (SCP), and deep (DCP) capillary plexus, foveal avascular zone (FAZ) area, perimeter, VD, choriocapillaris and outer retina flow area. POAG patients were classified for severity based on the Glaucoma Staging System 2 of Brusini. ANCOVA comparisons adjusted for age, sex, race, hypertension, diabetes, and areas under the receiver operating characteristic curves (AUCs) for POAG/control differentiation were compared using the DeLong method. Results: Global, hemispheric, and quadrant SCP VD was significantly lower in POAG patients in the whole image, parafovea, and perifovea (p < 0.001). No significant differences were found between POAG and controls for DCP VD, FAZ parameters, and the retinal and choriocapillaris flow area (p > 0.05). SCP VD in the whole image and perifovea were significantly lower in POAG patients in stage 2 than stage 0 (p < 0.001). The AUCs of SCP VD in the whole image (0.86) and perifovea (0.84) were significantly higher than the AUCs of all DCP VD (p < 0.05), FAZ parameters (p < 0.001), and retinal (p < 0.001) and choriocapillaris flow areas (p < 0.05). Whole image SCP VD was similar to the AUC of the global retinal nerve fiber layer (RNFL) (AUC = 0.89, p = 0.53) and ganglion cell complex (GCC) thickness (AUC = 0.83, p = 0.42). Conclusions: SCP VD is lower with increasing functional damage in POAG patients. The AUC for SCP VD was similar to RNFL and GCC using clinical diagnosis as the reference standard.

Funder

NIH

NYEE Foundation grant

Research to Prevent Blindness, NY

NSF

The Glaucoma Foundation

NEI

Publisher

MDPI AG

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