Optical Coherence Tomography Angiography in CRB1-Associated Retinal Dystrophies

Author:

Rajabian Firuzeh1,Arrigo Alessandro1ORCID,Bianco Lorenzo1ORCID,Antropoli Alessio1ORCID,Manitto Maria Pia1,Martina Elisabetta1,Bandello Francesco1ORCID,Chhablani Jay2ORCID,Battaglia Parodi Maurizio1ORCID

Affiliation:

1. Department of Ophthalmology, Vita-Salute San Raffaele University, IRCCS Ospedale San Raffaele, 20132 Milan, Italy

2. Department of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA

Abstract

Aim of the study: To report optical coherence tomography angiography (OCTA) findings in patients affected by CRB1-associated retinal dystrophies. Method: Patients affected by a genetically confirmed CRB1-associated retinal dystrophy were prospectively enrolled in an observational study, along with age- and sex-matched healthy volunteers as control subjects. All study and control subjects received a complete ophthalmic examination and multimodal retinal imaging, including OCTA. Result: A total of 12 eyes from 6 patients were included in the study. The mean BCVA of patients was 0.42 ± 0.25 logMAR. Two patients showed large central atrophy, with corresponding definite hypo-autofluorescence on fundus autofluorescence (FAF). Another four patients disclosed different degrees of RPE mottling, with uneven FAF. On OCTA, the macular deep capillary plexus and choriocapillaris had a lower vessel density in eyes affected by CRB1-associated retinopathy when compared to healthy controls. On the other hand, vessel density at the peripapillary radial capillary plexus, superficial capillary plexus, and deep capillary plexus was significantly altered with respect to control eyes. Statistical analyses disclosed a negative correlation between the deep capillary plexus and both LogMAR best corrected visual acuity and central retinal thickness. Conclusion: Our study reveals that CRB1-associated retinal dystrophies are characterized by vascular alterations both in the macular and peripapillary region, as assessed by OCTA.

Publisher

MDPI AG

Subject

General Medicine

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