Author/Authors :
Sabbaghi, Hamideh Ophthalmic Epidemiology Research Center - Research Institute for Ophthalmology and Vision Science - Shahid Beheshti University of Medical Sciences, Tehran, Iran - Department of Optometry - School of Rehabilitation - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Daftarian, Narsis Ocular Tissue Engineering Research Center - Research Institute for Ophthalmology and Vision Science - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Hassanpour, Kiana Ophthalmic Research Center - Research Institute for Ophthalmology and Vision Science - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Fekri, Sahba Ophthalmic Research Center - Research Institute for Ophthalmology and Vision Science - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Nourinia, Ramin Ophthalmic Research Center - Research Institute for Ophthalmology and Vision Science - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Suri, Fatemeh Ophthalmic Research Center - Research Institute for Ophthalmology and Vision Science - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Kheiri, Bahareh Ophthalmic Research Center - Research Institute for Ophthalmology and Vision Science - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Yaseri, Mehdi Department of Epidemiology and Biostatistics - Tehran University of Medical Sciences, Tehran, Iran , Rajabpour, Mojtaba Department of Optometry - School of Rehabilitation - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Sheibani, Kourosh Basir Eye Health Research Center, Tehran, Iran , Ahmadieh, Hamid Ophthalmic Research Center - Research Institute for Ophthalmology and Vision Science - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Purpose: To investigate the retinal vascular characteristics among patients with different types of inherited retinal dystrophies (IRDs).
Methods: This comparative cross‑sectional study was conducted on 59 genetically confirmed cases of IRD including 37 patients with retinitis
pigmentosa (RP) (74 eyes), 13 patients with Stargardt disease (STGD) (26 eyes), and 9 patients with cone‑rod dystrophy (CRD) (18 eyes). Both
eyes of 50 age‑ and sex‑matched healthy individuals were investigated as controls. All participants underwent optical coherence tomography
angiography to investigate the vascular densities (VDs) of superficial and deep capillary plexus (SCP and DCP) as well as foveal avascular zone area.
Results: In RP, significantly lower VD in whole image (P = 0.001 for DCP), fovea (P = 0.038 for SCP), parafovea (P < 0.001 for SCP and
DCP), and perifovea (P < 0.001 for SCP and DCP) was observed compared to controls. In STGD, VD of parafovea (P = 0.012 for SCP
and P = 0.001 for DCP) and fovea (P = 0.016 for DCP) was significantly lower than controls. In CRD, the VD of parafovea (P = 0.025 for
DCP) was significantly lower than controls. Whole image density was significantly lower in RP compared to STGD (P < 0.001 for SCP) and
CRD (P = 0.037 for SCP). VD in parafovea (P = 0.005 for SCP) and perifovea (P < 0.001 for SCP and DCP) regions was significantly lower
in RP compared with STGD. Also, foveal VD in STGD was significantly lower than RP (P = 0.023 for DCP).
Conclusion: Our study demonstrated lower VDs in three different IRDs including RP, STGD, and CRD compared to healthy controls. Changes
were more dominant in RP patients.
Keywords :
Inherited retinal dystrophies , Optical coherence tomography angiography , Retinal vascular abnormalities , Vessel density , Retinitis pigmentosa , Stargardt disease , Cone‑rod dystrophy
