Loss of Peripheral Retinal Vessels in Retinitis Pigmentosa

Retinitis pigmentosa (RP) is the most common inherited retinal disease and a major cause of irreversible vision loss. The purpose of this study was to assess peripheral retinal vessels in RP.

A cross-sectional study.

Patients with RP and age-matched controls.

Using ultra-widefield fundus images, the retina was divided into 3 zones: posterior, midperiphery, and far periphery. To evaluate vascularity of the retina, the vessels were counted at the border of posterior and midperipheral zones (Z1/2) and the border of midperipheral and far peripheral zones (Z2/3).

Vessel counts at Z1/2 and Z2/3.

One hundred eighty-one eyes of 107 RP patients and 130 eyes of 84 controls were included. In the RP group, the median vessel counts at Z1/2 and Z2/3 were 8 and 3, respectively. These were strikingly lower than the control group with the median vessels of 42 and 43.5 at Z1/2 (P < 0.001) and Z2/3 (P < 0.001), respectively. Twenty-two percent of RP eyes were entirely avascular in the far periphery, and 7% were avascular in the midperiphery and far periphery. Only 5% of RP eyes had >25 vessels at Z2/3. There were significantly fewer vessels in the temporal retina at both Z1/2 (P = 0.01) and Z2/3 (P < 0.001) in RP eyes. Furthermore, eyes with visual acuity of 20/200 or worse had significantly fewer vessels at Z1/2 (P < 0.001) and Z2/3 (P < 0.001). There were no significant differences in the number of vessels at Z1/2 and 2/3 between the right and left eyes of RP patients with both eyes included in the study.

This study provides compelling evidence of substantial symmetrical peripheral retinal vascular loss in RP. This finding may aid in clinical diagnosis of the disease and have significant therapeutic implications.

The author(s) have no proprietary or commercial interest in any materials discussed in this article.