Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years.

Duncan, Jacque L; Cheng, Peiyao; Maguire, Maureen G; Ayala, Allison A; Birch, David G; Cheetham, Janet K; Durham, Todd A; Fahim, Abigail T et al. · Am J Ophthalmol · 2023

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Abstract

To evaluate disease progression using static perimetry (SP) in patients with USH2A-related retinal degeneration, including Usher syndrome type 2 (USH2) and nonsyndromic autosomal recessive retinitis pigmentosa. Prospective, observational cohort study. A total of 102 patients with biallelic disease-causing sequence variants in USH2A with baseline best-corrected visual acuity (BCVA) letter score ≥54 were recruited from 16 clinical sites in Europe and North America. SP, BCVA, full-field stimulus thresholds, spectral domain optical coherence tomography macular scans, and fundus-guided mesopic microperimetry were performed at baseline and annually. The main outcome measures were total hill of vision (V<sub>TOT</sub>), hill of vision in the central 30° (V<sub>30</sub>), V<sub>TOT</sub> minus V<sub>30</sub> (V<sub>PERIPH</sub>), and mean sensitivity. The average decline (95% CI) was 2.05 (1.40, 2.70) decibel-steradian (dB-sr)/y for V<sub>TOT</sub>, 0.48 (0.32, 0.65) dB-sr/y for V<sub>30</sub>, 1.53 (0.97, 2.08) dB-sr/y for V<sub>PERIPH</sub>, and 0.55 (0.40, 0.71) dB/y for mean sensitivity. Average percentage decline per year was 8.3 (5.5, 11.1) for V<sub>TOT</sub>, 5.2 (3.0, 7.4) for V<sub>30</sub>, 16.0 (9.5, 22.0) for V<sub>PERIPH</sub>, and 5.1 (3.5, 6.7) for mean sensitivity. Changes from baseline to year 2 in all SP measures were highly correlated (r's ranging from 0.52 [V<sub>30</sub> vs V<sub>PERIPH</sub>] to 0.98 [V<sub>TOT</sub> vs V<sub>PERIPH</sub>]). Quantitative measures of SP declined significantly over 2 years in USH2A-related retinal degeneration. The annual percentage rate of change was greatest for V<sub>TOT</sub> and V<sub>PERIPH</sub>, whereas V<sub>30</sub> and mean sensitivity changed least, reflecting earlier and more severe peripheral degeneration compared with central loss.

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