Natural History of Microperimetry and Optical Coherence Tomography in USH2A-Retinopathy: A Structure-Function Association Study.
prospective_cohort · Level II
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- Record sourced from PubMed, PMID 40324556.
- Also identified by DOI 10.1016/j.ajo.2025.04.034 and PMC identifier 13102027.
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Abstract
To describe the natural history of optical coherence tomography (OCT) and mesopic microperimetry (MP) parameters in the Rate of Progression of USH2A-related Retinal Degeneration (RUSH2A) study. Multicenter, international, prospective, longitudinal natural history study. Study Population: 105 participants with biallelic disease-causing variants in USH2A with a clinical diagnosis of Usher Syndrome or autosomal recessive retinitis pigmentosa who underwent annual testing over 4 years. Ellipsoid zone (EZ) area and central sub-field thickness (CST) on OCT. Mean sensitivity (MS) and mean pointwise sensitivity at predefined functional transition points (MS<sub>FTP</sub>) on MP. A total of 101 and 94 participants met criteria for OCT and MP analysis, respectively. The average EZ area was 3.9 ± 5.3 mm<sup>2</sup> at baseline which decreased to 3.3 ± 4.1 mm<sup>2</sup> at 4 years (rate of change [ROC] [-0.18 mm<sup>2</sup>/year]). The average CST decreased from 249.7 ± 35.6 to 244.1 ± 39.3 microns over 4 years (-2.14 microns/year). The average MP MS declined from 6.0 ± 5.1 dB (baseline) to 4.5 ± 4.2 (4 years) (-0.39 dB/year). The MS<sub>FTP</sub> significantly decreased over time (17.9 dB [baseline] to 10.8 dB [4 years]). Notably, at 4 years, there was a meaningful decrease (≥ 7dB) in MS<sub>FTP</sub> in 46% of study eyes. This study establishes the natural history of key structural and functional parameters in USH2A-retinopathy. The MS<sub>FTP</sub> is a novel, robust parameter that showed clinically meaningful change over time and is a promising tool to monitor treatment efficacy in clinical trials.
Medical subject headings
- Tomography, Optical Coherence
- Visual Field Tests
- Visual Fields
- Usher Syndromes
- Retinitis Pigmentosa
- Extracellular Matrix Proteins
- Retina