AI Article Synopsis

  • This study investigates the patterns of preserved peripheral visual field (pVF) in patients with retinitis pigmentosa (RP), a condition that leads to vision loss, to better understand potential therapeutic targets.
  • Researchers created a computational tool to map the spatial distribution of retained pVF using data from 152 subjects, segmented by disease duration, and found that preservation is typically located in specific areas of the retina.
  • The study concludes that some retinal cells in the superonasal region may be more resilient to degeneration, suggesting that further research on these cells could help develop new treatments for RP.

Article Abstract

Purpose: Retinitis pigmentosa (RP) is typified by progressive peripheral visual field (pVF) loss in patterns that can vary between individuals. Greater understanding of pVF preservation may inform research on therapeutic targets. However, characteristics of retained pVF are incompletely understood. We aimed to evaluate the spatial characteristics of retained pVF in RP.

Methods: We developed a computational platform to generate a probability map of the spatial distribution of retained pVF loci using the Goldmann V4e isopter. RP subjects were grouped into cross-sectional and longitudinal datasets. Probability maps of retained pVF were generated for categories of symptomatic disease duration (SDD). We applied a mathematical model to determine the anatomical correlate of the retained pVF.

Results: A total of 152 subjects were included. The mean age was 46.7 years. SDD was <20 years (47.4%), 20 to 40 years (39.5%), or >40 years (13.2%). Longitudinal data (3.2-5.7 years of follow up) were available for 65 subjects. In the cross-sectional dataset, retained pVF loci were most likely to be located between the 50° and 80° isoeccentric meridians and between the 30° to 50° radial axes. In the longitudinal dataset, inferotemporal pVF loci were the most likely to be preserved over time. The area of pVF retention corresponded anatomically to the pre-equatorial superonasal retina.

Conclusions: Semiautomated quantitation of pVF may be a useful tool to analyze spatial characteristics of VF in RP. Retinal cells in the superonasal periphery may be resilient to RP-related functional decline. Understanding the cellular and molecular basis of pVF resilience in the retina may inform efforts to develop treatment modalities for RP.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857617PMC
http://dx.doi.org/10.1167/iovs.63.2.26DOI Listing

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