Adaptive optics imaging in inherited retinal diseases: A scoping review of the clinical literature

Surv Ophthalmol. 2024 Jan-Feb;69(1):51-66. doi: 10.1016/j.survophthal.2023.09.006. Epub 2023 Sep 29.

Abstract

Adaptive optics (AO) imaging enables direct, objective assessments of retinal cells. Applications of AO show great promise in advancing our understanding of the etiology of inherited retinal disease (IRDs) and discovering new imaging biomarkers. This scoping review systematically identifies and summarizes clinical studies evaluating AO imaging in IRDs. Ovid MEDLINE and EMBASE were searched on February 6, 2023. Studies describing AO imaging in monogenic IRDs were included. Study screening and data extraction were performed by 2 reviewers independently. This review presents (1) a broad overview of the dominant areas of research; (2) a summary of IRD characteristics revealed by AO imaging; and (3) a discussion of methodological considerations relating to AO imaging in IRDs. From 140 studies with AO outcomes, including 2 following subretinal gene therapy treatments, 75% included fewer than 10 participants with AO imaging data. Of 100 studies that included participants' genetic diagnoses, the most common IRD genes with AO outcomes are CNGA3, CNGB3, CHM, USH2A, and ABCA4. Confocal reflectance AO scanning laser ophthalmoscopy was the most reported imaging modality, followed by flood-illuminated AO and split-detector AO. The most common outcome was cone density, reported quantitatively in 56% of studies. Future research areas include guidelines to reduce variability in the reporting of AO methodology and a focus on functional AO techniques to guide the development of therapeutic interventions.

Keywords: AO-SLO; Adaptive optics; Inherited retinal diseases; Retinal dystrophy; Retinal imaging; Retinitis pigmentosa; Scoping review.

Publication types

  • Review

MeSH terms

  • ATP-Binding Cassette Transporters
  • Humans
  • Ophthalmoscopy / methods
  • Retina / diagnostic imaging
  • Retinal Cone Photoreceptor Cells
  • Retinal Diseases* / diagnostic imaging
  • Retinal Diseases* / genetics
  • Usher Syndromes*

Substances

  • ABCA4 protein, human
  • ATP-Binding Cassette Transporters