High-resolution imaging of photoreceptors in macular microholes

Invest Ophthalmol Vis Sci. 2014 Aug 21;55(9):5932-43. doi: 10.1167/iovs.13-13792.

Abstract

Purpose: To assess photoreceptor structure in macular microholes by using adaptive optics scanning laser ophthalmoscopy (AO-SLO) and spectral-domain optical coherence tomography (SD-OCT) and compare with visual acuity.

Methods: Fourteen eyes from 12 patients with macular microholes underwent a full ophthalmologic examination and imaging with a fundus camera, SD-OCT, and an original prototype AO-SLO system at each visit.

Results: All eyes had a cone outer segment tip line disruption and a normal retinal pigment epithelium line on SD-OCT images. Adaptive optics scanning laser ophthalmoscopy revealed foveal cone disruption (13 eyes, round or oval; 1 eye, T-shaped) in all eyes. Cone disruption area (mean = 14,805 ± 9120 μm(2); range, 3495-35,901 μm(2)) positively correlated with logMAR visual acuity at the first visit (P = 0.015, rs = 0.679). During the follow-up period, cone disruption area increased in two eyes, was stable in seven eyes, and decreased in five eyes. At the last visit, cone disruption area (mean = 8717 ± 7432 μm(2); range, 0-25,746 μm(2)) also positively correlated with logMAR visual acuity (P = 0.035, rs = 0.610). In one patient with bilateral microholes and no apparent vitreous traction, lesion size gradually increased. Cone disruption area decreased and visual acuity improved following oral prednisone therapy.

Conclusions: Cone disruption occurs in eyes with macular microholes and a larger cone disruption area translates into a poorer visual acuity. Macular microholes, which are commonly observed as foveal cone inner and outer segment disruptions, may occur in eyes with or without vitreofoveal traction.

Keywords: adaptive optics; macular microhole; optical coherence tomography; scanning laser ophthalmoscopy.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Female
  • Fovea Centralis / pathology
  • Humans
  • Male
  • Middle Aged
  • Retinal Cone Photoreceptor Cells / pathology*
  • Retinal Perforations / pathology*
  • Scotoma / pathology
  • Tomography, Optical Coherence / instrumentation*
  • Tomography, Optical Coherence / methods*
  • Visual Acuity
  • Vitreous Body / pathology*