Correlation of SD-OCT features and retinal sensitivity in neovascular age-related macular degeneration

Invest Ophthalmol Vis Sci. 2012 Sep 21;53(10):6448-55. doi: 10.1167/iovs.11-9162.

Abstract

Purpose: To correlate retinal sensitivity in patients with neovascular age-related macular degeneration (AMD) with specific characteristics of retinal morphology.

Methods: Thirty eyes of 30 patients presenting with active choroidal neovascularization were examined by spectral domain optical coherence tomography (SD-OCT) and microperimetry (MP-1). Image-processing software was used to match a fundus photographic (FP) MP-1 image with an infrared+OCT SD-OCT image. Each MP test point for retinal sensitivity was positioned at the corresponding SD-OCT location, and the microperimetric results were evaluated.

Results: An intact retinal configuration was associated with a median retinal sensitivity of 15.5 dB (quartiles: 12 dB, 18 dB). The median retinal sensitivities were 0 dB (quartiles: 0 dB, 1 dB) for the neovascular complex, 4 dB (0 dB, 9 dB) for the subretinal fluid, 1 dB (0 dB, 6 dB) for the intraretinal fluid, and 0 dB (0 dB, 3 dB) for intraretinal cysts. Pigment epithelium detachment was associated with a median retinal sensitivity of 3 dB (0 dB, 8 dB), and subretinal drusen had a median value of 8 dB (5 dB, 12 dB). Deep retinal layer analyses gave low median retinal sensitivities of 0 dB (0 dB, 3 dB) for an absent retinal pigment epithelium layer and 1 dB (0 dB, 5 dB) for an absent photoreceptor layer.

Conclusions: Superimposition of morphological SD-OCT features and microperimetric retinal sensitivity allowed exact determination of the differential impact of retinal alteration on the corresponding sensitivity. Individual OCT-related indicators of neurosensory integrity were distinctly correlated with visual function. "Morphofunctional" findings could be relevant as prognostic factors and for (re)treatment decisions. (https://www.clinicaltrialsregister.eu/ number, 2006-005684-26.).

Publication types

  • Clinical Trial

MeSH terms

  • Choroidal Neovascularization / pathology*
  • Exudates and Transudates
  • Fundus Oculi
  • Humans
  • Image Processing, Computer-Assisted / methods*
  • Infrared Rays
  • Macular Degeneration / pathology*
  • Photography / methods
  • Prognosis
  • Retinal Detachment / pathology
  • Retinal Drusen / pathology
  • Severity of Illness Index*
  • Software
  • Tomography, Optical Coherence / methods*
  • Vision Tests / methods
  • Visual Acuity
  • Visual Field Tests / methods