June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
Investigation on cone structure and function in a family affected by occult macular dystrophy
Author Affiliations & Notes
  • Lucia Ziccardi
    Neurophthalmology Unit, Bietti Eye Foundation IRCCS, Rome, Italy
  • Daniela Giannini
    Fondazione G.B. Bietti IRCCS, Rome, Italy
  • Giuseppe Lombardo
    CNR-IPCF Unit of Support Cosenza, University of Calabria, Rende, Italy
    Vision Engineering Italy srl, Rome, Italy
  • Sebastiano Serrao
    Fondazione G.B. Bietti IRCCS, Rome, Italy
  • Roberto Dell'Omo
    Medicine and Health Sciences, University of Molise, Campobasso, Italy
  • Annalisa Nicoletti
    MAGI Human Medical Genetics Institute, Rovereto, Italy
  • Matteo Bertelli
    MAGI Human Medical Genetics Institute, Rovereto, Italy
  • Marco Lombardo
    Fondazione G.B. Bietti IRCCS, Rome, Italy
  • Footnotes
    Commercial Relationships Lucia Ziccardi, None; Daniela Giannini, None; Giuseppe Lombardo, None; Sebastiano Serrao, None; Roberto Dell'Omo, None; Annalisa Nicoletti, None; Matteo Bertelli, None; Marco Lombardo, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 1784. doi:https://doi.org/
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Lucia Ziccardi, Daniela Giannini, Giuseppe Lombardo, Sebastiano Serrao, Roberto Dell'Omo, Annalisa Nicoletti, Matteo Bertelli, Marco Lombardo; Investigation on cone structure and function in a family affected by occult macular dystrophy . Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):1784. doi: https://doi.org/.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose: To study the structure and function of the cone photoreceptors in a young female (23 years old) harboring a missense mutation (p.Arg45Trp) of the Retinitis Pigmentosa 1 Like 1 (RP1L1) gene, over 2-years follow-up. The same genetic variant was found in two asymptomatic family members, i.e., the proband’s father and her brother.

Methods: High-resolution retinal images of the cone mosaic were obtained with a flood-illumination adaptive optics (AO) retinal camera in all family members. Best Corrected Visual acuity (BCVA), Contrast Sensitivity Function (CSF), combined scanning laser ophthalmoscope (SLO) and spectral domain-optical coherence tomography (SD-OCT) imaging, microperimetry (MP1), Goldmann visual field, full-field and multifocal electroretinography (mfERG) were also performed.<br />

Results: In the proband, BCVA (≤4/20) was almost stable in both eyes during the entire follow-up. Analysis of AO images demonstrated severe cone loss across the central 9 degrees of eccentricity with respect to controls. Adaptive optics was reliable to monitor the changes of the cone mosaic at a cellular level during follow-up. Both automated segmentation and texture analysis of SD-OCT images provided biomarkers to unveil the abnormalities of the photoreceptor layer’s integrity. The mfERG N1-P1 response amplitude densities (RADs) were severely reduced across the central 10 degrees in comparison with age-matched controls. The proband’s father had 20/20 BCVA and normal CSF in both eyes, nevertheless significant cone loss was found across the central 7 degrees of eccentricity; SD-OCT texture analysis and mfERG recordings showed abnormal values with respect to controls in the same retinal areas in both eyes. No abnormalities of the cone structure and function were found in the asymptomatic proband’s brother. Occult Macular Dystrophy (OMD) was diagnosed based on our genetic and clinical findings.<br />

Conclusions: The complementary use of en face and cross-section high-resolution retinal imaging tools allows to detect and to track pathological retinal changes with high accuracy over time. The quantitative assessment of photoreceptor survival or loss, based on AO imaging, is valuable for monitoring disease progression at a cellular level.<br />

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×