April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Drusen volume progression and the Development of neovascular Age-related Macular Degeneration
Author Affiliations & Notes
  • Ferdinand Georg Schlanitz
    Ophthalmology, Medical University of Vienna, Vienna, Austria
  • Bernhard Baumann
    Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria
  • Alessio Montuoro
    Vienna Reading Center, Department of Ophthalmology, Medical University of Vienna, Vienna, Austria
  • Ulrike Scheschy
    Ophthalmology, Medical University of Vienna, Vienna, Austria
  • Abtin Shahlaee
    Ophthalmology, Medical University of Vienna, Vienna, Austria
  • Magdalena Baratsits
    Ophthalmology, Medical University of Vienna, Vienna, Austria
  • Tamara J Mittermüller
    Ophthalmology, Medical University of Vienna, Vienna, Austria
  • Michael Pircher
    Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria
  • Christoph K Hitzenberger
    Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria
  • Ursula Schmidt-Erfurth
    Ophthalmology, Medical University of Vienna, Vienna, Austria
  • Footnotes
    Commercial Relationships Ferdinand Schlanitz, None; Bernhard Baumann, Canon (F); Alessio Montuoro, None; Ulrike Scheschy, None; Abtin Shahlaee, None; Magdalena Baratsits, None; Tamara Mittermüller, None; Michael Pircher, Canon (C), Canon (F); Christoph Hitzenberger, Canon (C), Canon (F); Ursula Schmidt-Erfurth, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 3530. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Ferdinand Georg Schlanitz, Bernhard Baumann, Alessio Montuoro, Ulrike Scheschy, Abtin Shahlaee, Magdalena Baratsits, Tamara J Mittermüller, Michael Pircher, Christoph K Hitzenberger, Ursula Schmidt-Erfurth; Drusen volume progression and the Development of neovascular Age-related Macular Degeneration. Invest. Ophthalmol. Vis. Sci. 2014;55(13):3530.

      Download citation file:


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

      ×
  • Supplements
Abstract
 
Purpose
 

To identify the pathway from drusen progression to the development of advanced age-related macular degeneration (AMD).

 
Methods
 

Patients with early AMD were imaged using simultaneous spectral-domain (SD-OCT, Spectralis) and polarization-sensitive OCT (PS-OCT). All patients underwent continuous follow-up examinations every 6 months for three years. Data obtained with PS-OCT were segmented for drusen volume automatically using an algorithm based on the RPE-based polarization-sensitive information, whereas SD-OCT data were segmented manually by expert graders using an OCT-reader software (OCTAVO).

 
Results
 

104 patients were enclosed in the study. Out of this group, 56 eyes with very good scanning quality and continuous follow-up visits were selected for manual grading. In total, more than 32000 individual B-scans were graded and compared to the results of the automated segmentation done by PS-OCT. The mean drusen volume per eye at baseline was 0.12mm3 for SD-OCT and 0.15mm3 for PS-OCT. The increase of drusen volume over time was shown to be approximately linear, with a regression equation of y=0.028x + 1.0 for SD-OCT and y=0.029x + 1.0 for PS-OCT (x = months), with a calculated doubling of drusen volume after 35.1 resp. 34.2 months. Drusen regression was observed in 28 eyes at least once over three years. Of this group, 8 eyes developed choroidal neovascularization (CNV) and 2 eyes geographic atrophy. Eyes without drusen regression showed no signs of progression towards advanced AMD.

 
Conclusions
 

Drusen showed a linear increase in volume over time. A spontaneous regression without signs of advanced AMD occurred quite often. However, the development of advanced AMD was announced by a regression of drusen volume. Therefore, OCT showed to be a promising tool for predicting the individual risk for progression of AMD.

  
Keywords: 504 drusen • 412 age-related macular degeneration • 550 imaging/image analysis: clinical  
×
×

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.

×