June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
One-year macular volume change of the neurosensory retina in intermediate AMD by SDOCT semi-automated segmentation
Author Affiliations & Notes
  • Eric Yuan
    Ophthalmology, Duke University, Durham, NC
  • Francisco Folgar
    Ophthalmology, Duke University, Durham, NC
  • Stephanie Chiu
    Biomedical Engineering, Duke University, Durham, NC
  • Sina Farsiu
    Ophthalmology, Duke University, Durham, NC
    Biomedical Engineering, Duke University, Durham, NC
  • Cynthia Toth
    Ophthalmology, Duke University, Durham, NC
    Biomedical Engineering, Duke University, Durham, NC
  • Footnotes
    Commercial Relationships Eric Yuan, None; Francisco Folgar, None; Stephanie Chiu, Duke University (P); Sina Farsiu, Duke University (P); Cynthia Toth, Genentech (F), Bioptigen (F), Physical Sciences Inc. (F), Unlicensed (P)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 6293. doi:
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    • Get Citation

      Eric Yuan, Francisco Folgar, Stephanie Chiu, Sina Farsiu, Cynthia Toth; One-year macular volume change of the neurosensory retina in intermediate AMD by SDOCT semi-automated segmentation. Invest. Ophthalmol. Vis. Sci. 2013;54(15):6293.

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

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Abstract
 
Purpose
 

In non-advanced age-related macular degeneration (AMD), retinal thinning may occur over drusen, but it is unclear whether changes occur to the entire neurosensory retinal volume (NSRV) of the macula. We sought to compare NSRV of eyes with intermediate AMD vs. aged control eyes, and to correlate NSRV with future AMD progression.

 
Methods
 

Spectral domain optical coherence tomography (SDOCT) was obtained in 314 AMD eyes and 122 control eyes enrolled in the prospective observational AREDS2 Ancillary SDOCT Study. Semi-automated SDOCT segmentation of the neurosensory retina was performed from internal limiting membrane to outer border of the photoreceptor layer within a 5-mm diameter field centered on the fovea. Complete SDOCT segmentation and NSRV calculation were achieved in 269 AMD eyes and 118 control eyes at baseline. NSRV was compared between AMD and control eyes, and NSRV change was compared between baseline and year 1. In AMD eyes with noncentral geographic atrophy (GA), baseline NSRV was correlated to color fundus photography (CFP) measurement of GA area at years 2 and 4 of follow-up.

 
Results
 

Baseline NSRV (mean ± standard deviation) was 5.21 ±0.42 mm3 for 269 AMD eyes and 5.06 ±0.35 mm3 for 118 controls (p<0.001). Year 1 NSRV was 5.16 ±0.37 mm3 for 250 AMD eyes and 5.02 ±0.32 mm3 for 99 controls (p<0.001). In paired baseline and year 1 scans, NSRV decreased significantly for AMD (-0.05 ±0.15 mm3, p<0.001) and controls (-0.03 ±0.06 mm3, p<0.001). There was no significant difference between AMD and controls for NSRV change (p=0.15) or percent of eyes with decreased NSRV (70% AMD vs. 74% controls, p=0.59) from baseline to year 1. In eyes with noncentral GA based on CFP measurement, smaller baseline NSRV was correlated with greater total GA area at year 2 (n=23 eyes, Spearman rho=-0.76 p<0.001), greater total GA area at year 4 (n=30 eyes, Spearman rho=-0.52, p=0.003), and greater change in GA area from baseline to year 4 (Spearman rho=-0.54, p=0.003).

 
Conclusions
 

Total macular volume of the neurosensory retina was greater in eyes with intermediate AMD than controls, but the volume decreased in both groups over 1 year. Structural or inflammatory changes may induce macular thickening in some early categories of AMD. In intermediate AMD, NSRV was negatively correlated with future GA area; therefore, NSRV may serve as an SDOCT biomarker that predicts progression of GA size.

 
Keywords: 688 retina  
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