May 2008
Volume 49, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2008
Color Autofluorescence Imaging in Age-Related Macular Degeneration and Diabetic Retinopathy
Author Affiliations & Notes
  • M. Hammer
    Dept of Ophthalmology, University of Jena, Jena, Germany
  • C. Framme
    Dept of Ophthalmology, University of Regensburg, Regensburg, Germany
  • D. Schweitzer
    Dept of Ophthalmology, University of Jena, Jena, Germany
  • J. Dawczynski
    Dept of Ophthalmology, University of Jena, Jena, Germany
  • C. Liebermann
    Dept of Ophthalmology, University of Jena, Jena, Germany
  • T. Ach
    Dept of Ophthalmology, University of Jena, Jena, Germany
  • G. Schuch
    Dept of Ophthalmology, University of Regensburg, Regensburg, Germany
  • J. Strobel
    Dept of Ophthalmology, University of Jena, Jena, Germany
  • Footnotes
    Commercial Relationships  M. Hammer, None; C. Framme, None; D. Schweitzer, None; J. Dawczynski, None; C. Liebermann, None; T. Ach, None; G. Schuch, None; J. Strobel, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science May 2008, Vol.49, 4207. doi:
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      M. Hammer, C. Framme, D. Schweitzer, J. Dawczynski, C. Liebermann, T. Ach, G. Schuch, J. Strobel; Color Autofluorescence Imaging in Age-Related Macular Degeneration and Diabetic Retinopathy. Invest. Ophthalmol. Vis. Sci. 2008;49(13):4207.

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

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Abstract
 
Purpose:
 

To distinguish fluorophores at the human ocular fundus by their different emission spectra.

 
Methods:
 

Autofluorescence images were taken from 62 eyes (78.3±6.3 years) with age-related macular degeneration (AMD), 65 eyes (71.2±8.4 years) with diabetic retinopathy (RD), and 19 eyes (60.7±18.3 years) without any ophthalmic or systemic pathology (control group) by a fundus camera. All eyes were pseudophacic. A 3-chip color CCD camera was used as detector, recording the fluorescence in two separate spectral bands: Upon excitation at 475-515 nm, fluorescence was observed at 530-570 nm and 570-675 nm. For a global estimation of the fluorescence characteristics, the ratio of the green vs. the red emission (g/r) was calculated in a 70 by 70 pixel area temporal to the macula and apart from pathologic lesions and retinal vessels. Local changes of fluorescence emission spectra were assessed.

 
Results:
 

An orange fluorescence was found in the control group. Compared to that group (g/r=0.869±0.073), the global fundus fluorescence of AMD-patients (g/r=0.906±0.105) and diabetics (g/r=0.974±0.119) was green-shifted. This shift was statistically significant (t-test, p=0.001) for the RD and the control group. The optic disc, hypo-fluorescent atrophic areas (geographic atrophy, laser scars), hyper-fluorescent drusen, and lipid exudates appeared greenish (figure: normal fundus (a), AMD (b: central RPE atrophy, drusen, d: pigment abnormalities), severe non-proliferative RD (c)).

 
Conclusions:
 

The ocular fundus autofluorescence is dominated by the orange fluorescence of lipofuscin. The green-shift of the fluorescence in AMD and RD may indicate protein glycation since advanced glycation end products show green fluorescence. In the optic disc and atrophic lesions the green fluorescence of collagen is seen. Greenish fluorescence of drusen and exudates reveal non-lipofuscin fluorescence which needs further clarification. Color autofluorescence visualizes different fluorophores and, thus, may have diagnostic impact.  

 
Keywords: imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • age-related macular degeneration • diabetic retinopathy 
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