April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Calcified Drusen: Multimodal Clinical Imaging and Histology
Author Affiliations & Notes
  • Mihoko Suzuki
    Vitreous Retina Macula Consultants of New York, New York, NY
  • Sotaro Ooto
    Vitreous Retina Macula Consultants of New York, New York, NY
  • Christine A Curcio
    Ophahtlmology, University of Alabama, Birmingham, AL
  • Richard F Spaide
    Vitreous Retina Macula Consultants of New York, New York, NY
  • Footnotes
    Commercial Relationships Mihoko Suzuki, None; Sotaro Ooto, None; Christine Curcio, None; Richard Spaide, Topcon (C)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 3526. doi:
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    • Get Citation

      Mihoko Suzuki, Sotaro Ooto, Christine A Curcio, Richard F Spaide; Calcified Drusen: Multimodal Clinical Imaging and Histology. Invest. Ophthalmol. Vis. Sci. 2014;55(13):3526.

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

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Abstract
 
Purpose
 

To investigate calcified drusen in patients with age-related macular degeneration with multimodal imaging and in donor eyes with histology.

 
Methods
 

Color fundus photographs, spectral-domain optical coherence tomography (OCT) and fundus autofluorescence (AF) imaging were obtained as part of a comprehensive ophthalmologic examination. Eyes with calcified drusen were identified by visualization of refractive white, glistening dots within drusen seen by color photography. Macula-wide high-resolution histological sections through the fovea and superior perifovea of short post-mortem eyes were stained with toluidine blue. Sections were examined by light microscopy. Findings from each imaging modality were catalogued.

 
Results
 

Multimodal imaging was performed on 10 eyes. In AF imaging calcified drusen showed topographically influenced morphology. Calcified drusen in the center of macula typically showed loss of autofluorescence signal encompassed a broader area than the drusen themselves. More peripherally located neighboring calcified drusen showed autofluorescence loss in that was smaller proportionately. Peripheral to these calcified drusen were typical drusen with increased autofluorescence signal despite lacking demonstrable visible calcium, an appearance different from the autofluorescence pattern of conventional drusen. OCT demonstrated hyperreflective dots and curvilinear structures within calcified drusen, increased transmission of light surrounding the drusen in cases of geographic atrophy, and a larger overlying area of absent outer retinal bands. Of 19 calcified drusen in 6 donor eyes, all contained mineral deposits consistent with calcium. Overlying RPE was completely absent in 13, partially absent in 4, and intact in only 2. Some drusen contained Müller cell processes, RPE cells, or macrophages. Outer retinal atrophy, manifested by attenuated photoreceptor outer segments and blunted inner segments, was present overlying all calcified drusen independent of RPE status.

 
Conclusions
 

Calcification of drusen is considered to be a manifestation of drusen regression. There are widespread changes in the overlying retina and RPE that are larger, and can presage geographic atrophy. Calcified drusen are an important marker in the development of geographic atrophy. This study has demonstrated that multiple layers are concurrently involved, with potential impact on visual function and theories of disease pathogenesis.

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