TY - JOUR
T1 - Developing SDOCT to assess donor human eyes prior to tissue sectioning for research
AU - Brown, Ninita H.
AU - Koreishi, Anjum F.
AU - McCall, Michelle
AU - Izatt, Joseph A.
AU - Rickman, Catherine Bowes
AU - Toth, Cynthia A.
N1 - Funding Information:
We gratefully acknowledge the financial support of the NIH under grant EB01630 (Brown), 5R21EY017393–02 (McCall, Izatt, Toth), and NEI P30EY005722 in addition to the Macular Vision Research Foundation (Bowes-Rickman), the Ruth and Milton Steinbach Fund (Bowes-Rickman), and the Research to Prevent Blindness William and Mary Greve Special Scholars Award (Bowes-Rickman).
Funding Information:
The authors have full control of all primary data, and agree to allow Graefe’s Archive for Clinical and Experimental Ophthalmology to review their data upon request. Financial disclosure McCall: Honoraria from Bioptigen Inc., Izatt: Equipment from Bioptigen, Inc., Consultant for Bioptigen, Inc., Licensed technology to Bioptigen, Inc. Toth: Research funding from: Genentech, Sirion Therapeutics, Bioptigen, Inc., Alcon Laboratories, Inc., NC Biotechnology Center; Consultant for Genentech, Licensed technology to Alcon Laboratories. N.H.Brown.J.A.Izatt.C.A.Toth Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA
PY - 2009
Y1 - 2009
N2 - Background: To compare spectral domain optical coherence tomography (SDOCT) cross-sectional images of human central retina obtained from donor eyes with and without age-related macular degeneration (AMD) to corresponding histopathology from light micrographs. To establish the utility of SDOCT for localizing pathology in the posterior eyecup, for identifying ocular disease in donor eyes, or for directing subsequent sectioning of retinal lesions for research. Methods: Seven consecutive human donor eyes were selected based on age. The eyes, with the anterior segment removed, were imaged by SDOCT with a focusing aspheric lens. Four eyes were from donors with a clinical history of AMD, and three were from age-matched donors with no history of AMD. Histopathological correlation of morphological changes detected in three eyes by SDOCT was obtained for comparison to step serial-sectioned light microscopy images of the formalin-fixed, paraffin-embedded retina. A simplified imaging setup was tested on an enucleated porcine eye for comparison. Results: AMD pathology was detected and localized in four eyes by SDOCT. The SDOCT images correlated with the histopathology observed by light microscopy in each sectioned eye. Pathologies included a subfoveal neovascular lesion with subretinal fluid, peripapillary neovascularization, epiretinal membrane, foveal cyst, choroidal folds, and drusen. Similar imaging was possible with the simplified setup. Conclusions: SDOCT imaging identified retinal disease of the posterior eyecup in human donor eyes. Pathology detected with SDOCT was verified by light microscopy in three eyes, supporting the utility of SDOCT as a screening tool for research.
AB - Background: To compare spectral domain optical coherence tomography (SDOCT) cross-sectional images of human central retina obtained from donor eyes with and without age-related macular degeneration (AMD) to corresponding histopathology from light micrographs. To establish the utility of SDOCT for localizing pathology in the posterior eyecup, for identifying ocular disease in donor eyes, or for directing subsequent sectioning of retinal lesions for research. Methods: Seven consecutive human donor eyes were selected based on age. The eyes, with the anterior segment removed, were imaged by SDOCT with a focusing aspheric lens. Four eyes were from donors with a clinical history of AMD, and three were from age-matched donors with no history of AMD. Histopathological correlation of morphological changes detected in three eyes by SDOCT was obtained for comparison to step serial-sectioned light microscopy images of the formalin-fixed, paraffin-embedded retina. A simplified imaging setup was tested on an enucleated porcine eye for comparison. Results: AMD pathology was detected and localized in four eyes by SDOCT. The SDOCT images correlated with the histopathology observed by light microscopy in each sectioned eye. Pathologies included a subfoveal neovascular lesion with subretinal fluid, peripapillary neovascularization, epiretinal membrane, foveal cyst, choroidal folds, and drusen. Similar imaging was possible with the simplified setup. Conclusions: SDOCT imaging identified retinal disease of the posterior eyecup in human donor eyes. Pathology detected with SDOCT was verified by light microscopy in three eyes, supporting the utility of SDOCT as a screening tool for research.
KW - Age-related macular degeneration
KW - Drusen
KW - Human donor eyes
KW - SDOCT
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U2 - 10.1007/s00417-009-1044-3
DO - 10.1007/s00417-009-1044-3
M3 - Article
C2 - 19225801
AN - SCOPUS:67651092393
SN - 0065-6100
VL - 247
SP - 1069
EP - 1080
JO - Albrecht von Graefes Archiv für Klinische und Experimentelle Ophthalmologie
JF - Albrecht von Graefes Archiv für Klinische und Experimentelle Ophthalmologie
IS - 8
ER -
