Abstract

The lamina cribrosa is a primary site of damage in glaucoma. While mechanical distortion is hypothesized to cause reduction of axoplasmic flow, little is known about how the pores, which contains the retinal ganglion cell axons, traverse the lamina cribrosa. We investigated lamina cribrosa pore paths in vivo to quantify differences in tortuosity of pore paths between healthy and glaucomatous eyes. We imaged 16 healthy, 23 glaucoma suspect and 48 glaucomatous eyes from 70 subjects using a swept source optical coherence tomography system. The lamina cribrosa pores were automatically segmented using a previously described segmentation algorithm. Individual pore paths were automatically tracked through the depth of the lamina cribrosa using custom software. Pore path convergence to the optic nerve center and tortuosity was quantified for each eye. We found that lamina cribrosa pore pathways traverse the lamina cribrosa closer to the optic nerve center along the depth of the lamina cribrosa regardless of disease severity or diagnostic category. In addition, pores of glaucoma eyes take a more tortuous path through the lamina cribrosa compared to those of healthy eyes, suggesting a potential mechanism for reduction of axoplasmic flow in glaucoma.

Details

Title
Tortuous Pore Path Through the Glaucomatous Lamina Cribrosa
Author
Wang, Bo 1 ; Lucy, Katie A 2 ; Schuman, Joel S 3 ; Sigal, Ian A 1 ; Bilonick, Richard A 4 ; Chen, Lu 5 ; Liu, Jonathan 5 ; Grulkowski, Ireneusz 5 ; Nadler, Zachary 6 ; Ishikawa, Hiroshi 2   VIAFID ORCID Logo  ; Kagemann, Larry 7 ; Fujimoto, James G 5 ; Wollstein, Gadi 2   VIAFID ORCID Logo 

 Department of Ophthalmology, University of Pittsburgh School of Medicine, UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Pittsburgh, PA, United States; Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh, PA, United States 
 NYU Eye Center, NYU Langone Health, Department of Ophthalmology, New York University School of Medicine, New York, NY, United States 
 NYU Eye Center, NYU Langone Health, Department of Ophthalmology, New York University School of Medicine, New York, NY, United States; Department of Electrical and Computer Engineering, Tandon School of Engineering, New York University, New York, NY, United States; Department of Neuroscience and Physiology, New York University School of Medicine, New York, NY, United States 
 Department of Ophthalmology, University of Pittsburgh School of Medicine, UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Pittsburgh, PA, United States; Department of Biostatistics, University of Pittsburgh School of Public Health, Pittsburgh, PA, United States 
 Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA, United States 
 Department of Ophthalmology, University of Pittsburgh School of Medicine, UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Pittsburgh, PA, United States 
 NYU Eye Center, NYU Langone Health, Department of Ophthalmology, New York University School of Medicine, New York, NY, United States; Center for Devices and Radiological Health, Food and Drug Administration, Silver Spring, MD, United States 
Pages
1-7
Publication year
2018
Publication date
May 2018
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2036470957
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.