Tortuous Pore Path Through the Glaucomatous Lamina Cribrosa
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 path...
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| Published in | Scientific reports Vol. 8; no. 1; pp. 7281 - 7 |
|---|---|
| Main Authors | , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
London
Nature Publishing Group UK
08.05.2018
Nature Publishing Group Nature Portfolio |
| Subjects | |
| Online Access | Get full text |
| ISSN | 2045-2322 2045-2322 |
| DOI | 10.1038/s41598-018-25645-9 |
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| 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. |
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| AbstractList | 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.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. 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. 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. 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. |
| ArticleNumber | 7281 |
| Author | Lu, Chen Sigal, Ian A. Schuman, Joel S. Bilonick, Richard A. Liu, Jonathan Grulkowski, Ireneusz Lucy, Katie A. Ishikawa, Hiroshi Kagemann, Larry Wang, Bo Fujimoto, James G. Nadler, Zachary Wollstein, Gadi |
| Author_xml | – sequence: 1 givenname: Bo surname: Wang fullname: Wang, Bo organization: Department of Ophthalmology, University of Pittsburgh School of Medicine, UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh – sequence: 2 givenname: Katie A. surname: Lucy fullname: Lucy, Katie A. organization: NYU Eye Center, NYU Langone Health, Department of Ophthalmology, New York University School of Medicine – sequence: 3 givenname: Joel S. surname: Schuman fullname: Schuman, Joel S. email: joel.schuman@nyu.edu organization: NYU Eye Center, NYU Langone Health, Department of Ophthalmology, New York University School of Medicine, Department of Electrical and Computer Engineering, Tandon School of Engineering, New York University, Department of Neuroscience and Physiology, New York University School of Medicine – sequence: 4 givenname: Ian A. surname: Sigal fullname: Sigal, Ian A. organization: Department of Ophthalmology, University of Pittsburgh School of Medicine, UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh – sequence: 5 givenname: Richard A. surname: Bilonick fullname: Bilonick, Richard A. organization: Department of Ophthalmology, University of Pittsburgh School of Medicine, UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Biostatistics, University of Pittsburgh School of Public Health – sequence: 6 givenname: Chen surname: Lu fullname: Lu, Chen organization: Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology – sequence: 7 givenname: Jonathan surname: Liu fullname: Liu, Jonathan organization: Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology – sequence: 8 givenname: Ireneusz surname: Grulkowski fullname: Grulkowski, Ireneusz organization: Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology – sequence: 9 givenname: Zachary surname: Nadler fullname: Nadler, Zachary organization: Department of Ophthalmology, University of Pittsburgh School of Medicine, UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center – sequence: 10 givenname: Hiroshi orcidid: 0000-0001-6310-5748 surname: Ishikawa fullname: Ishikawa, Hiroshi organization: NYU Eye Center, NYU Langone Health, Department of Ophthalmology, New York University School of Medicine – sequence: 11 givenname: Larry surname: Kagemann fullname: Kagemann, Larry organization: NYU Eye Center, NYU Langone Health, Department of Ophthalmology, New York University School of Medicine, Center for Devices and Radiological Health, Food and Drug Administration – sequence: 12 givenname: James G. surname: Fujimoto fullname: Fujimoto, James G. organization: Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology – sequence: 13 givenname: Gadi orcidid: 0000-0001-7036-2726 surname: Wollstein fullname: Wollstein, Gadi organization: NYU Eye Center, NYU Langone Health, Department of Ophthalmology, New York University School of Medicine |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29740064$$D View this record in MEDLINE/PubMed |
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| Snippet | 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... Abstract The lamina cribrosa is a primary site of damage in glaucoma. While mechanical distortion is hypothesized to cause reduction of axoplasmic flow, little... |
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| SubjectTerms | 59 692/308/53 692/698/1688/512/2613 Aged Axonal Transport - physiology Axons Axons - pathology Eye Female Glaucoma Glaucoma, Open-Angle - physiopathology Humanities and Social Sciences Humans Image processing Intraocular Pressure - physiology Male Middle Aged multidisciplinary Nerve Fibers - pathology Nerve Fibers - physiology Ocular Hypertension - physiopathology Optic Disk - diagnostic imaging Optic Disk - physiopathology Optic nerve Optic Nerve - diagnostic imaging Optic Nerve - physiopathology Pores Retina Retinal Ganglion Cells - pathology Science Science (multidisciplinary) Segmentation Tomography, Optical Coherence |
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| Title | Tortuous Pore Path Through the Glaucomatous Lamina Cribrosa |
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