The Curvature, Collagen Network Structure, and Their Relationship to the Pressure-Induced Strain Response of the Human Lamina Cribrosa in Normal and Glaucoma Eyes

Author:

Czerpak Cameron A.1,Ling Yik Tung Tracy1,Jefferys Joan L.2,Quigley Harry A.2,Nguyen Thao D.34ORCID

Affiliation:

1. Department of Mechanical Engineering, The Johns Hopkins University , Baltimore, MD 21218

2. Wilmer Ophthalmological Institute, School of Medicine, The Johns Hopkins University , Baltimore, MD 21287

3. Department of Mechanical Engineering, The Johns Hopkins University , Baltimore, MD 21218 ; , Baltimore, MD 21287

4. Wilmer Ophthalmological Institute, School of Medicine, The Johns Hopkins University , Baltimore, MD 21218 ; , Baltimore, MD 21287

Abstract

Abstract The lamina cribrosa (LC) is a connective tissue in the optic nerve head (ONH). The objective of this study was to measure the curvature and collagen microstructure of the human LC, compare the effects of glaucoma and glaucoma optic nerve damage, and investigate the relationship between the structure and pressure-induced strain response of the LC in glaucoma eyes. Previously, the posterior scleral cups of 10 normal eyes and 16 diagnosed glaucoma eyes were subjected to inflation testing with second harmonic generation (SHG) imaging of the LC and digital volume correlation (DVC) to calculate the strain field. In this study, we applied a custom microstructural analysis algorithm to the maximum intensity projection of SHG images to measure features of the LC beam and pore network. We also estimated the LC curvatures from the anterior surface of the DVC-correlated LC volume. Results showed that the LC in glaucoma eyes had larger curvatures p≤0.03), a smaller average pore area (p = 0.001), greater beam tortuosity (p < 0.0001), and more isotropic beam structure (p = 0.01) than in normal eyes. The difference measured between glaucoma and normal eyes may indicate remodeling of the LC with glaucoma or baseline differences that contribute to the development of glaucomatous axonal damage.

Funder

BrightFocus Foundation

Johns Hopkins University

National Eye Institute

National Science Foundation

U.S. Public Health Service

Publisher

ASME International

Subject

Physiology (medical),Biomedical Engineering

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