June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
A novel micro-computed tomography (μCT) method to measure IOP-induced deformation of the Lamina Cribrosa (LC)
Author Affiliations & Notes
  • Baptiste Coudrillier
    Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA
  • Diogo M Geraldes
    Biomechanics, Imperial College, London, United Kingdom
  • Nghia Vo
    Diamond Light Source, Didcot, United Kingdom
  • Julie Albon
    School of Optometry and Vision Sciences, Cardiff University, Cardiff, United Kingdom
  • Richard L Abel
    Surgery, Imperial College, London, United Kingdom
  • Ian Campbell
    Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA
  • C Ross Ethier
    Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA
  • Footnotes
    Commercial Relationships Baptiste Coudrillier, None; Diogo Geraldes, None; Nghia Vo, None; Julie Albon, None; Richard Abel, None; Ian Campbell, None; C Ethier, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 6149. doi:
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      Baptiste Coudrillier, Diogo M Geraldes, Nghia Vo, Julie Albon, Richard L Abel, Ian Campbell, C Ross Ethier; A novel micro-computed tomography (μCT) method to measure IOP-induced deformation of the Lamina Cribrosa (LC) . Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):6149.

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

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Abstract
 
Purpose
 

To determine high-resolution, acute, IOP-induced deformation of LC beams, relevant to the mechanobiology of glaucoma.

 
Methods
 

Two porcine eyes and 7 human donor eyes were received within 24 hours of death and stored at -4C. Unfixed posterior poles were inflated to 6, 15, 22, and 30 mmHg using custom built pressurization chambers. High-resolution phase-contrast μCT scans were performed at the beamline I12-JEEP, Diamond Light Source (53 keV, 3600 projections, 0.08s exposure time, 2.56 μm isotropic resolution). LC beams were segmented in 3D, following Frangi’s filter image processing to determine beam position and LC microarchitecture. Histograms of pore size, pore density, and LC beam thickness were generated using Matlab and compared between IOP levels. The central cross-sections of the LC were manually delineated to determine the pressure-induced change in LC shape. Full-field 3D measurement of strains within the LC was achieved using digital volume correlation (DVC, LaVision).

 
Results
 

LC beams in high-resolution 3D scans of the entire unfixed LC were successfully segmented (Fig 1). The porcine LC mechanical response to IOP was nonlinear with largest deformation occurring between 6 and 15 mmHg. Elevated IOP was associated with a decrease in pore size, thinning of the LC beams and sclera, and posterior displacement of the LC. DVC measured strains with an accuracy of 0.1%. Mean first principal strain in the pig LC due to IOP increasing from 6 to 15 mmHg was 3.3% (range: 1.2-6.9%, Fig 2).

 
Conclusions
 

Phase-contrast μCT is a powerful tool to measure 3D changes in shape and microarchitecture of the human and porcine LC induced by increased IOP. Segmentation methods and algorithms to compute IOP-induced deformations from the 3D scans were validated on the porcine LC and are currently being applied to human LCs.  

 
Transverse sections of a phase-contrast μCT scan of an untreated human LC (top row) and pig LC (bottom row) at 6 mmHg.
 
Transverse sections of a phase-contrast μCT scan of an untreated human LC (top row) and pig LC (bottom row) at 6 mmHg.
 
 
Deformation of the pig LC. A: 3D reconstruction of a porcine LC after Frangi filtering and segmentation of LC beams (top) and average LC porosity vs IOP (bottom). B: Manual delineation of the LC and sclera at different pressures in longitudinal optical sections. IOP increase was associated with LC and scleral thinning and posterior displacement. C: First principal LC strain map at 15 mmHg calculated using DVC (top) and average strain vs IOP (bottom).
 
Deformation of the pig LC. A: 3D reconstruction of a porcine LC after Frangi filtering and segmentation of LC beams (top) and average LC porosity vs IOP (bottom). B: Manual delineation of the LC and sclera at different pressures in longitudinal optical sections. IOP increase was associated with LC and scleral thinning and posterior displacement. C: First principal LC strain map at 15 mmHg calculated using DVC (top) and average strain vs IOP (bottom).

 
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