Evidence map›Paper›PMID 35660940›Full record

ArticleComputer methods and programs in biomedicine2022

Modeling the biomechanics of the conventional aqueous outflow pathway microstructure in the human eye.

Alireza Karimi, Reza Razaghi, Seyed Mohammadali Rahmati, J Crawford Downs, Ted S Acott, Ruikang K Wang, Murray Johnstone

Abstract read
In one paragraph

Article in Computer methods and programs in biomedicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

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0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Article
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  6. Minimally Invasive Glaucoma Surgery Procedure in the Human Eye. A Fluid Structure Interaction Study.International journal for numerical methods in biomedical engineering · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Alireza KarimiDepartment of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, 1670 University Boulevard, VH 372B, Birmingham, AL 35294, USA. Electronic address: akarimi@uabmc.edu.
Reza RazaghiDepartment of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, 1670 University Boulevard, VH 372B, Birmingham, AL 35294, USA.
Seyed Mohammadali RahmatiSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
J Crawford DownsDepartment of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, 1670 University Boulevard, VH 372B, Birmingham, AL 35294, USA.
Ted S AcottOphthalmology and Biochemistry and Molecular Biology, Casey Eye Institute, Oregon Health & Science University, Portland, OR, USA.
Ruikang K WangDepartment of Ophthalmology, University of Washington, Seattle, WA, USA; Department of Bioengineering, University of Washington, Seattle, WA, USA.
Murray JohnstoneDepartment of Ophthalmology, University of Washington, Seattle, WA, USA.

Funding

Proteomics CoreP30EY010572 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI John Peter Campbell · 1995 to 2026
$19.4M
Visual Phenotyping CoreP30EY003039 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Paul Douglas Gamlin · 1985 to 2026
$16.9M
Molecular Mechanisms of Outflow Segmentation and Intraocular Pressure HomeostasisR01EY025721 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI ACOTT, TED S · 2015 to 2022
$2.8M
The Aqueous Humor Outflow ResistanceR01EY030238 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TED S ACOTT · 2019 to 2026
$2.7M
Age-related changes in optic nerve head structure and biomechanicsR01EY018926 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DOWNS, J CRAWFORD, GIRKIN, CHRISTOPHER ANTHONY · 2008 to 2015
$2.6M
Ultra-wide field optical coherence tomography based angiography for imaging diabetic retinopathyR01EY028753 · NEI · UNIVERSITY OF WASHINGTON · PI WANG, RUIKANG · 2018 to 2021
$2.2M
Optic Nerve Head Mechanobiology in GlaucomaR01EY027924 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DOWNS, J CRAWFORD, MURPHY-ULLRICH, JOANNE E · 2018 to 2021
$1.8M
NON-INVASIVE REAL-TIME LABEL-FREE 3D IMAGING OF RETINAL MICROCIRCULATIONR01EY024158 · NEI · UNIVERSITY OF WASHINGTON · PI WANG, RUIKANG · 2014 to 2017
$1.7M
Modulation of Outflow Facility and BiomechanicsR01EY036011 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Alireza Karimi · 2024 to 2026
$1.2M
NEI NIH HHS P30 EY003039NEI NIH HHS P30 EY010572NEI NIH HHS R01 EY018926NEI NIH HHS R01 EY024158NEI NIH HHS R01 EY025721NEI NIH HHS R01 EY027924NEI NIH HHS R01 EY028753NEI NIH HHS R01 EY030238NEI NIH HHS R01 EY036011
6 · The paper itself

Abstract

BACKGROUND AND

objectiveIntraocular pressure (IOP) is determined by aqueous humor outflow resistance, which is a function of the combined resistance of Schlemm's canal (SC) endothelium and the trabecular meshwork (TM) and their interactions in the juxtacanalicular connective tissue (JCT) region. Aqueous outflow in the conventional outflow pathway results in pressure gradient across the TM, JCT, and SC inner wall, and induces mechanical stresses and strains that influence the geometry and homeostasis of the outflow system. The outflow resistance is affected by alteration in tissues' geometry, so there is potential for active, two-way, fluid-structure interaction (FSI) coupling between the aqueous humor (fluid) and the TM, JCT, and SC inner wall (structure). However, our understanding of the biomechanical interactions of the aqueous humor with the outflow connective tissues and its contribution to the outflow resistance regulation is incomplete.

methodsIn this study, a microstructural finite element (FE) model of a human eye TM, JCT, and SC inner wall was constructed from a segmented, high-resolution histologic 3D reconstruction of the human outflow system. Three different elastic moduli (0.004, 0.128, and 51.5 MPa based on prior reports) were assigned to the TM/JCT complex while the elastic modulus of the SC inner wall was kept constant at 0.00748 MPa. The hydraulic conductivity was programmed separately for the TM, JCT, and SC inner wall using a custom subroutine. Cable elements were embedded into the TM and JCT extracellular matrix to represent the directional stiffness imparted by anisotropic collagen fibril orientation. The resultant stresses and strains in the outflow system were calculated using fluid-structure interaction method.

resultsThe higher TM/JCT stiffness resulted in larger stresses, but smaller strains in the outflow connective tissues, and resulted in a 4- and 5-fold larger pressure drop across the SC inner wall, respectively, compared to the most compliant model. Funneling through µm-sized SC endothelial pores was evident in the models at lower tissue stiffness, but aqueous flow was more turbulent in models with higher TM/JCT stiffness.

conclusionsThe mechanical properties of the outflow tissues play a crucial role in the hydrodynamics of the aqueous humor in the conventional outflow system.

Indexed as

Aqueous HumorTrabecular MeshworkBiomechanical PhenomenaHumansHydrodynamicsIntraocular PressureComputational fluid dynamicsFluid-structure interactionJuxtacanalicular tissueOutflow resistanceSchlemm's canalTrabecular meshwork

Identifiers

PMID35660940
PMCPMC10424784

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