Evidence map›Paper›PMID 40081750›Full record

ArticleExperimental eye research2025

Biomechanical contributions to murine lens shape: Confinement, compaction, and residual stresses.

Matthew A Reilly

Abstract read
In one paragraph

Article in Experimental eye research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Matthew A ReillyDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH, USA; Department of Ophthalmology & Visual Sciences, The Ohio State University, Columbus, OH, USA. Electronic address: reilly.196@osu.edu.

Funding

The Ohio State University Vision Sciences Research Core Program (OSU-VSRCP)P30EY032857 · NEI · OHIO STATE UNIVERSITY · PI Nathan Doble · 2022 to 2026
$3.6M
Biomechanics of Lens MorphogenesisR01EY035278 · NEI · OHIO STATE UNIVERSITY · PI Matthew A Reilly · 2023 to 2026
$1.5M
NEI NIH HHS P30 EY032857NEI NIH HHS R01 EY035278
6 · The paper itself

Abstract

Presbyopia is the progressive loss of near vision with age and affects nearly everyone by age 50. This most common visual deficit is a result of age-related changes in lens shape and refractive index, which dictate the optical power of the fully accommodated lens. Lens shape in the absence of external loads is dictated by the balance of biomechanical forces between the lens and its capsule. These residual stresses arise from differential growth. However, these stresses remain unknown. This study uses the nearly spherical murine lens as a model for elucidating how these residual stresses may be calculated and which experimental parameters must be measured to enable such calculations. Several key concepts arise from the analysis in agreement with recent studies. It is suggested that the lens fiber cells are poroelastic and that fiber cell compaction arises from biomechanical confinement effects of the lens capsule. It is possible to computationally "recapsulate" the uncompacted lens after growth, then estimate the extent to which the capsule compacts the fiber cells and, in turn, the extent to which the fiber cells distend the capsule. The simple biomechanical models presented are capable of predicting residual stresses in line with published experimental measurements, suggesting that they capture the essence of how the lens and capsule push and pull during years of differential growth.

Indexed as

Lens, CrystallineModels, BiologicalPresbyopiaAgingAnimalsBiomechanical PhenomenaElasticityLens Capsule, CrystallineMiceMice, Inbred C57BLStress, Mechanical

Identifiers

PMID40081750
PMCPMC12333461

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.