Evidence map›Paper›PMID 38566432›Full record

ArticleAging cell2024

Aging and intraocular pressure homeostasis in mice.

Guorong Li, Joseph van Batenburg-Sherwood, Babak N Safa, Nina Sara Fraticelli Guzmán, Andrea Wilson, Mohammad Reza Bahrani Fard, Kevin Choy, Michael L de Ieso, J Serena Cui, Andrew J Feola and 6 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
8.6field-weighted citation impact, top 2% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

16 citing papers in PubMed, 17 citations in OpenAlex.

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  12. TRPV4 and chloride channels mediate volume sensing in trabecular meshwork cells.American journal of physiology. Cell physiology · 2024
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  14. bioRxiv : the preprint server for biology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 2 countries.

Guorong LiDepartment of Ophthalmology, Duke University, Durham, North Carolina, USA.
Joseph van Batenburg-SherwoodDepartment of Bioengineering, Imperial College London, London, UK.
Babak N SafaWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia, USA.
Nina Sara Fraticelli GuzmánDepartment of Ophthalmology, Emory University, Atlanta, Georgia, USA.
Andrea WilsonDepartment of Ophthalmology, Duke University, Durham, North Carolina, USA.
Mohammad Reza Bahrani FardWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia, USA.
Kevin ChoyDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
Michael L de IesoDepartment of Ophthalmology, Duke University, Durham, North Carolina, USA.
J Serena CuiDepartment of Ophthalmology, Duke University, Durham, North Carolina, USA.
Andrew J FeolaDepartment of Ophthalmology, Emory University, Atlanta, Georgia, USA.
Tara WeiszDepartment of Ophthalmology, Duke University, Durham, North Carolina, USA.
Megan KuhnDepartment of Ophthalmology, Duke University, Durham, North Carolina, USA.
Catherine Bowes RickmanDepartment of Ophthalmology, Duke University, Durham, North Carolina, USA.
Sina FarsiuDepartment of Ophthalmology, Duke University, Durham, North Carolina, USA.
C Ross EthierWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia, USA.
W Daniel StamerDepartment of Ophthalmology, Duke University, Durham, North Carolina, USA.ORCID 0000-0002-2504-8997
Duke University · USGeorgia Institute of Technology · USEmory University · USImperial College London · GB

Funding

VISION RESEARCHP30EY005722 · NEI · DUKE UNIVERSITY · PI W Daniel Stamer · 1985 to 2026
$19.3M
P30-Core Grant for Vision Research Core CP30EY006360 · NEI · EMORY UNIVERSITY · PI BOATRIGHT, JEFFREY H · 1986 to 2025
$15.3M
VIsion Science Training in AtlantaT32EY007092 · NEI · EMORY UNIVERSITY · PI Machelle T. Pardue · 1985 to 2026
$4.6M
Quantitative assessment of glaucomatous conventional outflow dynamicsR01EY030124 · NEI · DUKE UNIVERSITY · PI C ROSS ETHIER, Sina Farsiu · 2019 to 2026
$4.0M
Complement factor H modulates lipoprotein clearance in AMDR01EY031748 · NEI · DUKE UNIVERSITY · PI BOWES RICKMAN, CATHERINE · 2020 to 2024
$2.8M
Molecular Mechanisms of Exfoliation GlaucomaR01EY030617 · NEI · DUKE UNIVERSITY · PI HAUSER, MICHAEL A, STAMER, W DANIEL · 2019 to 2023
$2.8M
Transcriptional and Biomechanical Analysis of Segmental Outflow in GlaucomaR01EY031710 · NEI · GEORGIA INSTITUTE OF TECHNOLOGY · PI ETHIER, C ROSS, GUPTA, DIVAKAR · 2020 to 2023
$2.4M
Impact of Menopause on the Aqueous Outflow PathwayR01EY030871 · NEI · GEORGIA INSTITUTE OF TECHNOLOGY · PI FEOLA, ANDREW J · 2020 to 2024
$1.6M
The role of iris biomechanics and sex differences in primary angle-closure glaucomaR00EY035360 · NEI · UNIVERSITY OF SOUTH FLORIDA · PI Babak Naghizadehsafa · 2024 to 2026
$747k
The role of iris biomechanics and sex differences in primary angle-closure glaucomaK99EY035360 · NEI · GEORGIA INSTITUTE OF TECHNOLOGY · PI NAGHIZADEH SAFA, BABAK · 2023 to 2024
$224k
The Effect of Estrogen Deficiencies on Vision Loss in GlaucomaIK2RX002342 · VA · VETERANS HEALTH ADMINISTRATION · PI FEOLA, ANDREW J · 2018 to 2023
–
Alfred P. Sloan Foundation G-2019-11435NEI NIH HHS EY005722NEI NIH HHS EY006360NEI NIH HHS EY007092NEI NIH HHS EY030124NEI NIH HHS EY030871NEI NIH HHS EY031710NEI NIH HHS EY031748NEI NIH HHS EY035360NEI NIH HHS K99 EY035360NEI NIH HHS P30 EY005722NEI NIH HHS P30 EY006360NEI NIH HHS R00 EY035360NEI NIH HHS R01 EY030124NEI NIH HHS R01 EY030617NEI NIH HHS R01 EY030871NEI NIH HHS R01 EY031710NEI NIH HHS R01 EY031748NEI NIH HHS T32 EY007092RRD VA IK2 RX002342The Brightfocus Foundation G2021005FThe Brightfocus Foundation Special Opportunity AwardU.S. Department of Veterans Affairs RX002342
6 · The paper itself

Abstract

Age and elevated intraocular pressure (IOP) are the two primary risk factors for glaucoma, an optic neuropathy that is the leading cause of irreversible blindness. In most people, IOP is tightly regulated over a lifetime by the conventional outflow tissues. However, the mechanistic contributions of age to conventional outflow dysregulation, elevated IOP and glaucoma are unknown. To address this gap in knowledge, we studied how age affects the morphology, biomechanical properties and function of conventional outflow tissues in C57BL/6 mice, which have an outflow system similar to humans. As reported in humans, we observed that IOP in mice was maintained within a tight range over their lifespan. Remarkably, despite a constellation of age-related changes to the conventional outflow tissues that would be expected to hinder aqueous drainage and impair homeostatic function (decreased cellularity, increased pigment accumulation, increased cellular senescence and increased stiffness), outflow facility, a measure of conventional outflow tissue fluid conductivity, was stable with age. We conclude that the murine conventional outflow system has significant functional reserve in healthy eyes. However, these age-related changes, when combined with other underlying factors, such as genetic susceptibility, are expected to increase risk for ocular hypertension and glaucoma.

Indexed as

AgingHomeostasisIntraocular PressureMice, Inbred C57BLAnimalsGlaucomaHumansMaleMiceaqueous humoroutflow facilitySchlemm's canaltrabecular meshwork

Identifiers

PMID38566432
PMCPMC11258442
OpenAlexW4393866106

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.