Evidence map›Paper›PMID 38551585›Full record

ArticleInvestigative ophthalmology & visual science2024

Forward Light Scattering of the Vitreous Gel After Enzymatic Aging: An In Vitro Model to Study Vitreous Opacification.

Maximilian Hammer, Marcel Muuss, Sonja Schickhardt, Alexander Scheuerle, Ramin Khoramnia, Grzegorz Labuz, Philipp Uhl, Gerd Uwe Auffarth

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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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

8 authors at 4 institutions in 1 country.

Maximilian HammerUniversity Eye Clinic Heidelberg, Heidelberg, Germany.
Marcel MuussUniversity Eye Clinic Heidelberg, Heidelberg, Germany.
Sonja SchickhardtThe David J Apple Laboratory for Vision Research, Heidelberg, Germany.
Alexander ScheuerleUniversity Eye Clinic Heidelberg, Heidelberg, Germany.
Ramin KhoramniaUniversity Eye Clinic Heidelberg, Heidelberg, Germany.
Grzegorz LabuzUniversity Eye Clinic Heidelberg, Heidelberg, Germany.
Philipp UhlInstitute for Pharmacy and Molecular Biotechnology, Heidelberg, Germany.
Gerd Uwe AuffarthUniversity Eye Clinic Heidelberg, Heidelberg, Germany.
University Hospital Heidelberg · DEApple (Germany) · DEAugenklinik Heidelberg · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Symptomatic vitreous opacifications, so-called floaters, are difficult to objectively assess majorly limiting the possibility of in vitro studies. Forward light scattering was found previously to be increased in eyes with symptomatic floaters. Using an objective setup to measure forward light scattering, we studied the effects of enzymatically digesting the components of the vitreous body on straylight to develop an in vitro model of vitreous opacifications. Methods: Fifty-seven porcine vitreous bodies were digested using hyaluronidase, collagenase, trypsin, and bromelain, as well as using a combination of hyaluronidase + collagenase and hyaluronidase + bromelain. A modified C-Quant setup was used to objectively assess forward light scattering. Results: Depletion of hyaluronic acid majorly increased vitreous straylight (mean increase 34.4 deg2/sr; P = 0.01), whereas primarily digesting the vitreous gel with collagenase or trypsin did not significantly affect straylight. When collagenase or bromelain is applied in hyaluronic acid depleted vitreous gels, the increase in forward light scattering is reversed partially. Conclusions: The age-related loss of hyaluronic acid primarily drives the increase in vitreous gel straylight induced by conglomerates of collagen. This process can be reversed partially by digesting collagen. This in vitro model allows the objective quantification and statistical comparison of straylight burden caused by vitreous opacities and, thus, can serve as a first testing ground for pharmacological therapies, as demonstrated with bromelain.

Indexed as

BromelainsLightAgingAnimalsCollagenCollagenasesHyaluronic AcidHyaluronoglucosaminidaseScattering, RadiationSwineTrypsinBromelainsCollagenCollagenasesHyaluronic AcidHyaluronoglucosaminidaseTrypsin

Identifiers

PMID38551585
PMCPMC10981431
OpenAlexW4393318690

What OpenQuestion holds

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LicenceCC BY
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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.