Evidence map›Paper›PMID 37108506›Full record

ArticleInternational journal of molecular sciences2023

Topical Application of Deglycating Enzymes as an Alternative Non-Invasive Treatment for Presbyopia.

Joris R Delanghe, Jeroen Beeckman, Koen Beerens, Jonas Himpe, Nezahat Bostan, Marijn M Speeckaert, Margo Notebaert, Manon Huizing, Elisabeth Van Aken

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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

9 authors at 3 institutions in 1 country.

Joris R DelangheDepartment of Diagnostic Sciences, Ghent University, 9000 Ghent, Belgium.ORCID 0000-0002-5702-6792
Jeroen BeeckmanDepartment of Electronics and Information Systems, Ghent University, 9000 Ghent, Belgium.ORCID 0000-0002-0711-2465
Koen BeerensDepartment of Biotechnology, Faculty of Bioscience Engineering, Ghent University, 9000 Ghent, Belgium.ORCID 0000-0001-6608-0443
Jonas HimpeDepartment of Diagnostic Sciences, Ghent University, 9000 Ghent, Belgium.
Nezahat BostanAntwerp Biobank, Antwerp University Hospital, 2650 Antwerp, Belgium.
Marijn M SpeeckaertDepartment of Internal Medicine, Ghent University, 9000 Ghent, Belgium.ORCID 0000-0001-9183-4390
Margo NotebaertDepartment of Diagnostic Sciences, Ghent University, 9000 Ghent, Belgium.
Manon HuizingAntwerp Biobank, Antwerp University Hospital, 2650 Antwerp, Belgium.ORCID 0000-0001-5331-9486
Elisabeth Van AkenDepartment of Head and Skin, Ghent University, 9000 Ghent, Belgium.ORCID 0000-0003-2418-701X
Ghent University · BEAntwerp University Hospital · BEResearch Foundation - Flanders · BE

Funding

IOF Ghent University -F2020/IOF-StarTT/034)
6 · The paper itself

Abstract

Presbyopia is an age-related vision disorder that is a global public health problem. Up to 85% of people aged ≥40 years develop presbyopia. In 2015, 1.8 billion people globally had presbyopia. Of those with significant near vision disabilities due to uncorrected presbyopia, 94% live in developing countries. Presbyopia is undercorrected in many countries, with reading glasses available for only 6-45% of patients living in developing countries. The high prevalence of uncorrected presbyopia in these parts of the world is due to the lack of adequate diagnosis and affordable treatment. The formation of advanced glycation end products (AGEs) is a non-enzymatic process known as the Maillard reaction. The accumulation of AGEs in the lens contributes to lens aging (leading to presbyopia and cataract formation). Non-enzymatic lens protein glycation induces the gradual accumulation of AGEs in aging lenses. AGE-reducing compounds may be effective at preventing and treating AGE-related processes. Fructosyl-amino acid oxidase (FAOD) is active on both fructosyl lysine and fructosyl valine. As the crosslinks encountered in presbyopia are mainly non-disulfide bridges, and based on the positive results of deglycating enzymes in cataracts (another disease caused by glycation of lens proteins), we studied the ex vivo effects of topical FAOD treatment on the power of human lenses as a new potential non-invasive treatment for presbyopia. This study demonstrated that topical FAOD treatment resulted in an increase in lens power, which is approximately equivalent to the correction obtained by most reading glasses. The best results were obtained for the newer lenses. Simultaneously, a decrease in lens opacity was observed, which improved lens quality. We also demonstrated that topical FAOD treatment results in a breakdown of AGEs, as evidenced by gel permeation chromatography and a marked reduction in autofluorescence. This study demonstrated the therapeutic potential of topical FAOD treatment in presbyopia.

Indexed as

CataractLens, CrystallinePresbyopiaAgingGlycation End Products, AdvancedHumansGlycation End Products, Advancedageingfructosyl-amino acid oxidaseglycationlenspresbyopia

Identifiers

PMID37108506
PMCPMC10139041
OpenAlexW4366090596

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.