Evidence map›Paper›PMID 40565122›Full record

ReviewInternational journal of molecular sciences2025

Pharmacological Strategies for Cataract Management: From Molecular Targets to Clinical Translation.

Laura de Diego-García, Raquel Rejas-González, Ignacio Cereza Latre, Ana Guzman-Aranguez

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. 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

4 authors.

Laura de Diego-GarcíaDepartment of Biochemistry and Molecular Biology, Facultad de Óptica y Optometría, Universidad Complutense de Madrid, 28037 Madrid, Spain.ORCID 0000-0002-1404-5803
Raquel Rejas-GonzálezChronic Disease Programme, UFIEC, Instituto de Salud Carlos III, 28220 Majadahonda, Spain.ORCID 0000-0002-4614-2536
Ignacio Cereza LatreDepartment of Biochemistry and Molecular Biology, Facultad de Óptica y Optometría, Universidad Complutense de Madrid, 28037 Madrid, Spain.
Ana Guzman-AranguezDepartment of Biochemistry and Molecular Biology, Facultad de Óptica y Optometría, Universidad Complutense de Madrid, 28037 Madrid, Spain.ORCID 0000-0001-6722-2044

Funding

Instituto de Salud Carlos III PI23/00607
6 · The paper itself

Abstract

Cataracts, characterized by the opacification of the eye lens, remain a leading cause of reversible blindness globally. Age and diabetes are key risk factors, and with the increasing aging and diabetic population, the global burden of cataracts is projected to rise significantly. Current treatment is predominantly surgical; however, pharmacological strategies could offer a non-invasive alternative with the potential to delay, prevent, or even reverse cataract progression. Recent research has enhanced our understanding of cataractogenesis, emphasizing oxidative stress as a key underlying mechanism, but also including other processes such as calcium dysregulation and altered lens homeostasis or specific events induced by hyperglycemia in diabetic cataracts. New therapeutic approaches have emerged considering the molecular mechanisms involved in cataracts, most of which focus on pharmacological agents with antioxidant properties. Additionally, small-molecule chaperones, aldose reductase inhibitors, and protein aggregation inhibitors have also demonstrated potential in stabilizing or restoring lens protein structure and transparency. While experimental results have shown encouraging results, further research is needed to optimize drug delivery systems to the lens, assess long-term safety, and confirm the clinical efficacy of these treatments. This article reviews current progress in pharmacological treatments for cataracts, outlining challenges and prospects for future integration into clinical practice.

Indexed as

CataractAnimalsAntioxidantsHumansLens, CrystallineMolecular Targeted TherapyOxidative StressAntioxidantsaldose reductase inhibitorsantioxidantcataractdrug deliveryoxidative stresspharmacologyprotein aggregation inhibitors

Identifiers

PMID40565122
PMCPMC12193184

What OpenQuestion holds

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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 OpenQuestion graph.