Evidence map›Paper›PMID 38264539›Full record

ReviewDrug design, development and therapy2024

The Role of Rho Kinase Inhibitors in Corneal Diseases.

Stefan Futterknecht, Eleftherios Chatzimichail, Konstantin Gugleta, Georgios D Panos, Zisis Gatzioufas

Abstract readReview
In one paragraph

Review in Drug design, development and therapy, 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
–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

16 citing papers in PubMed.

  1. Trial
  2. BRD4 inhibition mitigates acute and chronic corneal injury following topical nitrogen mustard exposure.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  3. Article
  4. Netarsudil-associated conjunctival fragility.American journal of ophthalmology case reports · 2026
    Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Available Therapeutic Options for Corneal Neovascularization: A Review.International journal of molecular sciences · 2024
    Review
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

5 authors.

Stefan FutterknechtDepartment of Ophthalmology, University Hospital of Basel, Basel, Switzerland.ORCID 0009-0000-2594-4225
Eleftherios ChatzimichailDepartment of Ophthalmology, University Hospital of Basel, Basel, Switzerland.
Konstantin GugletaDepartment of Ophthalmology, University Hospital of Basel, Basel, Switzerland.
Georgios D Panos *Department of Ophthalmology, Queen's Medical Centre, Nottingham University Hospitals, Nottingham, UK.ORCID 0000-0001-8399-7456
Zisis Gatzioufas *Department of Ophthalmology, University Hospital of Basel, Basel, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cornea, as the outermost layer of the eye, plays a crucial role in vision by focusing light onto the retina. Various diseases and injuries can compromise its clarity, leading to impaired vision. This review aims to provide a thorough overview of the pharmacological properties, therapeutic potential and associated risks of Rho-associated protein kinase (ROCK) inhibitors in the management of corneal diseases. The article focuses on four key ROCK inhibitors: Y-27632, fasudil, ripasudil, and netarsudil, providing a comparative examination. Studies supporting the use of ROCK inhibitors highlight their efficacy across diverse corneal conditions. In Fuchs' endothelial corneal dystrophy, studies on the application of Y-27632, ripasudil, and netarsudil demonstrated noteworthy enhancements in corneal clarity, endothelial cell density, and visual acuity. In pseudophakic bullous keratopathy, the injection of Y-27632 together with cultured corneal endothelial cells into the anterior chamber lead to enhanced corneal endothelial cell density and improved visual acuity. Animal models simulating chemical injury to the cornea showed a reduction of neovascularization and epithelial defects after application of fasudil and in a case of iridocorneal endothelial syndrome netarsudil improved corneal edema. Addressing safety considerations, netarsudil and ripasudil, both clinically approved, exhibit adverse events such as conjunctival hyperemia, conjunctival hemorrhage, cornea verticillata, conjunctivitis, and blepharitis. Monitoring patients during treatment becomes crucial to balancing the potential therapeutic benefits with these associated risks. In conclusion, ROCK inhibitors, particularly netarsudil and ripasudil, offer promise in managing corneal diseases. The comparative analysis of their pharmacological properties and studies supporting their efficacy underscore their potential therapeutic significance. However, ongoing research is paramount to comprehensively understand their safety profiles and long-term outcomes in diverse corneal conditions, guiding their optimal application in clinical practice.

Indexed as

1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineAmidesBenzoatesbeta-AlanineCorneal DiseasesIsoquinolinesPyridinesrho-Associated KinasesSulfonamidesAnimalsEndothelial CellsHumans1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineAmidesBenzoatesbeta-AlaninefasudilIsoquinolinesK-115netarsudilPyridinesrho-Associated KinasesSulfonamidesY 27632corneacorneal diseasescorneal dystrophiescorneal transplantationFuchs’ endothelial corneal dystrophyrho kinase inhibitors

Identifiers

PMID38264539
PMCPMC10804875

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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.