Evidence map›Paper›PMID 34359853›Full record

ReviewCells2021

Rho-Kinase Inhibitors for the Treatment of Refractory Diabetic Macular Oedema.

Milagros Mateos-Olivares, Luis García-Onrubia, Fco Javier Valentín-Bravo, Rogelio González-Sarmiento, Maribel Lopez-Galvez, J Carlos Pastor, Ricardo Usategui-Martín, Salvador Pastor-Idoate

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. A human-specificMolecular therapy. Nucleic acids · 2025
    Article
  3. Review
  4. Article
  5. Article
  6. The Application of Rho Kinase Inhibitors in the Management of Glaucoma.International journal of molecular sciences · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. 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

8 authors at 4 institutions in 2 countries.

Milagros Mateos-OlivaresDepartment of Ophthalmology, Hospital Clínico Universitario de Valladolid, 47003 Valladolid, Spain.
Luis García-OnrubiaDepartment of Ophthalmology, Hospital Clínico Universitario de Valladolid, 47003 Valladolid, Spain.
Fco Javier Valentín-BravoDepartment of Ophthalmology, Hospital Clínico Universitario de Valladolid, 47003 Valladolid, Spain.
Rogelio González-SarmientoArea of Infectious, Inflammatory and Metabolic Disease, Institute of Biomedical Research of Salamanca (IBSAL), 37007 Salamanca, Spain.ORCID 0000-0002-2726-6795
Maribel Lopez-GalvezDepartment of Ophthalmology, Hospital Clínico Universitario de Valladolid, 47003 Valladolid, Spain.
J Carlos PastorDepartment of Ophthalmology, Hospital Clínico Universitario de Valladolid, 47003 Valladolid, Spain.ORCID 0000-0001-5934-7306
Ricardo Usategui-MartínRetina Group, IOBA (Institute of Applied Ophthalmobiology), University of Valladolid, 47002 Valladolid, Spain.
Salvador Pastor-IdoateDepartment of Ophthalmology, Hospital Clínico Universitario de Valladolid, 47003 Valladolid, Spain.
Universidad de Valladolid · ESHospital Clínico Universitario de Valladolid · ESSt Thomas' Hospital · GBUniversidad de Salamanca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic macular oedema (DMO) is one of the leading causes of vision loss associated with diabetic retinopathy (DR). New insights in managing this condition have changed the paradigm in its treatment, with intravitreal injections of antivascular endothelial growth factor (anti-VEGF) having become the standard therapy for DMO worldwide. However, there is no single standard therapy for all patients DMO refractory to anti-VEGF treatment; thus, further investigation is still needed. The key obstacles in developing suitable therapeutics for refractory DMO lie in its complex pathophysiology; therefore, there is an opportunity for further improvements in the progress and applications of new drugs. Previous studies have indicated that Rho-associated kinase (Rho-kinase/ROCK) is an essential molecule in the pathogenesis of DMO. This is why the Rho/ROCK signalling pathway has been proposed as a possible target for new treatments. The present review focuses on the recent progress on the possible role of ROCK and its therapeutic potential in DMO. A systematic literature search was performed, covering the years 1991 to 2021, using the following keywords: "rho-Associated Kinas-es", "Diabetic Retinopathy", "Macular Edema", "Ripasudil", "Fasudil" and "Netarsudil". Better insight into the pathological role of Rho-kinase/ROCK may lead to the development of new strategies for refractory DMO treatment and prevention.

Indexed as

AnimalsDiabetic RetinopathyHumansMacular EdemaProtein Kinase InhibitorsRetinarho-Associated KinasesSignal TransductionTranslational Research, BiomedicalProtein Kinase Inhibitorsrho-Associated Kinasesdiabetic macular oedemadiabetic retinopathymacular oedemarho-associated kinases

Identifiers

PMID34359853
PMCPMC8307715
OpenAlexW3180941103

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.