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Rho-Kinase Inhibitors for the Treatment of Refractory Diabetic Macular Oedema
Milagros Mateos-Olivares1, Luis García-Onrubia1,2, Fco Javier Valentín-Bravo1
1Department of Ophthalmology, Hospital Clínico Universitario de Valladolid, 47003 Valladolid, Spain.
Diabetic macular oedema (DMO) is a major cause of vision loss. Targeting Rho-kinase (ROCK) signaling may offer new treatments for DMO resistant to anti-VEGF therapies.
Area of Science:
- Ophthalmology
- Pharmacology
- Molecular Biology
Background:
- Diabetic macular oedema (DMO) is a leading cause of vision loss in diabetic retinopathy (DR).
- Intravitreal anti-VEGF injections are standard but not universally effective for DMO.
- Refractory DMO requires novel therapeutic strategies due to complex pathophysiology.
Purpose of the Study:
- To review the role of Rho-associated kinase (ROCK) in DMO pathogenesis.
- To explore the therapeutic potential of targeting the Rho/ROCK pathway for DMO treatment.
- To identify new drug targets for DMO refractory to current therapies.
Main Methods:
- Systematic literature search from 1991 to 2021.
- Keywords included: "rho-Associated Kinas-es", "Diabetic Retinopathy", "Macular Edema", "Ripasudil", "Fasudil", "Netarsudil".
Main Results:
- Rho-kinase (ROCK) is implicated in the pathogenesis of DMO.
- The Rho/ROCK signaling pathway presents a promising target for DMO therapeutics.
- Specific ROCK inhibitors like Ripasudil, Fasudil, and Netarsudil show potential.
Conclusions:
- Understanding ROCK's role is crucial for developing new DMO treatments.
- Targeting ROCK offers a potential strategy for managing anti-VEGF refractory DMO.
- Further research into ROCK inhibitors may lead to improved DMO prevention and treatment.
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