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Carbonic anhydrase inhibitors in the management of macular edema: A review of the literature

BACKGROUND: Macular edema (ME) is a vision-threatening condition that commonly develops as a consequence of ocular diseases, including age-related macular degeneration, retinal vaso-occlusion of the central retinal vein and its branches, diabetic retinopathy, central serous chorioretinopathy, uveiti...

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Autor principal: Shahsuvaryan, Marianne L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Virtual Ophthalmic Research Center 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445326/
https://www.ncbi.nlm.nih.gov/pubmed/37641698
http://dx.doi.org/10.51329/mehdiophthal1443
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author Shahsuvaryan, Marianne L.
author_facet Shahsuvaryan, Marianne L.
author_sort Shahsuvaryan, Marianne L.
collection PubMed
description BACKGROUND: Macular edema (ME) is a vision-threatening condition that commonly develops as a consequence of ocular diseases, including age-related macular degeneration, retinal vaso-occlusion of the central retinal vein and its branches, diabetic retinopathy, central serous chorioretinopathy, uveitis, retinitis pigmentosa, pseudophakia, ocular trauma, and drug toxicity. The treatment of ME remains challenging, although steroids and vascular endothelial growth factor inhibitors are available. Cost-effective therapy using a noninvasive administration route is required. This study aimed at reviewing the role of carbonic anhydrase inhibitors (CAIs) in the management of ME. METHODS: A literature search was conducted using PubMed/MEDLINE and Google Scholar for studies from January 2000 to March 2022. The following keywords were used in various combinations: “macular edema”, “carbonic anhydrase”, “carbonic anhydrase inhibitors”, “acetazolamide”, “dorzolamide”, and “brinzolamide”. RESULTS: Articles with high or medium clinical relevance were selected for this review. We found that multiple studies have demonstrated the relevance and efficacy rates of CAIs in the management of ME. Most published studies focused on acetazolamide and dorzolamide, with nearly all studies reporting therapeutic responses. CONCLUSIONS: ME is the leading cause of vision loss and requires noninvasive and cost-effective pharmacotherapy. With progress in the understanding of ME, particularly the role of carbonic anhydrase as a key driver, CAIs are the focus of research. Further optimization of the choice of CAIs and retinal bioavailability, potentially with nanoparticle formulations, is required to enable the effective management of ME. Further research is warranted to address the therapeutic effects of CAIs in different formulations.
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spelling pubmed-104453262023-08-28 Carbonic anhydrase inhibitors in the management of macular edema: A review of the literature Shahsuvaryan, Marianne L. Med Hypothesis Discov Innov Ophthalmol Review Article BACKGROUND: Macular edema (ME) is a vision-threatening condition that commonly develops as a consequence of ocular diseases, including age-related macular degeneration, retinal vaso-occlusion of the central retinal vein and its branches, diabetic retinopathy, central serous chorioretinopathy, uveitis, retinitis pigmentosa, pseudophakia, ocular trauma, and drug toxicity. The treatment of ME remains challenging, although steroids and vascular endothelial growth factor inhibitors are available. Cost-effective therapy using a noninvasive administration route is required. This study aimed at reviewing the role of carbonic anhydrase inhibitors (CAIs) in the management of ME. METHODS: A literature search was conducted using PubMed/MEDLINE and Google Scholar for studies from January 2000 to March 2022. The following keywords were used in various combinations: “macular edema”, “carbonic anhydrase”, “carbonic anhydrase inhibitors”, “acetazolamide”, “dorzolamide”, and “brinzolamide”. RESULTS: Articles with high or medium clinical relevance were selected for this review. We found that multiple studies have demonstrated the relevance and efficacy rates of CAIs in the management of ME. Most published studies focused on acetazolamide and dorzolamide, with nearly all studies reporting therapeutic responses. CONCLUSIONS: ME is the leading cause of vision loss and requires noninvasive and cost-effective pharmacotherapy. With progress in the understanding of ME, particularly the role of carbonic anhydrase as a key driver, CAIs are the focus of research. Further optimization of the choice of CAIs and retinal bioavailability, potentially with nanoparticle formulations, is required to enable the effective management of ME. Further research is warranted to address the therapeutic effects of CAIs in different formulations. International Virtual Ophthalmic Research Center 2022-04-01 /pmc/articles/PMC10445326/ /pubmed/37641698 http://dx.doi.org/10.51329/mehdiophthal1443 Text en © Author(s). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Review Article
Shahsuvaryan, Marianne L.
Carbonic anhydrase inhibitors in the management of macular edema: A review of the literature
title Carbonic anhydrase inhibitors in the management of macular edema: A review of the literature
title_full Carbonic anhydrase inhibitors in the management of macular edema: A review of the literature
title_fullStr Carbonic anhydrase inhibitors in the management of macular edema: A review of the literature
title_full_unstemmed Carbonic anhydrase inhibitors in the management of macular edema: A review of the literature
title_short Carbonic anhydrase inhibitors in the management of macular edema: A review of the literature
title_sort carbonic anhydrase inhibitors in the management of macular edema: a review of the literature
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445326/
https://www.ncbi.nlm.nih.gov/pubmed/37641698
http://dx.doi.org/10.51329/mehdiophthal1443
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