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Retinal Cell Damage in Diabetic Retinopathy

Diabetic retinopathy (DR), the most common microvascular complication that occurs in diabetes mellitus (DM), is the leading cause of vision loss in working-age adults. The prevalence of diabetic retinopathy is approximately 30% of the diabetic population and untreated DR can eventually cause blindne...

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Detalles Bibliográficos
Autores principales: Zhou, Jing, Chen, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177610/
https://www.ncbi.nlm.nih.gov/pubmed/37174742
http://dx.doi.org/10.3390/cells12091342
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author Zhou, Jing
Chen, Bo
author_facet Zhou, Jing
Chen, Bo
author_sort Zhou, Jing
collection PubMed
description Diabetic retinopathy (DR), the most common microvascular complication that occurs in diabetes mellitus (DM), is the leading cause of vision loss in working-age adults. The prevalence of diabetic retinopathy is approximately 30% of the diabetic population and untreated DR can eventually cause blindness. For decades, diabetic retinopathy was considered a microvascular complication and clinically staged by its vascular manifestations. In recent years, emerging evidence has shown that diabetic retinopathy causes early neuronal dysfunction and neurodegeneration that may precede vascular pathology and affect retinal neurons as well as glial cells. This knowledge leads to new therapeutic strategies aiming to prevent dysfunction of retinal neurons at the early stage of DR. Early detection and timely treatment to protect retinal neurons are critical to preventing visual loss in DR. This review provides an overview of DR and the structural and functional changes associated with DR, and discusses neuronal degeneration during diabetic retinopathy, the mechanisms underlying retinal neurodegeneration and microvascular complications, and perspectives on current and future clinic therapies.
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spelling pubmed-101776102023-05-13 Retinal Cell Damage in Diabetic Retinopathy Zhou, Jing Chen, Bo Cells Review Diabetic retinopathy (DR), the most common microvascular complication that occurs in diabetes mellitus (DM), is the leading cause of vision loss in working-age adults. The prevalence of diabetic retinopathy is approximately 30% of the diabetic population and untreated DR can eventually cause blindness. For decades, diabetic retinopathy was considered a microvascular complication and clinically staged by its vascular manifestations. In recent years, emerging evidence has shown that diabetic retinopathy causes early neuronal dysfunction and neurodegeneration that may precede vascular pathology and affect retinal neurons as well as glial cells. This knowledge leads to new therapeutic strategies aiming to prevent dysfunction of retinal neurons at the early stage of DR. Early detection and timely treatment to protect retinal neurons are critical to preventing visual loss in DR. This review provides an overview of DR and the structural and functional changes associated with DR, and discusses neuronal degeneration during diabetic retinopathy, the mechanisms underlying retinal neurodegeneration and microvascular complications, and perspectives on current and future clinic therapies. MDPI 2023-05-08 /pmc/articles/PMC10177610/ /pubmed/37174742 http://dx.doi.org/10.3390/cells12091342 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zhou, Jing
Chen, Bo
Retinal Cell Damage in Diabetic Retinopathy
title Retinal Cell Damage in Diabetic Retinopathy
title_full Retinal Cell Damage in Diabetic Retinopathy
title_fullStr Retinal Cell Damage in Diabetic Retinopathy
title_full_unstemmed Retinal Cell Damage in Diabetic Retinopathy
title_short Retinal Cell Damage in Diabetic Retinopathy
title_sort retinal cell damage in diabetic retinopathy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177610/
https://www.ncbi.nlm.nih.gov/pubmed/37174742
http://dx.doi.org/10.3390/cells12091342
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