Role of inflammation in diabetic macular edema and neovascular age-related macular degeneration.

Diabetic macular edema Inflammation Intravitreal corticosteroid implant Neovascular age-related macular degeneration VEGF inhibitors

Journal

Survey of ophthalmology
ISSN: 1879-3304
Titre abrégé: Surv Ophthalmol
Pays: United States
ID NLM: 0404551

Informations de publication

Date de publication:
17 Jul 2024
Historique:
received: 07 12 2023
revised: 09 07 2024
accepted: 15 07 2024
medline: 20 7 2024
pubmed: 20 7 2024
entrez: 19 7 2024
Statut: aheadofprint

Résumé

Diabetic macular edema (DME) and neovascular age-related macular degeneration (nAMD) are multifactorial disorders that affect the macula and cause significant vision loss. Although inflammation and neoangiogenesis are hallmarks of DME and nAMD, respectively, they share some biochemical mediators. While inflammation is a trigger for the processes that lead to the development of DME, in nAMD inflammation seems to be the consequence of retinal pigment epithelium and Bruch membrane alterations. These pathophysiologic differences may be the key issue that justifies the difference in treatment strategies. Vascular endothelial growth factor inhibitors have changed the treatment of both diseases, however, many patients with DME fail to achieve the established therapeutic goals. From a clinical perspective, targeting inflammatory pathways with intravitreal corticosteroids has been proven to be effective in patients with DME. On the contrary, the clinical relevance of addressing inflammation in patients with nAMD has not been proven yet. We explore the role and implication of inflammation in the development of nAMD and DME and its therapeutical relevance.

Identifiants

pubmed: 39029747
pii: S0039-6257(24)00080-8
doi: 10.1016/j.survophthal.2024.07.006
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: S. Vujosevic is a consultant for Abbvie, Boehringer and Ingelheim, Bayer, Novartis, Roche, Zeiss. C. Astarita and V. Gallinari are AbbVie employee and may own AbbVie stocks/options. Disclosure of Conflicts of Interest This manuscript was funded by AbbVie S.r.l. AbbVie participated in writing, reviewing, and approving the publication. No honoraria or payments were made for authorship. Conflict-of-interest disclosure: S. Vujosevic is a consultant for Abbvie, Boehringer and Ingelheim, Bayer, Novartis, Roche, Zeiss. M. Lupidi, S. Donati and E. Pilotto have no conflicts of interest to declare. C. Astarita and V. Gallinari are AbbVie employee and may own AbbVie stocks/options.

Auteurs

Stela Vujosevic (S)

Department of Biomedical, Surgical and Dental Sciences University of Milan, Milan, Italy; Eye Clinic, IRCCS MultiMedica, Milan, Italy.

Marco Lupidi (M)

Eye Clinic, Department of Experimental and Clinical Medicine, Polytechnic University of Marche, Ancona, Italy. Electronic address: marcomed2@gmail.com.

Simone Donati (S)

Department of Medicine and Surgery, University of Insubria of Varese, Varese, Italy.

Carlo Astarita (C)

AbbVie S.r.l., SR 148 Pontina, 04011, Campoverde, LT, Italy.

Valentina Gallinaro (V)

AbbVie S.r.l., SR 148 Pontina, 04011, Campoverde, LT, Italy.

Elisabetta Pilotto (E)

Department of Neuroscience-Ophthalmology, University of Padova, Padova, Italy.

Classifications MeSH