New Therapies of Neovascular AMD—Beyond Anti-VEGFs

Neovascular age-related macular degeneration (nAMD) is one of the leading causes of blindness among the aging population. The current treatment options for nAMD include intravitreal injections of anti-vascular endothelial growth factor (anti-VEGF). However, standardized frequent administration of an...

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Main Author: Praveen Yerramothu
Format: Article
Language:English
Published: MDPI AG 2018-07-01
Series:Vision
Subjects:
Online Access:http://www.mdpi.com/2411-5150/2/3/31
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spelling doaj-f3c7b2a3ddfb401b83261d179cba50152020-11-25T01:43:58ZengMDPI AGVision2411-51502018-07-01233110.3390/vision2030031vision2030031New Therapies of Neovascular AMD—Beyond Anti-VEGFsPraveen Yerramothu0School of Optometry and Vision Science, University of New South Wales, Sydney 00098, AustraliaNeovascular age-related macular degeneration (nAMD) is one of the leading causes of blindness among the aging population. The current treatment options for nAMD include intravitreal injections of anti-vascular endothelial growth factor (anti-VEGF). However, standardized frequent administration of anti-VEGF injections only improves vision in approximately 30–40% of nAMD patients. Current therapies targeting nAMD pose a significant risk of retinal fibrosis and geographic atrophy (GA) development in nAMD patients. A need exists to develop new therapies to treat nAMD with effective and long-term anti-angiogenic effects. Recent research on nAMD has identified novel therapeutic targets and angiogenic signaling mechanisms involved in its pathogenesis. For example, tissue factor, human intravenous immune globulin, interferon-β signaling, cyclooxygenase-2 (COX-2) and cytochrome P450 monooxygenase lipid metabolites have been identified as key players in the development of angiogenesis in AMD disease models. Furthermore, novel therapies such as NACHT, LRR and PYD domains containing protein 3 (NLRP3) inflammasome inhibition, inhibitors of integrins and tissue factor are currently being tested at the level of clinical trials to treat nAMD. The aim of this review is to discuss the scope for alternative therapies proposed as anti-VEGFs for the treatment of nAMD.http://www.mdpi.com/2411-5150/2/3/31neovascular AMDnew therapiesanti-VEGFsAMD signaling
collection DOAJ
language English
format Article
sources DOAJ
author Praveen Yerramothu
spellingShingle Praveen Yerramothu
New Therapies of Neovascular AMD—Beyond Anti-VEGFs
Vision
neovascular AMD
new therapies
anti-VEGFs
AMD signaling
author_facet Praveen Yerramothu
author_sort Praveen Yerramothu
title New Therapies of Neovascular AMD—Beyond Anti-VEGFs
title_short New Therapies of Neovascular AMD—Beyond Anti-VEGFs
title_full New Therapies of Neovascular AMD—Beyond Anti-VEGFs
title_fullStr New Therapies of Neovascular AMD—Beyond Anti-VEGFs
title_full_unstemmed New Therapies of Neovascular AMD—Beyond Anti-VEGFs
title_sort new therapies of neovascular amd—beyond anti-vegfs
publisher MDPI AG
series Vision
issn 2411-5150
publishDate 2018-07-01
description Neovascular age-related macular degeneration (nAMD) is one of the leading causes of blindness among the aging population. The current treatment options for nAMD include intravitreal injections of anti-vascular endothelial growth factor (anti-VEGF). However, standardized frequent administration of anti-VEGF injections only improves vision in approximately 30–40% of nAMD patients. Current therapies targeting nAMD pose a significant risk of retinal fibrosis and geographic atrophy (GA) development in nAMD patients. A need exists to develop new therapies to treat nAMD with effective and long-term anti-angiogenic effects. Recent research on nAMD has identified novel therapeutic targets and angiogenic signaling mechanisms involved in its pathogenesis. For example, tissue factor, human intravenous immune globulin, interferon-β signaling, cyclooxygenase-2 (COX-2) and cytochrome P450 monooxygenase lipid metabolites have been identified as key players in the development of angiogenesis in AMD disease models. Furthermore, novel therapies such as NACHT, LRR and PYD domains containing protein 3 (NLRP3) inflammasome inhibition, inhibitors of integrins and tissue factor are currently being tested at the level of clinical trials to treat nAMD. The aim of this review is to discuss the scope for alternative therapies proposed as anti-VEGFs for the treatment of nAMD.
topic neovascular AMD
new therapies
anti-VEGFs
AMD signaling
url http://www.mdpi.com/2411-5150/2/3/31
work_keys_str_mv AT praveenyerramothu newtherapiesofneovascularamdbeyondantivegfs
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