| Literature DB >> 33847998 |
Ru-Ik Chee1, Abdallah Mahrous1, Lisa Koenig1, Lindsay Skye Mandel1, Fahd Yazdanie1, Chi-Chao Chan2, Mrinali P Gupta3,4.
Abstract
Aging is associated with a number of histological changes in the choroid, Bruch's membrane, RPE, and neuroretina. Outside of the normal physiologic aging spectrum of changes, abnormal deposits such as basal laminar deposits, basal linear deposits, and soft drusen are known to be associated with AMD. Progression of AMD to advanced stages involving geographic atrophy, choroidal neovascularization, and/or disciform scars can result in debilitating vision loss. Knowledge of the angiogenic pathway and its components that stimulate neovascularization has led to the development of a new paradigm of intravitreal anti-VEGF pharmacotherapy in the management of neovascular AMD. Currently however, there are no available treatments for the modification of disease progression in non-neovascular AMD, or for the treatment of geographic atrophy. Further understanding of the histopathology of AMD and the molecular mechanisms that contribute to pathogenesis of the disease may reveal additional therapeutic targets.Entities:
Keywords: Age-related macular degeneration; Basal laminar deposits; Basal linear deposits; Choroidal neovascularization; Disciform scar; Drusen; Geographic atrophy; Histopathology
Year: 2021 PMID: 33847998 DOI: 10.1007/978-3-030-66014-7_3
Source DB: PubMed Journal: Adv Exp Med Biol ISSN: 0065-2598 Impact factor: 2.622