Reticular pseudodrusen: A critical phenotype in age-related macular degeneration.

Prog Retin Eye Res

Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Australia; Ophthalmology, Department of Surgery, The University of Melbourne, Melbourne, Australia. Electronic address:

Published: May 2022

AI Article Synopsis

  • Reticular pseudodrusen (RPD) are lesions associated with age-related macular degeneration (AMD) that have gained recognition due to advancements in imaging technology, highlighting their significance in the disease.
  • Despite their importance, challenges in defining RPD and accounting for other AMD factors hinder a full understanding of their independent effects on vision loss.
  • This review aims to clarify the prevalence and clinical relevance of RPD, proposing a new imaging definition and exploring potential mechanisms behind their formation and impact on AMD progression.

Article Abstract

Reticular pseudodrusen (RPD), or subretinal drusenoid deposits (SDD), refer to distinct lesions that occur in the subretinal space. Over the past three decades, their presence in association with age-related macular degeneration (AMD) has become increasingly recognized, especially as RPD have become more easily distinguished with newer clinical imaging modalities. There is also an increasing appreciation that RPD appear to be a critical AMD phenotype, where understanding their pathogenesis will provide further insights into the processes driving vision loss in AMD. However, key barriers to understanding the current evidence related to the independent impact of RPD include the heterogeneity in defining their presence, and failure to account for the confounding impact of the concurrent presence and severity of AMD pathology. This review thus critically discusses the current evidence on the prevalence and clinical significance of RPD and proposes a clinical imaging definition of RPD that will help move the field forward in gathering further key knowledge about this critical phenotype. It also proposes a putative mechanism for RPD formation and how they may drive progression to vision loss in AMD, through examining current evidence and presenting novel findings from preclinical and clinical studies.

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http://dx.doi.org/10.1016/j.preteyeres.2021.101017DOI Listing

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