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Grants > Using Genetics and Retinal Imaging to Predict Progression to Advanced AMD Updated On: Jan. 21, 2025
Macular Degeneration Research Grant

Using Genetics and Retinal Imaging to Predict Progression to Advanced AMD

Genes & Macular Degeneration
William Scott, PhD

Principal Investigator

William Scott, PhD

University of Miami Miller School of Medicine

Miami, FL, USA

About the Research Project

Program

Macular Degeneration Research

Award Type

Standard

Award Amount

$160,000

Active Dates

July 01, 2018 - December 30, 2020

Grant ID

M2018112

Acknowledgement

This grant is made possible by support from Dr. H. James and Carole Free.

Goals

Age-related macular degeneration (AMD) is the leading cause of irreversible blindness in older adults in the United States. The factors that determine progression from early AMD (with little vision loss) to advanced AMD (with more severe vision loss) are poorly understood. We will use detailed clinical examinations of the eye and large-scale genetic analysis to identify new genetic factors that are associated with changes in the eye over time and with development of advanced AMD. The results of this study will improve our understanding of the AMD disease process and provide potential avenues for development of targeted therapies.

Summary

The goal of our project is to identify genetic factors that influence progression of age-related macular degeneration (AMD) from early stages (where vision loss is less severe) to late stages (where there is significant visual impairment). Our study builds on an existing group of 400 individuals with early AMD who have been followed for at least two years and have had genetic factors measured across the genome. The first aim of our project is to analyze ocular coherence tomography (OCT) images taken at our first study visit (the “baseline exam”) where early AMD was detected. These images will be evaluated for several features that might predict progression to more severe disease, and these features will be examined for association with genetic factors. In the second specific aim, we will examine these baseline OCT features for association with the time that it takes to progress to late AMD. We will also determine if the influence of these OCT features on progression is modified by genetic factors. Identifying measurable factors that predict progression to late AMD might help us design tailored clinical follow-up strategies (more frequent visits for those most at risk of progression, for example). Identifying genetic factors that predict faster or slower progression could also provide targets for the development of potential therapies.