Longitudinal analysis of contrast acuity in Friedreich ataxia.

Neurol Genet

Department of Neurology (A.G.H., D.R.L.), University of Pennsylvania; Divisions of Neurology and Pediatrics (L.A.H., D.R.L.), Children's Hospital of Philadelphia, PA; Department of Neurology (S.P.), University of California at Los Angeles; Departments of Neurology and Pediatrics (K.M.), University of Iowa; Department of Neurology (G.R.W.), Emory University, Atlanta, GA; Department of Neurology (T.Z.), University of South Florida, Tampa Bay; Department of Neurology (S.H.S.), University of Florida, Gainesville; Department of Neurology (T.A.), Houston Methodist Hospital, TX; Murdoch Children's Research Institute (M.B.D.), Melbourne, Victoria, Australia; and Department of Neurology (A.B.), University of Rochester, NY.

Published: August 2018

AI Article Synopsis

  • The study aimed to investigate how visual acuity changes over time in patients with Friedreich ataxia, focusing on both high and low-contrast scenarios.
  • Over an average follow-up of 4.4 years involving 764 participants, results showed a significant decrease in visual acuity at various levels of contrast, with the decline being more pronounced at lower contrasts and in patients with higher GAA repeat lengths.
  • The findings suggest that low-contrast visual acuity could be an important indicator (biomarker) for tracking disease progression and response to treatments in Friedreich ataxia research.

Article Abstract

Objective: To determine the natural history of contrast acuity in Friedreich ataxia.

Methods: In the Friedreich Ataxia-Clinical Outcome Measures Study, participants (n = 764) underwent binocular high- and low-contrast visual acuity testing at annual study visits. Mixed-effects linear regression was used to model visual acuity as a function of time, with random intercepts and slopes to account for intraindividual correlation of repeated measurements. A time-varying covariate was used to adjust for diabetes, and interaction terms were used to assess for effect modification by GAA repeat length, disease duration, and other variables.

Results: Across a median of 4.4 years of follow-up, visual acuity decreased significantly at 100% contrast (-0.37 letters/y, 95% confidence interval [CI]: -0.52 to -0.21), 2.5% contrast (-0.81 letters/year, 95% CI: -0.99 to -0.65), and 1.25% contrast (-1.12 letters/y, 95% CI: -1.29 to -0.96 letters/year). There was a significant interaction between time and GAA repeat length such that the rate of decrease in visual acuity was greater for patients with higher GAA repeat lengths at 2.5% contrast ( = 0.018) and 1.25% contrast ( = 0.043) but not 100% contrast. There was no effect modification by age at onset after adjusting for GAA repeat length.

Conclusions: Low-contrast visual acuity decreases linearly over time in Friedreich ataxia, and the rate of decrease is greater at higher GAA repeat lengths. Contrast sensitivity has the potential to serve as a biomarker and surrogate outcome in future studies of Friedreich ataxia.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066362PMC
http://dx.doi.org/10.1212/NXG.0000000000000250DOI Listing

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