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Longitudinal analysis of contrast acuity in Friedreich ataxia

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...

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Autores principales: Hamedani, Ali G., Hauser, Lauren A., Perlman, Susan, Mathews, Katherine, Wilmot, George R., Zesiewicz, Theresa, Subramony, S.H., Ashizawa, Tetsuo, Delatycki, Martin B., Brocht, Alicia, Lynch, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066362/
https://www.ncbi.nlm.nih.gov/pubmed/30065952
http://dx.doi.org/10.1212/NXG.0000000000000250
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author Hamedani, Ali G.
Hauser, Lauren A.
Perlman, Susan
Mathews, Katherine
Wilmot, George R.
Zesiewicz, Theresa
Subramony, S.H.
Ashizawa, Tetsuo
Delatycki, Martin B.
Brocht, Alicia
Lynch, David R.
author_facet Hamedani, Ali G.
Hauser, Lauren A.
Perlman, Susan
Mathews, Katherine
Wilmot, George R.
Zesiewicz, Theresa
Subramony, S.H.
Ashizawa, Tetsuo
Delatycki, Martin B.
Brocht, Alicia
Lynch, David R.
author_sort Hamedani, Ali G.
collection PubMed
description 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 (p = 0.018) and 1.25% contrast (p = 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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spelling pubmed-60663622018-07-31 Longitudinal analysis of contrast acuity in Friedreich ataxia Hamedani, Ali G. Hauser, Lauren A. Perlman, Susan Mathews, Katherine Wilmot, George R. Zesiewicz, Theresa Subramony, S.H. Ashizawa, Tetsuo Delatycki, Martin B. Brocht, Alicia Lynch, David R. Neurol Genet Article 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 (p = 0.018) and 1.25% contrast (p = 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. Wolters Kluwer 2018-07-23 /pmc/articles/PMC6066362/ /pubmed/30065952 http://dx.doi.org/10.1212/NXG.0000000000000250 Text en Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Hamedani, Ali G.
Hauser, Lauren A.
Perlman, Susan
Mathews, Katherine
Wilmot, George R.
Zesiewicz, Theresa
Subramony, S.H.
Ashizawa, Tetsuo
Delatycki, Martin B.
Brocht, Alicia
Lynch, David R.
Longitudinal analysis of contrast acuity in Friedreich ataxia
title Longitudinal analysis of contrast acuity in Friedreich ataxia
title_full Longitudinal analysis of contrast acuity in Friedreich ataxia
title_fullStr Longitudinal analysis of contrast acuity in Friedreich ataxia
title_full_unstemmed Longitudinal analysis of contrast acuity in Friedreich ataxia
title_short Longitudinal analysis of contrast acuity in Friedreich ataxia
title_sort longitudinal analysis of contrast acuity in friedreich ataxia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066362/
https://www.ncbi.nlm.nih.gov/pubmed/30065952
http://dx.doi.org/10.1212/NXG.0000000000000250
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