Affiliation:
1. Division of Cognitive and Behavioral Neurology, Department of Neurology Vanderbilt University Medical Center Nashville Tennessee USA
2. Department of Neuroscience Vanderbilt University Nashville Tennessee USA
3. Department of Biostatistics, Vanderbilt University Nashville Tennessee USA
Abstract
AbstractBackgroundHuntington's disease (HD) is an autosomal dominant neurodegenerative disease that predominantly impacts a Caucasian population, but few efforts have explored racial differences in presentation and progression.ObjectiveThe aim was to assess the presentation and progression of HD across race groups using the Enroll‐HD longitudinal observational study.MethodsWe applied propensity score matching for cytosine–adenine–guanine age product score, and age, to identify White, Hispanic, Asian, and Black participants from the Enroll‐HD database. We compared clinical presentations at baseline, and progression over time, using White participants as a control cohort.ResultsBlack participants were more severe at baseline across all clinical measures. No significant differences in progression were observed between race groups.ConclusionsWe consider the factors driving clinical differences at baseline for Black participants. Our data emphasize the necessary improvement in underrepresented minority recruitment for studies of rare diseases. © 2023 International Parkinson and Movement Disorder Society.
Subject
Neurology (clinical),Neurology
Cited by
3 articles.
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