Racial Differences in the Presentation and Progression of Huntington's Disease

Author:

Buchanan Danielle A.1ORCID,Brown Amy E.1ORCID,Osigwe Elicia C.2ORCID,Pfalzer Anna C.1ORCID,Mann Leah G.2ORCID,Yan Yan3ORCID,Kang Hakmook3ORCID,Claassen Daniel O.1ORCID

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.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference20 articles.

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