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Anticholinergic Medication Burden and Cognitive Subtypes in Parkinson's Disease without Dementia.
- Source :
-
Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists [Arch Clin Neuropsychol] 2024 May 26. Date of Electronic Publication: 2024 May 26. - Publication Year :
- 2024
- Publisher :
- Ahead of Print
-
Abstract
- Objective: Cognitive changes are heterogeneous in Parkinson's disease (PD). This study compared whether anticholinergic burden drives differences in cognitive domain performance and empirically-derived PD-cognitive phenotypes.<br />Method: A retrospective chart review contained participants (n = 493) who had idiopathic PD without dementia. Participants' medications were scored (0-3) and summed based on the anticholinergic cognitive burden scale (ACBS). We examined the ACBS' relationship to five cognitive domain composites (normative z-scores) and three (K-means clustering based) cognitive phenotypes: cognitively intact, low executive function (EF), and predominately impaired EF/memory. Analyses included Spearman correlations, analysis of covariance, and Pearson chi-squared test.<br />Results: Overall, phenotypes did not differ in anticholinergic burden, and (after false-discovery-rate corrections) no cognitive domains related. When comparing those above and below the clinically relevant ACBS cutoff (i.e., score ≥3), no significant phenotype or domain differences were found.<br />Conclusions: Anticholinergic medication usage did not drive cognitive performance in a large clinical sample of idiopathic PD without dementia.<br /> (© The Author(s) 2024. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
Details
- Language :
- English
- ISSN :
- 1873-5843
- Database :
- MEDLINE
- Journal :
- Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists
- Publication Type :
- Academic Journal
- Accession number :
- 38797973
- Full Text :
- https://doi.org/10.1093/arclin/acae041