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Anticholinergic Medication Burden and Cognitive Subtypes in Parkinson's Disease without Dementia.

Authors :
Santos LG
Kenney LE
Ray A
Paredes A
Ratajska AM
Eversole K
Patel B
Rawls AE
Okun MS
Bowers D
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