Impact of the Anticholinergic Burden on Disease-Specific Symptoms in Parkinsonian Syndromes

Author:

Mahmoudi Romina1,Greten Stephan1,Veith Sanches Linda1,Krey Lea1,Ulaganathan Sarana1,Höglinger Günter U.1234ORCID,Heck Johannes5ORCID,Wegner Florian1,Klietz Martin1ORCID

Affiliation:

1. Department of Neurology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany

2. Department of Neurology, University Hospital of Munich, Ludwig-Maximilians-Universität (LMU) Munich, 80539 Munich, Germany

3. Munich Cluster for Systems Neurology (SyNergy) Munich, 80539 Munich, Germany

4. German Center for Neurodegenerative Diseases (DZNE), 80539 Munich, Germany

5. Institute for Clinical Pharmacology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany

Abstract

Background: Anticholinergic adverse effects pose a relevant threat to patients, in particular elderly and cognitively impaired patients. Patients with Parkinsonian syndromes are especially at risk from anticholinergic adverse effects due to the often-required complex drug therapy. Aims: The aim of this study was to evaluate the potential effect of the anticholinergic burden on motor and non-motor symptoms in Parkinson’s disease and atypical Parkinsonian syndromes. Methods: This cross-sectional, monocentric retrospective data analysis included 151 patients with Parkinson’s disease (PD), 63 with progressive supranuclear palsy (PSP), and 36 with multiple system atrophy (MSA). The anticholinergic burden of patients’ medications was determined using two established scores: the Anticholinergic Drug Scale (ADS) and the German Anticholinergic Burden Scale (GABS). These scores were compared between the different diseases and correlated with several disease-specific scores. Results: Anticholinergic burden was higher in patients with PD, in particular, compared to PSP. In the PD group, anticholinergic burden showed a weak correlation with almost all analyzed clinical scores and the number of administered drugs. The UMSARS I and II showed a significant correlation with the anticholinergic burden in MSA patients. In general, the GABS-measured anticholinergic burden was significantly higher compared to the ADS-measured. Conclusions: The calculated anticholinergic burden affected motor and non-motor symptoms in patients with various Parkinsonian syndromes poorly. Since the GABS also contains basic anti-parkinsonian drugs, this score tended to overestimate the anticholinergic burden in patients with Parkinsonian syndromes and, therefore, seemed less appropriate for this application.

Funder

German Parkinson’s Disease Association

Publisher

MDPI AG

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