Longitudinal associations of anticholinergic medications on cognition and possible mitigating role of physical activity.


Journal

Journal of the American Geriatrics Society
ISSN: 1532-5415
Titre abrégé: J Am Geriatr Soc
Pays: United States
ID NLM: 7503062

Informations de publication

Date de publication:
06 2023
Historique:
revised: 24 12 2022
received: 03 08 2022
accepted: 15 01 2023
pmc-release: 01 06 2024
medline: 12 6 2023
pubmed: 15 2 2023
entrez: 14 2 2023
Statut: ppublish

Résumé

Many older adults take at least one prescription medication with anticholinergic (ACH) activity, which can impact the central nervous system and can lead to cognitive decline and impairment especially in an aging population susceptible to cognitive changes. We examined this relationship between ACH burden and cognitive function in middle-aged and older adults. We further determined if increased activity levels mitigated the relationships between ACH burden and cognition. Data from The Reasons for Geographic and Racial Differences in Stroke project were used. We included 20,575 adults aged ≥45 years with longitudinal cognitive testing. The anticholinergic cognitive burden (ACB) scale was used to assess for ACH use and overall burden. Cognitive data included an overall composite score, a memory, and verbal fluency composites. Mixed effects models were conducted to determine if cognitive function worsened over time for participants with higher ACB (>3) scores. The full model adjusted for age, sex, race, education, diabetes, hypertension, cardiovascular disease, congestive heart failure, and dyslipidemia, self-reported physical activity (PA) and depressive symptoms. A significant relationship between ACH burden and composite cognitive scores was found (p = <0.001), with those with higher ACB showing more rapid cognitive decline over time. There was an effect of age for participants with higher ACB (>3) scores and ACB as a continuous variable. Baseline PA level was associated with less cognitive decline over time and this effect was greater in older cohorts. We observed an effect of ACHs on cognition in adults ≥45 years old that worsened with age. ACH users showed more cognitive effects, whereas PA emerged as a possible mitigating factor.

Sections du résumé

BACKGROUND
Many older adults take at least one prescription medication with anticholinergic (ACH) activity, which can impact the central nervous system and can lead to cognitive decline and impairment especially in an aging population susceptible to cognitive changes. We examined this relationship between ACH burden and cognitive function in middle-aged and older adults. We further determined if increased activity levels mitigated the relationships between ACH burden and cognition.
METHODS
Data from The Reasons for Geographic and Racial Differences in Stroke project were used. We included 20,575 adults aged ≥45 years with longitudinal cognitive testing. The anticholinergic cognitive burden (ACB) scale was used to assess for ACH use and overall burden. Cognitive data included an overall composite score, a memory, and verbal fluency composites. Mixed effects models were conducted to determine if cognitive function worsened over time for participants with higher ACB (>3) scores. The full model adjusted for age, sex, race, education, diabetes, hypertension, cardiovascular disease, congestive heart failure, and dyslipidemia, self-reported physical activity (PA) and depressive symptoms.
RESULTS
A significant relationship between ACH burden and composite cognitive scores was found (p = <0.001), with those with higher ACB showing more rapid cognitive decline over time. There was an effect of age for participants with higher ACB (>3) scores and ACB as a continuous variable. Baseline PA level was associated with less cognitive decline over time and this effect was greater in older cohorts.
CONCLUSIONS
We observed an effect of ACHs on cognition in adults ≥45 years old that worsened with age. ACH users showed more cognitive effects, whereas PA emerged as a possible mitigating factor.

Identifiants

pubmed: 36786273
doi: 10.1111/jgs.18279
pmc: PMC10258136
mid: NIHMS1871303
doi:

Substances chimiques

Cholinergic Antagonists 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1937-1943

Subventions

Organisme : NINDS NIH HHS
ID : U01 NS041588
Pays : United States

Informations de copyright

© 2023 The Authors. Journal of the American Geriatrics Society published by Wiley Periodicals LLC on behalf of The American Geriatrics Society.

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Auteurs

Amani M Norling (AM)

Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Evelyn F. McKnight Brain Institute, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Aleena Bennett (A)

Department of Biostatistics, School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Michael Crowe (M)

Department of Psychology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

D Leann Long (DL)

Department of Biostatistics, School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Sara A Nolin (SA)

Department of Psychology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Terina Myers (T)

Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Evelyn F. McKnight Brain Institute, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Victor A Del Bene (VA)

Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Evelyn F. McKnight Brain Institute, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Ronald M Lazar (RM)

Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Evelyn F. McKnight Brain Institute, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Adam Gerstenecker (A)

Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Evelyn F. McKnight Brain Institute, University of Alabama at Birmingham, Birmingham, Alabama, USA.

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