Cholinesterase inhibitors are associated with reduced mortality in patients with Alzheimer's disease and previous myocardial infarction.

Cholinesterase inhibitors Coronary artery disease Dementia Mortality Myocardial infarction

Journal

European heart journal. Cardiovascular pharmacotherapy
ISSN: 2055-6845
Titre abrégé: Eur Heart J Cardiovasc Pharmacother
Pays: England
ID NLM: 101669491

Informations de publication

Date de publication:
15 Jan 2024
Historique:
received: 08 09 2023
revised: 13 11 2023
accepted: 18 12 2023
medline: 15 1 2024
pubmed: 15 1 2024
entrez: 15 1 2024
Statut: aheadofprint

Résumé

Cholinesterase inhibitors (ChEIs) are the first-line symptomatic pharmacologic treatment for patients with mild-to-moderate Alzheimer's disease (AD). Although the target organ for this group of drugs is the brain, inhibition of the enzyme may affect cardiac function through vagotonic and anti-inflammatory effects. To assess the impact of ChEIs on outcomes in patients with AD who have experienced myocardial infarction (MI) prior to the AD diagnosis. Patients who had experienced MI before they were diagnosed with AD or Alzheimer's mixed dementia between 2008 and 2018 were identified from the Swedish Dementia Registry (SveDem, www.svedem.se), which was linked to the National Patient Registry to obtain data on MI and mortality. Cox proportional hazards regression model among a propensity score-matched dataset was performed to assess the association between ChEI treatment and clinical outcomes. Of 3198 patients with previous MI and a diagnosis of AD or mixed dementia, 1705 (53%) were on treatment with ChEIs. Patients treated with ChEIs were more likely to be younger and have a better overall cardiovascular (CV) risk profile. The incidence rate of all-cause death (per 1000 patient-years) in the propensity-matched cohort of 1016 ChEI users and 1016 non-users was 168.6 in patients on treatment with ChEIs compared with 190.7 in patients not on treatment with ChEIs. In this propensity-matched cohort, treatment with ChEIs was associated with a significantly lower risk of all-cause death (adjusted hazard ratio 0.81, 95% confidence interval 0.71-0.92) and a greater reduction with higher doses of ChEIs. While in the unadjusted analysis, ChEIs were associated with a lower risk of both CV and non-CV death, only the association with non-CV death remained significant after accounting for baseline differences. Treatment with ChEIs was associated with a significantly reduced risk of all-cause death, driven by lower rates of non-CV death in a nationwide cohort of patients with previous MI and a diagnosis of AD or mixed dementia. These associations were greater with higher ChEI doses. We assessed the association between cholinesterase inhibitors (ChEIs) and clinical outcomes in a nationwide cohort of patients with previous myocardial infarction (MI) and a diagnosis of Alzheimer's disease (AD) or mixed dementi. In propensity-matched analysis, treatment with ChEIs was associated with a 19% reduction in all-cause death driven by non-cardiovascular death. The reduction in all-cause death was greater with the higher doses of ChEIs.

Sections du résumé

BACKGROUND BACKGROUND
Cholinesterase inhibitors (ChEIs) are the first-line symptomatic pharmacologic treatment for patients with mild-to-moderate Alzheimer's disease (AD). Although the target organ for this group of drugs is the brain, inhibition of the enzyme may affect cardiac function through vagotonic and anti-inflammatory effects.
OBJECTIVE OBJECTIVE
To assess the impact of ChEIs on outcomes in patients with AD who have experienced myocardial infarction (MI) prior to the AD diagnosis.
METHODS METHODS
Patients who had experienced MI before they were diagnosed with AD or Alzheimer's mixed dementia between 2008 and 2018 were identified from the Swedish Dementia Registry (SveDem, www.svedem.se), which was linked to the National Patient Registry to obtain data on MI and mortality. Cox proportional hazards regression model among a propensity score-matched dataset was performed to assess the association between ChEI treatment and clinical outcomes.
RESULTS RESULTS
Of 3198 patients with previous MI and a diagnosis of AD or mixed dementia, 1705 (53%) were on treatment with ChEIs. Patients treated with ChEIs were more likely to be younger and have a better overall cardiovascular (CV) risk profile. The incidence rate of all-cause death (per 1000 patient-years) in the propensity-matched cohort of 1016 ChEI users and 1016 non-users was 168.6 in patients on treatment with ChEIs compared with 190.7 in patients not on treatment with ChEIs. In this propensity-matched cohort, treatment with ChEIs was associated with a significantly lower risk of all-cause death (adjusted hazard ratio 0.81, 95% confidence interval 0.71-0.92) and a greater reduction with higher doses of ChEIs. While in the unadjusted analysis, ChEIs were associated with a lower risk of both CV and non-CV death, only the association with non-CV death remained significant after accounting for baseline differences.
CONCLUSION CONCLUSIONS
Treatment with ChEIs was associated with a significantly reduced risk of all-cause death, driven by lower rates of non-CV death in a nationwide cohort of patients with previous MI and a diagnosis of AD or mixed dementia. These associations were greater with higher ChEI doses.
CONDENSED ABSTRACT CONCLUSIONS
We assessed the association between cholinesterase inhibitors (ChEIs) and clinical outcomes in a nationwide cohort of patients with previous myocardial infarction (MI) and a diagnosis of Alzheimer's disease (AD) or mixed dementi. In propensity-matched analysis, treatment with ChEIs was associated with a 19% reduction in all-cause death driven by non-cardiovascular death. The reduction in all-cause death was greater with the higher doses of ChEIs.

Identifiants

pubmed: 38224338
pii: 7542308
doi: 10.1093/ehjcvp/pvad102
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Swedish Research Council
ID : #2020-02014
Organisme : Swedish Association of Local Authorities and Regions
ID : #FoUI-975207
Organisme : VINNOVA
ID : #2021-02680
Organisme : KI Foundations
Organisme : Brain Foundation
ID : #FO2021-0331
Organisme : Erling-Persson Foundation
Organisme : Center for Innovative Medicine Foundation
ID : #FoUI-963369
Organisme : Åke Wibergs Foundation
ID : #M22-0170
Organisme : Swedish Society of Medicine
ID : #2022-01631
Organisme : Foundation for Geriatric Diseases at Karolinska Institutet
ID : 2022-01278
Organisme : Region Stockholm Clinical Appointment
ID : 988371
Organisme : Swedish Heart-Lung Foundation
ID : 20220524
Organisme : European Union
ID : 101053962
Organisme : Swedish State Support for Clinical Research
ID : #ALFGBG-71320
Organisme : Alzheimer Drug Discovery Foundation
ID : #201809-2016862
Organisme : AD Strategic Fund and the Alzheimer's Association
ID : #ADSF-21-831376-C
Organisme : Olav Thon Foundation
Organisme : Erling-Persson Family Foundation
Organisme : Stiftelsen för Gamla Tjänarinnor
Organisme : Hjärnfonden
ID : #FO2022-0270
Organisme : EU Joint Programme - Neurodegenerative Disease Research
ID : JPND2021-00694
Organisme : National Institute for Health and Care Research
Organisme : University College London Hospitals Biomedical Research Centre
Organisme : UK Dementia Research Institute
ID : UKDRI-1003

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

Bahira Shahim (B)

Heart, Vascular and Neuro Theme, Karolinska University Hospital, 17177 Stockholm, Sweden.
Department of Medicine Solna, Karolinska Institutet, 17177 Stockholm, Sweden.

Hong Xu (H)

Department of Neurobiology, Care Sciences and Society, Division of Clinical Geriatrics, Karolinska Institutet, 17177 Stockholm, Sweden.

Kristina Haugaa (K)

Heart, Vascular and Neuro Theme, Karolinska University Hospital, 17177 Stockholm, Sweden.
Department of Medicine Solna, Karolinska Institutet, 17177 Stockholm, Sweden.

Henrik Zetterberg (H)

Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at the University of Gothenburg, 41345 Mölndal, Sweden.
Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, 41345 Mölndal, Sweden.
UK Dementia Research Institute at UCL, London, UK.
Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.
Hong Kong Center for Neurodegenerative Diseases, Hong Kong SAR, China.
Wisconsin Alzheimer's Disease Research Center, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA.

Juliane Jurga (J)

Heart, Vascular and Neuro Theme, Karolinska University Hospital, 17177 Stockholm, Sweden.
Department of Medicine Solna, Karolinska Institutet, 17177 Stockholm, Sweden.

Dorota Religa (D)

Department of Neurobiology, Care Sciences and Society, Division of Clinical Geriatrics, Karolinska Institutet, 17177 Stockholm, Sweden.
Theme Inflammation and Aging, Karolinska University Hospital, Huddinge, Sweden.

Maria Eriksdotter (M)

Department of Neurobiology, Care Sciences and Society, Division of Clinical Geriatrics, Karolinska Institutet, 17177 Stockholm, Sweden.
Theme Inflammation and Aging, Karolinska University Hospital, Huddinge, Sweden.

Classifications MeSH