Dementia Associated with Anticholinergic Drugs Used for Overactive Bladder: A Nested Case-Control Study Using the French National Medical-Administrative Database.


Journal

The Journal of urology
ISSN: 1527-3792
Titre abrégé: J Urol
Pays: United States
ID NLM: 0376374

Informations de publication

Date de publication:
10 2022
Historique:
pubmed: 11 6 2022
medline: 14 9 2022
entrez: 10 6 2022
Statut: ppublish

Résumé

We analyzed the relationship between use of anticholinergic drugs to treat overactive bladder (OAB) and risk of incident dementia in older patients, overall and for each drug separately. We conducted a nested case-control study using the French National Medical-Administrative Database. We identified incident dementia cases and controls from January 1, 2013 to December 31, 2018 in individuals aged ≥60 years. Controls were matched 5:1 to cases by date of case diagnosis (index date), age, sex, and income. We set a 5-year exposure period ending 2 years before the index date (lag-time period to avoid protopathic bias). We quantified cumulative exposure to flavoxate, oxybutynin, solifenacin, trospium, and fesoterodine using defined daily doses (DDDs). We performed conditional logistic regression analyses adjusted for factors known to be associated with OAB and/or dementia including obesity, diabetes, stroke, coronary heart disease, and psychotic disorders. We analyzed 4,810 cases and 24,050 matched controls with a median age of 82 years. OAB anticholinergic use was associated with an increased risk of dementia (adjusted OR [aOR]=1.23, 95% CI 1.10-1.37) with a cumulative dose-response: aOR=1.07 (95% CI 0.91-1.25) for 1-90 DDDs, aOR=1.29 (1.05-1.58) for 91-365 DDDs and aOR=1.48 (1.22-1.80) for >365 DDDs. Considering each OAB anticholinergic separately showed a particularly marked increased risk of dementia for oxybutynin and solifenacin, but no increased risk for trospium. When treating OAB in older patients, OAB anticholinergics should be used with caution, taking into account the patient's cognitive status, the anticholinergic load, and the different therapeutic options.

Identifiants

pubmed: 35686842
doi: 10.1097/JU.0000000000002804
doi:

Substances chimiques

Cholinergic Antagonists 0
Muscarinic Antagonists 0
Solifenacin Succinate KKA5DLD701

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

863-871

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Marie France Malcher (MF)

Department of Biostatistics, Clinical Epidemiology, Public Health, and Innovation in Methodology, CHU Nîmes, University Montpellier, Nîmes, France.

Stephane Droupy (S)

Department of Urology and Andrology, CHU Nîmes, University of Montpellier, Nîmes, France.

Claudine Berr (C)

University of Montpellier, INSERM, INM (Institute for Neurosciences of Montpellier), Montpellier, France.

Abdelkrim Ziad (A)

ClinSearch-110, Malakoff, France.

Helena Huguet (H)

Clinical Research and Epidemiology Unit, CHU de Montpellier, University of Montpellier, Montpellier, France.

Jean-Luc Faillie (JL)

Department of Medical Pharmacology and Toxicology, CHU Montpellier University Hospital, Montpellier, France.
Institute Desbrest of Epidemiology and Public Health, UMR UA11 INSERM, University of Montpellier, Montpellier, France.

Chris Serrand (C)

Department of Biostatistics, Clinical Epidemiology, Public Health, and Innovation in Methodology, CHU Nîmes, University Montpellier, Nîmes, France.

Thibault Mura (T)

Department of Biostatistics, Clinical Epidemiology, Public Health, and Innovation in Methodology, CHU Nîmes, University Montpellier, Nîmes, France.
University of Montpellier, INSERM, INM (Institute for Neurosciences of Montpellier), Montpellier, France.

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Classifications MeSH