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Benzodiazepine and Z-Drug Use and the Risk of Developing Dementia

BACKGROUND: Benzodiazepines (BZDs) and Z-drugs (BZDRs) are among the most prescribed medications for anxiety and insomnia, especially among older adults. Our objective was to investigate the association between the use of BZDRs and the risk of dementia. METHODS: A community-based retrospective cohor...

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Autores principales: Torres-Bondia, Francisco, Dakterzada, Farida, Galván, Leonardo, Buti, Miquel, Besanson, Gaston, Grill, Eric, Buil, Roman, de Batlle, Jordi, Piñol-Ripoll, Gerard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017765/
https://www.ncbi.nlm.nih.gov/pubmed/34727174
http://dx.doi.org/10.1093/ijnp/pyab073
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author Torres-Bondia, Francisco
Dakterzada, Farida
Galván, Leonardo
Buti, Miquel
Besanson, Gaston
Grill, Eric
Buil, Roman
de Batlle, Jordi
Piñol-Ripoll, Gerard
author_facet Torres-Bondia, Francisco
Dakterzada, Farida
Galván, Leonardo
Buti, Miquel
Besanson, Gaston
Grill, Eric
Buil, Roman
de Batlle, Jordi
Piñol-Ripoll, Gerard
author_sort Torres-Bondia, Francisco
collection PubMed
description BACKGROUND: Benzodiazepines (BZDs) and Z-drugs (BZDRs) are among the most prescribed medications for anxiety and insomnia, especially among older adults. Our objective was to investigate the association between the use of BZDRs and the risk of dementia. METHODS: A community-based retrospective cohort study was conducted based on the data available from 2002 to 2015 in Catalan Health Service. This cohort included all BZDR users (N = 83 138) and nonusers (N = 84 652) older than 45 years. A minimum 5-year lag window and an adjustment for psychiatric problems were applied for the data analysis. RESULTS: The hazard ratio (HR) for the risk of incident dementia among BZDR users was 1.22 (95% CI = 1.15 to 1.31). This risk was not significant after adjusting the data confounding factors (HR = 1.01; 95% CI = 0.94 to 1.08). We observed a higher risk with short-to-intermediate half-life BZDs (HR = 1.11; 95% CI = 1.04 to 1.20) and Z-drugs (HR = 1.20; 95% CI = 1.07 to 1.33) than for intermediate-to-long half-life BZDs (HR = 1.01; 95% CI = 0.94 to 1.08). We demonstrated a higher risk of incident dementia (HR = 1.23; 95% CI = 1.07 to 1.41 and odds ratio = 1.38; 95% CI = 1.27 to 1.50, respectively) in patients who received 91 to 180 defined daily doses (DDDs) and >180 DDDs compared with patients who received <90 DDD. Regarding patient sex, the risk of dementia was higher in women than in men. CONCLUSION: We found that the incidence of dementia was not higher among all BZDR users. Short half-life BZDs and Z-drugs increased the risk of dementia at the highest doses, especially in female patients, showing a dose-response relationship.
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spelling pubmed-90177652022-04-20 Benzodiazepine and Z-Drug Use and the Risk of Developing Dementia Torres-Bondia, Francisco Dakterzada, Farida Galván, Leonardo Buti, Miquel Besanson, Gaston Grill, Eric Buil, Roman de Batlle, Jordi Piñol-Ripoll, Gerard Int J Neuropsychopharmacol Regular Research Articles BACKGROUND: Benzodiazepines (BZDs) and Z-drugs (BZDRs) are among the most prescribed medications for anxiety and insomnia, especially among older adults. Our objective was to investigate the association between the use of BZDRs and the risk of dementia. METHODS: A community-based retrospective cohort study was conducted based on the data available from 2002 to 2015 in Catalan Health Service. This cohort included all BZDR users (N = 83 138) and nonusers (N = 84 652) older than 45 years. A minimum 5-year lag window and an adjustment for psychiatric problems were applied for the data analysis. RESULTS: The hazard ratio (HR) for the risk of incident dementia among BZDR users was 1.22 (95% CI = 1.15 to 1.31). This risk was not significant after adjusting the data confounding factors (HR = 1.01; 95% CI = 0.94 to 1.08). We observed a higher risk with short-to-intermediate half-life BZDs (HR = 1.11; 95% CI = 1.04 to 1.20) and Z-drugs (HR = 1.20; 95% CI = 1.07 to 1.33) than for intermediate-to-long half-life BZDs (HR = 1.01; 95% CI = 0.94 to 1.08). We demonstrated a higher risk of incident dementia (HR = 1.23; 95% CI = 1.07 to 1.41 and odds ratio = 1.38; 95% CI = 1.27 to 1.50, respectively) in patients who received 91 to 180 defined daily doses (DDDs) and >180 DDDs compared with patients who received <90 DDD. Regarding patient sex, the risk of dementia was higher in women than in men. CONCLUSION: We found that the incidence of dementia was not higher among all BZDR users. Short half-life BZDs and Z-drugs increased the risk of dementia at the highest doses, especially in female patients, showing a dose-response relationship. Oxford University Press 2021-11-02 /pmc/articles/PMC9017765/ /pubmed/34727174 http://dx.doi.org/10.1093/ijnp/pyab073 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of CINP. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Research Articles
Torres-Bondia, Francisco
Dakterzada, Farida
Galván, Leonardo
Buti, Miquel
Besanson, Gaston
Grill, Eric
Buil, Roman
de Batlle, Jordi
Piñol-Ripoll, Gerard
Benzodiazepine and Z-Drug Use and the Risk of Developing Dementia
title Benzodiazepine and Z-Drug Use and the Risk of Developing Dementia
title_full Benzodiazepine and Z-Drug Use and the Risk of Developing Dementia
title_fullStr Benzodiazepine and Z-Drug Use and the Risk of Developing Dementia
title_full_unstemmed Benzodiazepine and Z-Drug Use and the Risk of Developing Dementia
title_short Benzodiazepine and Z-Drug Use and the Risk of Developing Dementia
title_sort benzodiazepine and z-drug use and the risk of developing dementia
topic Regular Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017765/
https://www.ncbi.nlm.nih.gov/pubmed/34727174
http://dx.doi.org/10.1093/ijnp/pyab073
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