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dc.contributor.authorTorres-Bondia, Francisco-Ignacio-
dc.contributor.authorDakterzada, Farida-
dc.contributor.authorGalván, Leonardo-
dc.contributor.authorButi, Miquel -
dc.contributor.authorBesanson, Gaston -
dc.contributor.authorGrill, Eric-
dc.contributor.authorBuil Giné, Roman-
dc.contributor.authorde Batlle, Jordi-
dc.contributor.authorPiñol-Ripol, Gerard -
dc.contributor.otherUniversitat Oberta de Catalunya (UOC)-
dc.contributor.otherSanta Maria University Hospital-
dc.contributor.otherInstitut Català de la Salut-
dc.date.accessioned2022-10-18T07:18:51Z-
dc.date.available2022-10-18T07:18:51Z-
dc.date.issued2022-04-02-
dc.identifier.citationFrancisco Torres-Bondia, Farida Dakterzada, Leonardo Galván, Miquel Buti, Gaston Besanson, Eric Grill, Roman Buil, Jordi de Batlle, Gerard Piñol-Ripoll, Benzodiazepine and Z-Drug Use and the Risk of Developing Dementia, International Journal of Neuropsychopharmacology, Volume 25, Issue 4, April 2022, Pages 261–268, https://doi.org/10.1093/ijnp/pyab073-
dc.identifier.issn1461-1457MIAR
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dc.identifier.urihttp://hdl.handle.net/10609/146896-
dc.description.abstractBackground: 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.en
dc.format.mimetypeapplication/pdf-
dc.language.isoengca
dc.publisherInternational Journal of Neuropsychopharmacologyca
dc.relation.ispartofInternational Journal of Neuropsychopharmacology, 2022, 25(4)-
dc.relation.ispartofseries25;4-
dc.relation.urihttps://doi.org/10.1093/ijnp/pyab073-
dc.rightshttp://creativecommons.org/licenses/by-nc/4.0-
dc.rightsCC BY-NC 4.0-
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0-
dc.subjectalzheimer’s diseaseen
dc.subjectbenzodiazepineen
dc.subjectcognitive declineen
dc.subjectZ-drugen
dc.subjectenfermetat de l'alzheimerca
dc.subjectbenzodiacepinaca
dc.subjectdeteriorament cognitiuca
dc.subjectdroga-zca
dc.subjectenfermedad del alzheimeres
dc.subjectbenzodiacepinaes
dc.subject.lcshbenzodiazepinesen
dc.titleBenzodiazepine and Z-drug use and the risk of developing dementiaca
dc.typeinfo:eu-repo/semantics/articleca
dc.subject.lemacbenzodiazepinesca
dc.subject.lcshesbenzodiacepinases
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.doihttps://doi.org/10.1093/ijnp/pyab073-
dc.gir.idAR/0000009633-
dc.type.versioninfo:eu-repo/semantics/publishedVersion-
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