Benzodiazepine use and the risk of dementia

Abstract Introduction Benzodiazepines (BZDs) are commonly prescribed for anxiety and agitations, which are early symptoms of Alzheimer's disease and related dementias (ADRD). It is unclear whether BZDs causally affect ADRD risk or are prescribed in response to early symptoms of dementia. Method...

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Main Authors: Geoffrey Joyce, Patricia Ferido, Johanna Thunell, Bryan Tysinger, Julie Zissimopoulos
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Alzheimer’s & Dementia: Translational Research & Clinical Interventions
Subjects:
Online Access:https://doi.org/10.1002/trc2.12309
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author Geoffrey Joyce
Patricia Ferido
Johanna Thunell
Bryan Tysinger
Julie Zissimopoulos
author_facet Geoffrey Joyce
Patricia Ferido
Johanna Thunell
Bryan Tysinger
Julie Zissimopoulos
author_sort Geoffrey Joyce
collection DOAJ
description Abstract Introduction Benzodiazepines (BZDs) are commonly prescribed for anxiety and agitations, which are early symptoms of Alzheimer's disease and related dementias (ADRD). It is unclear whether BZDs causally affect ADRD risk or are prescribed in response to early symptoms of dementia. Methods We replicate prior case‐control studies using longitudinal Medicare claims. To mitigate bias from prodromal use, we compare rates of ADRD diagnosis for beneficiaries exposed and unexposed to BZDs for cervical/lumbar pain, stenosis, and sciatica, none of which are associated with dementia. Results Approximately 8% of Medicare beneficiaries used a BZD in 2007, increasing to nearly 13% by 2013. Estimates from case‐control designs are sensitive to duration of look‐back period, health histories, medication use, and exclusion of decedents. Incident BZD use is not associated with an increased risk of dementia in an “uncontaminated” sample of beneficiaries prescribed a BZD for pain (odds ratios (ORs) of 1.007 [95% confidence interval [CI] = 0.885, 1.146] and 0.986 [95% CI = 0.877, 1.108], respectively, in the 2013 and 2013 to 2015 pooled samples). Higher levels of BZD exposure (>365 days over a 2‐year period) are associated with increased odds of a dementia diagnosis, but the results are not statistically significant at the 5% or 10% levels (1.190 [95% CI = 0.925, 1.531] and 1.167 [95% CI = 0.919, 1.483]). Discussion We find little evidence of a causal relation between BZD use and dementia risk. Nonetheless, providers should limit the extended use in elderly populations.
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spelling doaj.art-ffff1b60a5f34233be2e6960fdfe16402024-12-03T12:37:31ZengWileyAlzheimer’s & Dementia: Translational Research & Clinical Interventions2352-87372022-01-0181n/an/a10.1002/trc2.12309Benzodiazepine use and the risk of dementiaGeoffrey Joyce0Patricia Ferido1Johanna Thunell2Bryan Tysinger3Julie Zissimopoulos4University of Southern California (USC) Schaeffer Center for Health Policy and Economics Los Angeles CA Los Angeles CountyUniversity of Southern California (USC) Schaeffer Center for Health Policy and Economics Los Angeles CA Los Angeles CountyUniversity of Southern California (USC) Schaeffer Center for Health Policy and Economics Los Angeles CA Los Angeles CountyUniversity of Southern California (USC) Schaeffer Center for Health Policy and Economics Los Angeles CA Los Angeles CountyUniversity of Southern California (USC) Schaeffer Center for Health Policy and Economics Los Angeles CA Los Angeles CountyAbstract Introduction Benzodiazepines (BZDs) are commonly prescribed for anxiety and agitations, which are early symptoms of Alzheimer's disease and related dementias (ADRD). It is unclear whether BZDs causally affect ADRD risk or are prescribed in response to early symptoms of dementia. Methods We replicate prior case‐control studies using longitudinal Medicare claims. To mitigate bias from prodromal use, we compare rates of ADRD diagnosis for beneficiaries exposed and unexposed to BZDs for cervical/lumbar pain, stenosis, and sciatica, none of which are associated with dementia. Results Approximately 8% of Medicare beneficiaries used a BZD in 2007, increasing to nearly 13% by 2013. Estimates from case‐control designs are sensitive to duration of look‐back period, health histories, medication use, and exclusion of decedents. Incident BZD use is not associated with an increased risk of dementia in an “uncontaminated” sample of beneficiaries prescribed a BZD for pain (odds ratios (ORs) of 1.007 [95% confidence interval [CI] = 0.885, 1.146] and 0.986 [95% CI = 0.877, 1.108], respectively, in the 2013 and 2013 to 2015 pooled samples). Higher levels of BZD exposure (>365 days over a 2‐year period) are associated with increased odds of a dementia diagnosis, but the results are not statistically significant at the 5% or 10% levels (1.190 [95% CI = 0.925, 1.531] and 1.167 [95% CI = 0.919, 1.483]). Discussion We find little evidence of a causal relation between BZD use and dementia risk. Nonetheless, providers should limit the extended use in elderly populations.https://doi.org/10.1002/trc2.12309Benzodiazepinescase‐control designscausal estimatesdementia riskMedicare beneficiaries
spellingShingle Geoffrey Joyce
Patricia Ferido
Johanna Thunell
Bryan Tysinger
Julie Zissimopoulos
Benzodiazepine use and the risk of dementia
Alzheimer’s & Dementia: Translational Research & Clinical Interventions
Benzodiazepines
case‐control designs
causal estimates
dementia risk
Medicare beneficiaries
title Benzodiazepine use and the risk of dementia
title_full Benzodiazepine use and the risk of dementia
title_fullStr Benzodiazepine use and the risk of dementia
title_full_unstemmed Benzodiazepine use and the risk of dementia
title_short Benzodiazepine use and the risk of dementia
title_sort benzodiazepine use and the risk of dementia
topic Benzodiazepines
case‐control designs
causal estimates
dementia risk
Medicare beneficiaries
url https://doi.org/10.1002/trc2.12309
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AT johannathunell benzodiazepineuseandtheriskofdementia
AT bryantysinger benzodiazepineuseandtheriskofdementia
AT juliezissimopoulos benzodiazepineuseandtheriskofdementia