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Clinically significant anxiety as a risk factor for Alzheimer's disease: Results from a 10‐year follow‐up community study

OBJECTIVE: There is growing evidence for an association between anxiety and an increased risk of dementia, but it is not clear whether anxiety is a risk factor or a prodromic symptom. In this study, we investigated if clinically significant anxiety increases the risk of developing Alzheimer's d...

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Autores principales: Gracia‐García, Patricia, Bueno‐Notivol, Juan, Lipnicki, Darren M., de la Cámara, Concepción, Lobo, Antonio, Santabárbara, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485344/
https://www.ncbi.nlm.nih.gov/pubmed/36597404
http://dx.doi.org/10.1002/mpr.1934
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author Gracia‐García, Patricia
Bueno‐Notivol, Juan
Lipnicki, Darren M.
de la Cámara, Concepción
Lobo, Antonio
Santabárbara, Javier
author_facet Gracia‐García, Patricia
Bueno‐Notivol, Juan
Lipnicki, Darren M.
de la Cámara, Concepción
Lobo, Antonio
Santabárbara, Javier
author_sort Gracia‐García, Patricia
collection PubMed
description OBJECTIVE: There is growing evidence for an association between anxiety and an increased risk of dementia, but it is not clear whether anxiety is a risk factor or a prodromic symptom. In this study, we investigated if clinically significant anxiety increases the risk of developing Alzheimer's disease (AD) up to 10 years later. METHODS: We used data from the longitudinal Zaragoza Dementia and Depression (ZARADEMP) Project. Excluding subjects with dementia at baseline left us with 3044 individuals aged >65 years. The Geriatric Mental State‐Automated Geriatric Examination for Computer Assisted Taxonomy (GMS‐AGECAT) package was used to identify cases and subcases of anxiety. AD was diagnosed by a panel of research psychiatrists according to the Diagnostic and Statistical Manual of Mental Disorders, fourth edition (DSM‐IV) criteria. Multivariate survival analysis with a competing risk regression model was performed. RESULTS: We observed a significant association between clinically significant anxiety at baseline and AD risk within a 10‐year follow‐up (SHR 2.82 [95% CI 1.21–6.58]), after controlling for confounders including depression. In contrast, isolated symptoms of anxiety were not significantly associated with an increased incidence of AD. CONCLUSION: Our results support the hypothesis that clinically significant anxiety is an independent risk factor for AD and not just a prodromic symptom. Future studies should clarify if treating anxiety reduces the incidence of AD.
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spelling pubmed-104853442023-09-09 Clinically significant anxiety as a risk factor for Alzheimer's disease: Results from a 10‐year follow‐up community study Gracia‐García, Patricia Bueno‐Notivol, Juan Lipnicki, Darren M. de la Cámara, Concepción Lobo, Antonio Santabárbara, Javier Int J Methods Psychiatr Res Original Articles OBJECTIVE: There is growing evidence for an association between anxiety and an increased risk of dementia, but it is not clear whether anxiety is a risk factor or a prodromic symptom. In this study, we investigated if clinically significant anxiety increases the risk of developing Alzheimer's disease (AD) up to 10 years later. METHODS: We used data from the longitudinal Zaragoza Dementia and Depression (ZARADEMP) Project. Excluding subjects with dementia at baseline left us with 3044 individuals aged >65 years. The Geriatric Mental State‐Automated Geriatric Examination for Computer Assisted Taxonomy (GMS‐AGECAT) package was used to identify cases and subcases of anxiety. AD was diagnosed by a panel of research psychiatrists according to the Diagnostic and Statistical Manual of Mental Disorders, fourth edition (DSM‐IV) criteria. Multivariate survival analysis with a competing risk regression model was performed. RESULTS: We observed a significant association between clinically significant anxiety at baseline and AD risk within a 10‐year follow‐up (SHR 2.82 [95% CI 1.21–6.58]), after controlling for confounders including depression. In contrast, isolated symptoms of anxiety were not significantly associated with an increased incidence of AD. CONCLUSION: Our results support the hypothesis that clinically significant anxiety is an independent risk factor for AD and not just a prodromic symptom. Future studies should clarify if treating anxiety reduces the incidence of AD. John Wiley and Sons Inc. 2023-01-03 /pmc/articles/PMC10485344/ /pubmed/36597404 http://dx.doi.org/10.1002/mpr.1934 Text en © 2022 The Authors. International Journal of Methods in Psychiatric Research published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Gracia‐García, Patricia
Bueno‐Notivol, Juan
Lipnicki, Darren M.
de la Cámara, Concepción
Lobo, Antonio
Santabárbara, Javier
Clinically significant anxiety as a risk factor for Alzheimer's disease: Results from a 10‐year follow‐up community study
title Clinically significant anxiety as a risk factor for Alzheimer's disease: Results from a 10‐year follow‐up community study
title_full Clinically significant anxiety as a risk factor for Alzheimer's disease: Results from a 10‐year follow‐up community study
title_fullStr Clinically significant anxiety as a risk factor for Alzheimer's disease: Results from a 10‐year follow‐up community study
title_full_unstemmed Clinically significant anxiety as a risk factor for Alzheimer's disease: Results from a 10‐year follow‐up community study
title_short Clinically significant anxiety as a risk factor for Alzheimer's disease: Results from a 10‐year follow‐up community study
title_sort clinically significant anxiety as a risk factor for alzheimer's disease: results from a 10‐year follow‐up community study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485344/
https://www.ncbi.nlm.nih.gov/pubmed/36597404
http://dx.doi.org/10.1002/mpr.1934
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