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Antiherpetic drugs: a potential way to prevent Alzheimer’s disease?

BACKGROUND: Considering the growing body of evidence suggesting a potential implication of herpesviruses in the development of dementia, several authors have questioned a protective effect of antiherpetic drugs (AHDs) which may represent a new means of prevention, well tolerated and easily accessibl...

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Autores principales: Linard, Morgane, Bezin, Julien, Hucteau, Emilie, Joly, Pierre, Garrigue, Isabelle, Dartigues, Jean-François, Pariente, Antoine, Helmer, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742322/
https://www.ncbi.nlm.nih.gov/pubmed/34996520
http://dx.doi.org/10.1186/s13195-021-00950-0
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author Linard, Morgane
Bezin, Julien
Hucteau, Emilie
Joly, Pierre
Garrigue, Isabelle
Dartigues, Jean-François
Pariente, Antoine
Helmer, Catherine
author_facet Linard, Morgane
Bezin, Julien
Hucteau, Emilie
Joly, Pierre
Garrigue, Isabelle
Dartigues, Jean-François
Pariente, Antoine
Helmer, Catherine
author_sort Linard, Morgane
collection PubMed
description BACKGROUND: Considering the growing body of evidence suggesting a potential implication of herpesviruses in the development of dementia, several authors have questioned a protective effect of antiherpetic drugs (AHDs) which may represent a new means of prevention, well tolerated and easily accessible. Subsequently, several epidemiological studies have shown a reduction in the risk of dementia in subjects treated with AHDs, but the biological plausibility of this association and the impact of potential methodological biases need to be discussed in more depth. METHODS: Using a French medico-administrative database, we assessed the association between the intake of systemic AHDs and the incidence of (i) dementia, (ii) Alzheimer’s disease (AD), and (iii) vascular dementia in 68,291 subjects over 65 who were followed between 2009 and 2017. Regarding potential methodological biases, Cox models were adjusted for numerous potential confounding factors (including proxies of sociodemographic status, comorbidities, and use of healthcare) and sensitivity analyses were performed in an attempt to limit the risk of indication and reverse causality biases. RESULTS: 9.7% of subjects (n=6642) had at least one intake of systemic AHD, and 8883 incident cases of dementia were identified. Intake of at least one systemic AHD during follow-up was significantly associated with a decreased risk of AD (aHR 0.85 95% confidence interval [0.75–0.96], p=0.009) and, to a lesser extent with respect to p values, to both dementia from any cause and vascular dementia. The association with AD remained significant in sensitivity analyses. The number of subjects with a regular intake was low and prevented us from studying its association with dementia. CONCLUSIONS: Taking at least one systemic AHD during follow-up was significantly associated with a 15% reduced risk of developing AD, even after taking into account several potential methodological biases. Nevertheless, the low frequency of subjects with a regular intake questions the biological plausibility of this association and highlights the limits of epidemiological data to evaluate a potential protective effect of a regular treatment by systemic AHDs on the incidence of dementia SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-021-00950-0.
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spelling pubmed-87423222022-01-10 Antiherpetic drugs: a potential way to prevent Alzheimer’s disease? Linard, Morgane Bezin, Julien Hucteau, Emilie Joly, Pierre Garrigue, Isabelle Dartigues, Jean-François Pariente, Antoine Helmer, Catherine Alzheimers Res Ther Research BACKGROUND: Considering the growing body of evidence suggesting a potential implication of herpesviruses in the development of dementia, several authors have questioned a protective effect of antiherpetic drugs (AHDs) which may represent a new means of prevention, well tolerated and easily accessible. Subsequently, several epidemiological studies have shown a reduction in the risk of dementia in subjects treated with AHDs, but the biological plausibility of this association and the impact of potential methodological biases need to be discussed in more depth. METHODS: Using a French medico-administrative database, we assessed the association between the intake of systemic AHDs and the incidence of (i) dementia, (ii) Alzheimer’s disease (AD), and (iii) vascular dementia in 68,291 subjects over 65 who were followed between 2009 and 2017. Regarding potential methodological biases, Cox models were adjusted for numerous potential confounding factors (including proxies of sociodemographic status, comorbidities, and use of healthcare) and sensitivity analyses were performed in an attempt to limit the risk of indication and reverse causality biases. RESULTS: 9.7% of subjects (n=6642) had at least one intake of systemic AHD, and 8883 incident cases of dementia were identified. Intake of at least one systemic AHD during follow-up was significantly associated with a decreased risk of AD (aHR 0.85 95% confidence interval [0.75–0.96], p=0.009) and, to a lesser extent with respect to p values, to both dementia from any cause and vascular dementia. The association with AD remained significant in sensitivity analyses. The number of subjects with a regular intake was low and prevented us from studying its association with dementia. CONCLUSIONS: Taking at least one systemic AHD during follow-up was significantly associated with a 15% reduced risk of developing AD, even after taking into account several potential methodological biases. Nevertheless, the low frequency of subjects with a regular intake questions the biological plausibility of this association and highlights the limits of epidemiological data to evaluate a potential protective effect of a regular treatment by systemic AHDs on the incidence of dementia SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-021-00950-0. BioMed Central 2022-01-07 /pmc/articles/PMC8742322/ /pubmed/34996520 http://dx.doi.org/10.1186/s13195-021-00950-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Linard, Morgane
Bezin, Julien
Hucteau, Emilie
Joly, Pierre
Garrigue, Isabelle
Dartigues, Jean-François
Pariente, Antoine
Helmer, Catherine
Antiherpetic drugs: a potential way to prevent Alzheimer’s disease?
title Antiherpetic drugs: a potential way to prevent Alzheimer’s disease?
title_full Antiherpetic drugs: a potential way to prevent Alzheimer’s disease?
title_fullStr Antiherpetic drugs: a potential way to prevent Alzheimer’s disease?
title_full_unstemmed Antiherpetic drugs: a potential way to prevent Alzheimer’s disease?
title_short Antiherpetic drugs: a potential way to prevent Alzheimer’s disease?
title_sort antiherpetic drugs: a potential way to prevent alzheimer’s disease?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742322/
https://www.ncbi.nlm.nih.gov/pubmed/34996520
http://dx.doi.org/10.1186/s13195-021-00950-0
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