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Hydroxytryptamine transporter gene-linked polymorphic region (5HTTLPR) is associated with delusions in Alzheimer’s disease

BACKGROUND: Serotoninergic pathways underlying delusion symptoms in Alzheimer’s disease (AD) have not been fully clarified. 5-Hydroxytryptamine transporter gene-linked polymorphic region (5-HTTLPR) is a variable number tandem repeats in the promoter region of serotonin transporter encoding-gene affe...

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Autores principales: D’Onofrio, Grazia, Panza, Francesco, Sancarlo, Daniele, Lauriola, Michele, Dagostino, Mariangela P., Paroni, Giulia, Lozupone, Madia, Mangiacotti, Antonio, Bisceglia, Paola, Gravina, Carolina, Urbano, Maria, Addante, Filomena, Paris, Francesco, Cascavilla, Leandro, Greco, Antonio, Seripa, Davide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357440/
https://www.ncbi.nlm.nih.gov/pubmed/30733861
http://dx.doi.org/10.1186/s40035-019-0144-1
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author D’Onofrio, Grazia
Panza, Francesco
Sancarlo, Daniele
Lauriola, Michele
Dagostino, Mariangela P.
Paroni, Giulia
Lozupone, Madia
Mangiacotti, Antonio
Bisceglia, Paola
Gravina, Carolina
Urbano, Maria
Addante, Filomena
Paris, Francesco
Cascavilla, Leandro
Greco, Antonio
Seripa, Davide
author_facet D’Onofrio, Grazia
Panza, Francesco
Sancarlo, Daniele
Lauriola, Michele
Dagostino, Mariangela P.
Paroni, Giulia
Lozupone, Madia
Mangiacotti, Antonio
Bisceglia, Paola
Gravina, Carolina
Urbano, Maria
Addante, Filomena
Paris, Francesco
Cascavilla, Leandro
Greco, Antonio
Seripa, Davide
author_sort D’Onofrio, Grazia
collection PubMed
description BACKGROUND: Serotoninergic pathways underlying delusion symptoms in Alzheimer’s disease (AD) have not been fully clarified. 5-Hydroxytryptamine transporter gene-linked polymorphic region (5-HTTLPR) is a variable number tandem repeats in the promoter region of serotonin transporter encoding-gene affecting transcription. METHODS: We investigated the association of 5-HTTLPR with delusions in a total of 257 consecutive patients clinically diagnosed as AD according to the National Institute on Aging-Alzheimer’s Association criteria. All participants underwent a comprehensive evaluation with a standardized comprehensive geriatric assessment and Neuropsychiatric Inventory. RESULTS: Delusion symptoms were observed in 171 patients (66.54%). In respect to AD patients without delusions, AD patients with delusions showed a low prevalence of S-plus carriers (5-HTTLPR-L/S + 5-HTTLPR-S/S genotypes) [p < 0.001; odds ratio (OR) = 0.240, 95% confidence interval (CI) = 0.121–0.471]. Logistic regression analysis adjusted for the apolipoprotein E polymorphism showed that in AD patients with delusions the presence of an 5-HTTLPR-S allele may reduce disease duration (p = 0.005; OR = 0.680, 95% CI = 0.522–0.886) and increase aberrant motor activity (p = 0.013; OR = 2.257, 95% CI = 1.195–4.260). The present findings suggested that 5-HTTLPR might be associated with delusions in AD. S-plus carriers might be associated with protective effect against delusions in AD. CONCLUSIONS: More studies on wider samples of high selected demented patients are needed to confirm our results. However, the present findings suggested that a genetic factor related to serotonin metabolism might exert a protective role on the clinical expression of neuropsychiatric clusters in AD with important implications regarding mechanisms underlying delusions and their possible treatment across the AD and dementia spectrum. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40035-019-0144-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-63574402019-02-07 Hydroxytryptamine transporter gene-linked polymorphic region (5HTTLPR) is associated with delusions in Alzheimer’s disease D’Onofrio, Grazia Panza, Francesco Sancarlo, Daniele Lauriola, Michele Dagostino, Mariangela P. Paroni, Giulia Lozupone, Madia Mangiacotti, Antonio Bisceglia, Paola Gravina, Carolina Urbano, Maria Addante, Filomena Paris, Francesco Cascavilla, Leandro Greco, Antonio Seripa, Davide Transl Neurodegener Research BACKGROUND: Serotoninergic pathways underlying delusion symptoms in Alzheimer’s disease (AD) have not been fully clarified. 5-Hydroxytryptamine transporter gene-linked polymorphic region (5-HTTLPR) is a variable number tandem repeats in the promoter region of serotonin transporter encoding-gene affecting transcription. METHODS: We investigated the association of 5-HTTLPR with delusions in a total of 257 consecutive patients clinically diagnosed as AD according to the National Institute on Aging-Alzheimer’s Association criteria. All participants underwent a comprehensive evaluation with a standardized comprehensive geriatric assessment and Neuropsychiatric Inventory. RESULTS: Delusion symptoms were observed in 171 patients (66.54%). In respect to AD patients without delusions, AD patients with delusions showed a low prevalence of S-plus carriers (5-HTTLPR-L/S + 5-HTTLPR-S/S genotypes) [p < 0.001; odds ratio (OR) = 0.240, 95% confidence interval (CI) = 0.121–0.471]. Logistic regression analysis adjusted for the apolipoprotein E polymorphism showed that in AD patients with delusions the presence of an 5-HTTLPR-S allele may reduce disease duration (p = 0.005; OR = 0.680, 95% CI = 0.522–0.886) and increase aberrant motor activity (p = 0.013; OR = 2.257, 95% CI = 1.195–4.260). The present findings suggested that 5-HTTLPR might be associated with delusions in AD. S-plus carriers might be associated with protective effect against delusions in AD. CONCLUSIONS: More studies on wider samples of high selected demented patients are needed to confirm our results. However, the present findings suggested that a genetic factor related to serotonin metabolism might exert a protective role on the clinical expression of neuropsychiatric clusters in AD with important implications regarding mechanisms underlying delusions and their possible treatment across the AD and dementia spectrum. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40035-019-0144-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-01 /pmc/articles/PMC6357440/ /pubmed/30733861 http://dx.doi.org/10.1186/s40035-019-0144-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
D’Onofrio, Grazia
Panza, Francesco
Sancarlo, Daniele
Lauriola, Michele
Dagostino, Mariangela P.
Paroni, Giulia
Lozupone, Madia
Mangiacotti, Antonio
Bisceglia, Paola
Gravina, Carolina
Urbano, Maria
Addante, Filomena
Paris, Francesco
Cascavilla, Leandro
Greco, Antonio
Seripa, Davide
Hydroxytryptamine transporter gene-linked polymorphic region (5HTTLPR) is associated with delusions in Alzheimer’s disease
title Hydroxytryptamine transporter gene-linked polymorphic region (5HTTLPR) is associated with delusions in Alzheimer’s disease
title_full Hydroxytryptamine transporter gene-linked polymorphic region (5HTTLPR) is associated with delusions in Alzheimer’s disease
title_fullStr Hydroxytryptamine transporter gene-linked polymorphic region (5HTTLPR) is associated with delusions in Alzheimer’s disease
title_full_unstemmed Hydroxytryptamine transporter gene-linked polymorphic region (5HTTLPR) is associated with delusions in Alzheimer’s disease
title_short Hydroxytryptamine transporter gene-linked polymorphic region (5HTTLPR) is associated with delusions in Alzheimer’s disease
title_sort hydroxytryptamine transporter gene-linked polymorphic region (5httlpr) is associated with delusions in alzheimer’s disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357440/
https://www.ncbi.nlm.nih.gov/pubmed/30733861
http://dx.doi.org/10.1186/s40035-019-0144-1
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