Cargando…

Comorbidity between Alzheimer’s disease and major depression: a behavioural and transcriptomic characterization study in mice

BACKGROUND: Major depression (MD) is the most prevalent psychiatric disease in the population and is considered a prodromal stage of the Alzheimer’s disease (AD). Despite both diseases having a robust genetic component, the common transcriptomic signature remains unknown. METHODS: We investigated th...

Descripción completa

Detalles Bibliográficos
Autores principales: Martín-Sánchez, Ana, Piñero, Janet, Nonell, Lara, Arnal, Magdalena, Ribe, Elena M., Nevado-Holgado, Alejo, Lovestone, Simon, Sanz, Ferran, Furlong, Laura I., Valverde, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017643/
https://www.ncbi.nlm.nih.gov/pubmed/33795014
http://dx.doi.org/10.1186/s13195-021-00810-x
_version_ 1783674090360406016
author Martín-Sánchez, Ana
Piñero, Janet
Nonell, Lara
Arnal, Magdalena
Ribe, Elena M.
Nevado-Holgado, Alejo
Lovestone, Simon
Sanz, Ferran
Furlong, Laura I.
Valverde, Olga
author_facet Martín-Sánchez, Ana
Piñero, Janet
Nonell, Lara
Arnal, Magdalena
Ribe, Elena M.
Nevado-Holgado, Alejo
Lovestone, Simon
Sanz, Ferran
Furlong, Laura I.
Valverde, Olga
author_sort Martín-Sánchez, Ana
collection PubMed
description BACKGROUND: Major depression (MD) is the most prevalent psychiatric disease in the population and is considered a prodromal stage of the Alzheimer’s disease (AD). Despite both diseases having a robust genetic component, the common transcriptomic signature remains unknown. METHODS: We investigated the cognitive and emotional behavioural responses in 3- and 6-month-old APP/PSEN1-Tg mice, before β-amyloid plaques were detected. We studied the genetic and pathway deregulation in the prefrontal cortex, striatum, hippocampus and amygdala of mice at both ages, using transcriptomic and functional data analysis. RESULTS: We found that depressive-like and anxiety-like behaviours, as well as memory impairments, are already present at 3-month-old APP/PSEN1-Tg mutant mice together with the deregulation of several genes, such as Ciart, Grin3b, Nr1d1 and Mc4r, and other genes including components of the circadian rhythms, electron transport chain and neurotransmission in all brain areas. Extending these results to human data performing GSEA analysis using DisGeNET database, it provides translational support for common deregulated gene sets related to MD and AD. CONCLUSIONS: The present study sheds light on the shared genetic bases between MD and AD, based on a comprehensive characterization from the behavioural to transcriptomic level. These findings suggest that late MD could be an early manifestation of AD.
format Online
Article
Text
id pubmed-8017643
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-80176432021-04-02 Comorbidity between Alzheimer’s disease and major depression: a behavioural and transcriptomic characterization study in mice Martín-Sánchez, Ana Piñero, Janet Nonell, Lara Arnal, Magdalena Ribe, Elena M. Nevado-Holgado, Alejo Lovestone, Simon Sanz, Ferran Furlong, Laura I. Valverde, Olga Alzheimers Res Ther Research BACKGROUND: Major depression (MD) is the most prevalent psychiatric disease in the population and is considered a prodromal stage of the Alzheimer’s disease (AD). Despite both diseases having a robust genetic component, the common transcriptomic signature remains unknown. METHODS: We investigated the cognitive and emotional behavioural responses in 3- and 6-month-old APP/PSEN1-Tg mice, before β-amyloid plaques were detected. We studied the genetic and pathway deregulation in the prefrontal cortex, striatum, hippocampus and amygdala of mice at both ages, using transcriptomic and functional data analysis. RESULTS: We found that depressive-like and anxiety-like behaviours, as well as memory impairments, are already present at 3-month-old APP/PSEN1-Tg mutant mice together with the deregulation of several genes, such as Ciart, Grin3b, Nr1d1 and Mc4r, and other genes including components of the circadian rhythms, electron transport chain and neurotransmission in all brain areas. Extending these results to human data performing GSEA analysis using DisGeNET database, it provides translational support for common deregulated gene sets related to MD and AD. CONCLUSIONS: The present study sheds light on the shared genetic bases between MD and AD, based on a comprehensive characterization from the behavioural to transcriptomic level. These findings suggest that late MD could be an early manifestation of AD. BioMed Central 2021-04-02 /pmc/articles/PMC8017643/ /pubmed/33795014 http://dx.doi.org/10.1186/s13195-021-00810-x Text en © The Author(s) 2021 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/. 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 in a credit line to the data.
spellingShingle Research
Martín-Sánchez, Ana
Piñero, Janet
Nonell, Lara
Arnal, Magdalena
Ribe, Elena M.
Nevado-Holgado, Alejo
Lovestone, Simon
Sanz, Ferran
Furlong, Laura I.
Valverde, Olga
Comorbidity between Alzheimer’s disease and major depression: a behavioural and transcriptomic characterization study in mice
title Comorbidity between Alzheimer’s disease and major depression: a behavioural and transcriptomic characterization study in mice
title_full Comorbidity between Alzheimer’s disease and major depression: a behavioural and transcriptomic characterization study in mice
title_fullStr Comorbidity between Alzheimer’s disease and major depression: a behavioural and transcriptomic characterization study in mice
title_full_unstemmed Comorbidity between Alzheimer’s disease and major depression: a behavioural and transcriptomic characterization study in mice
title_short Comorbidity between Alzheimer’s disease and major depression: a behavioural and transcriptomic characterization study in mice
title_sort comorbidity between alzheimer’s disease and major depression: a behavioural and transcriptomic characterization study in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017643/
https://www.ncbi.nlm.nih.gov/pubmed/33795014
http://dx.doi.org/10.1186/s13195-021-00810-x
work_keys_str_mv AT martinsanchezana comorbiditybetweenalzheimersdiseaseandmajordepressionabehaviouralandtranscriptomiccharacterizationstudyinmice
AT pinerojanet comorbiditybetweenalzheimersdiseaseandmajordepressionabehaviouralandtranscriptomiccharacterizationstudyinmice
AT nonelllara comorbiditybetweenalzheimersdiseaseandmajordepressionabehaviouralandtranscriptomiccharacterizationstudyinmice
AT arnalmagdalena comorbiditybetweenalzheimersdiseaseandmajordepressionabehaviouralandtranscriptomiccharacterizationstudyinmice
AT ribeelenam comorbiditybetweenalzheimersdiseaseandmajordepressionabehaviouralandtranscriptomiccharacterizationstudyinmice
AT nevadoholgadoalejo comorbiditybetweenalzheimersdiseaseandmajordepressionabehaviouralandtranscriptomiccharacterizationstudyinmice
AT lovestonesimon comorbiditybetweenalzheimersdiseaseandmajordepressionabehaviouralandtranscriptomiccharacterizationstudyinmice
AT sanzferran comorbiditybetweenalzheimersdiseaseandmajordepressionabehaviouralandtranscriptomiccharacterizationstudyinmice
AT furlonglaurai comorbiditybetweenalzheimersdiseaseandmajordepressionabehaviouralandtranscriptomiccharacterizationstudyinmice
AT valverdeolga comorbiditybetweenalzheimersdiseaseandmajordepressionabehaviouralandtranscriptomiccharacterizationstudyinmice