Aquaporin-4 cerebrospinal fluid levels are higher in neurodegenerative dementia: looking at glymphatic system dysregulation.


Journal

Alzheimer's research & therapy
ISSN: 1758-9193
Titre abrégé: Alzheimers Res Ther
Pays: England
ID NLM: 101511643

Informations de publication

Date de publication:
17 09 2022
Historique:
received: 19 02 2022
accepted: 04 09 2022
entrez: 17 9 2022
pubmed: 18 9 2022
medline: 21 9 2022
Statut: epublish

Résumé

Aquaporin-4 (AQP4) is a channel protein that plays a fundamental role in glymphatic system, a newly described pathway for fluid exchange in the central nervous system, as well as a central figure in a fascinating new theory for the pathophysiology of neurodegenerative diseases such as Alzheimer's disease (AD) and frontotemporal dementia (FTD). In this study, cerebrospinal fluid (CSF) concentration of AQP4, amyloid-β, total tau and P-tau were determined in 103 CSF samples from patients affected by neurodegenerative dementias (AD and FTD) or psychiatric diseases and 21 controls. Significantly higher levels of AQP4 were found in AD and FTD patients compared to subjects not affected by neurodegenerative diseases, and a significant, positive correlation between AQP4 and total tau levels was found. This evidence may pave the way for future studies focused on the role of this channel protein in the clinical assessment of the glymphatic function and degree of neurodegeneration.

Identifiants

pubmed: 36115967
doi: 10.1186/s13195-022-01077-6
pii: 10.1186/s13195-022-01077-6
pmc: PMC9482276
doi:

Substances chimiques

AQP4 protein, human 0
Aquaporin 4 0
tau Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

135

Informations de copyright

© 2022. The Author(s).

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Auteurs

Andrea Arighi (A)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurodegenerative Disease Unit, via Francesco Sforza 35, 20122, Milan, Italy. andrea.arighi@policlinico.mi.it.

Marina Arcaro (M)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurodegenerative Disease Unit, via Francesco Sforza 35, 20122, Milan, Italy.

Giorgio Giulio Fumagalli (GG)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurodegenerative Disease Unit, via Francesco Sforza 35, 20122, Milan, Italy.

Tiziana Carandini (T)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurodegenerative Disease Unit, via Francesco Sforza 35, 20122, Milan, Italy.

Anna Margherita Pietroboni (AM)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurodegenerative Disease Unit, via Francesco Sforza 35, 20122, Milan, Italy.

Luca Sacchi (L)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurodegenerative Disease Unit, via Francesco Sforza 35, 20122, Milan, Italy.
University of Milan, Milan, Italy.

Chiara Fenoglio (C)

University of Milan, Milan, Italy.

Maria Serpente (M)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurodegenerative Disease Unit, via Francesco Sforza 35, 20122, Milan, Italy.

Federica Sorrentino (F)

University of Milan, Milan, Italy.

Giovanni Isgrò (G)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurodegenerative Disease Unit, via Francesco Sforza 35, 20122, Milan, Italy.

Federico Turkheimer (F)

Department of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

Elio Scarpini (E)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurodegenerative Disease Unit, via Francesco Sforza 35, 20122, Milan, Italy.
University of Milan, Milan, Italy.

Daniela Galimberti (D)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurodegenerative Disease Unit, via Francesco Sforza 35, 20122, Milan, Italy.
University of Milan, Milan, Italy.

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