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Cerebrospinal Fluid EV Concentration and Size Are Altered in Alzheimer’s Disease and Dementia with Lewy Bodies

Alzheimer’s disease (AD), dementia with Lewy bodies (DLB) and frontotemporal dementia (FTD) represent the three major neurodegenerative dementias characterized by abnormal brain protein accumulation. In this study, we investigated extracellular vesicles (EVs) and neurotrophic factors in the cerebros...

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Autores principales: Longobardi, Antonio, Nicsanu, Roland, Bellini, Sonia, Squitti, Rosanna, Catania, Marcella, Tiraboschi, Pietro, Saraceno, Claudia, Ferrari, Clarissa, Zanardini, Roberta, Binetti, Giuliano, Di Fede, Giuseppe, Benussi, Luisa, Ghidoni, Roberta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8834088/
https://www.ncbi.nlm.nih.gov/pubmed/35159272
http://dx.doi.org/10.3390/cells11030462
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author Longobardi, Antonio
Nicsanu, Roland
Bellini, Sonia
Squitti, Rosanna
Catania, Marcella
Tiraboschi, Pietro
Saraceno, Claudia
Ferrari, Clarissa
Zanardini, Roberta
Binetti, Giuliano
Di Fede, Giuseppe
Benussi, Luisa
Ghidoni, Roberta
author_facet Longobardi, Antonio
Nicsanu, Roland
Bellini, Sonia
Squitti, Rosanna
Catania, Marcella
Tiraboschi, Pietro
Saraceno, Claudia
Ferrari, Clarissa
Zanardini, Roberta
Binetti, Giuliano
Di Fede, Giuseppe
Benussi, Luisa
Ghidoni, Roberta
author_sort Longobardi, Antonio
collection PubMed
description Alzheimer’s disease (AD), dementia with Lewy bodies (DLB) and frontotemporal dementia (FTD) represent the three major neurodegenerative dementias characterized by abnormal brain protein accumulation. In this study, we investigated extracellular vesicles (EVs) and neurotrophic factors in the cerebrospinal fluid (CSF) of 120 subjects: 36 with AD, 30 with DLB, 34 with FTD and 20 controls. Specifically, CSF EVs were analyzed by Nanoparticle Tracking Analysis and neurotrophic factors were measured with ELISA. We found higher EV concentration and lower EV size in AD and DLB groups compared to the controls. Classification tree analysis demonstrated EV size as the best parameter able to discriminate the patients from the controls (96.7% vs. 3.3%, respectively). The diagnostic performance of the EV concentration/size ratio resulted in a fair discrimination level with an area under the curve of 0.74. Moreover, the EV concentration/size ratio was associated with the p-Tau181/Aβ42 ratio in AD patients. In addition, we described altered levels of cystatin C and progranulin in the DLB and AD groups. We did not find any correlation between neurotrophic factors and EV parameters. In conclusion, the results of this study suggest a common involvement of the endosomal pathway in neurodegenerative dementias, giving important insight into the molecular mechanisms underlying these pathologies.
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spelling pubmed-88340882022-02-12 Cerebrospinal Fluid EV Concentration and Size Are Altered in Alzheimer’s Disease and Dementia with Lewy Bodies Longobardi, Antonio Nicsanu, Roland Bellini, Sonia Squitti, Rosanna Catania, Marcella Tiraboschi, Pietro Saraceno, Claudia Ferrari, Clarissa Zanardini, Roberta Binetti, Giuliano Di Fede, Giuseppe Benussi, Luisa Ghidoni, Roberta Cells Article Alzheimer’s disease (AD), dementia with Lewy bodies (DLB) and frontotemporal dementia (FTD) represent the three major neurodegenerative dementias characterized by abnormal brain protein accumulation. In this study, we investigated extracellular vesicles (EVs) and neurotrophic factors in the cerebrospinal fluid (CSF) of 120 subjects: 36 with AD, 30 with DLB, 34 with FTD and 20 controls. Specifically, CSF EVs were analyzed by Nanoparticle Tracking Analysis and neurotrophic factors were measured with ELISA. We found higher EV concentration and lower EV size in AD and DLB groups compared to the controls. Classification tree analysis demonstrated EV size as the best parameter able to discriminate the patients from the controls (96.7% vs. 3.3%, respectively). The diagnostic performance of the EV concentration/size ratio resulted in a fair discrimination level with an area under the curve of 0.74. Moreover, the EV concentration/size ratio was associated with the p-Tau181/Aβ42 ratio in AD patients. In addition, we described altered levels of cystatin C and progranulin in the DLB and AD groups. We did not find any correlation between neurotrophic factors and EV parameters. In conclusion, the results of this study suggest a common involvement of the endosomal pathway in neurodegenerative dementias, giving important insight into the molecular mechanisms underlying these pathologies. MDPI 2022-01-28 /pmc/articles/PMC8834088/ /pubmed/35159272 http://dx.doi.org/10.3390/cells11030462 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Longobardi, Antonio
Nicsanu, Roland
Bellini, Sonia
Squitti, Rosanna
Catania, Marcella
Tiraboschi, Pietro
Saraceno, Claudia
Ferrari, Clarissa
Zanardini, Roberta
Binetti, Giuliano
Di Fede, Giuseppe
Benussi, Luisa
Ghidoni, Roberta
Cerebrospinal Fluid EV Concentration and Size Are Altered in Alzheimer’s Disease and Dementia with Lewy Bodies
title Cerebrospinal Fluid EV Concentration and Size Are Altered in Alzheimer’s Disease and Dementia with Lewy Bodies
title_full Cerebrospinal Fluid EV Concentration and Size Are Altered in Alzheimer’s Disease and Dementia with Lewy Bodies
title_fullStr Cerebrospinal Fluid EV Concentration and Size Are Altered in Alzheimer’s Disease and Dementia with Lewy Bodies
title_full_unstemmed Cerebrospinal Fluid EV Concentration and Size Are Altered in Alzheimer’s Disease and Dementia with Lewy Bodies
title_short Cerebrospinal Fluid EV Concentration and Size Are Altered in Alzheimer’s Disease and Dementia with Lewy Bodies
title_sort cerebrospinal fluid ev concentration and size are altered in alzheimer’s disease and dementia with lewy bodies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8834088/
https://www.ncbi.nlm.nih.gov/pubmed/35159272
http://dx.doi.org/10.3390/cells11030462
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