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Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect
Extracellular vesicles (EVs) are mediators of cellular communication that can be released by almost all cell types in both physiological and pathological conditions and are present in most biological fluids. Such characteristics make them attractive in the research of biomarkers for age-related path...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400496/ https://www.ncbi.nlm.nih.gov/pubmed/36725819 http://dx.doi.org/10.1007/s11357-023-00746-0 |
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author | Visconte, C. Golia, M.T. Fenoglio, C. Serpente, M. Gabrielli, M. Arcaro, M. Sorrentino, F. Busnelli, M. Arighi, A. Fumagalli, G. Rotondo, E. Rossi, P. Arosio, B. Scarpini, E. Verderio, C. Galimberti, D. |
author_facet | Visconte, C. Golia, M.T. Fenoglio, C. Serpente, M. Gabrielli, M. Arcaro, M. Sorrentino, F. Busnelli, M. Arighi, A. Fumagalli, G. Rotondo, E. Rossi, P. Arosio, B. Scarpini, E. Verderio, C. Galimberti, D. |
author_sort | Visconte, C. |
collection | PubMed |
description | Extracellular vesicles (EVs) are mediators of cellular communication that can be released by almost all cell types in both physiological and pathological conditions and are present in most biological fluids. Such characteristics make them attractive in the research of biomarkers for age-related pathological conditions. Based on this, the aim of the present study was to examine the changes in EV concentration and size in the context of frailty, a geriatric syndrome associated with a progressive physical and cognitive decline. Specifically, total EVs and neural and microglial-derived EVs (NDVs and MDVs respectively) were investigated in plasma of frail and non-frail controls (CTRL), mild cognitive impairment (MCI) subjects, and in Alzheimer’s disease (AD) patients. Results provided evidence that AD patients displayed diminished NDV concentration (3.61 × 10(9) ± 1.92 × 10(9) vs 7.16 × 10(9) ± 4.3 × 10(9) particles/ml) and showed high diagnostic performance. They are able to discriminate between AD and CTRL with an area under the curve of 0.80, a sensitivity of 78.95% and a specificity of 85.7%, considering the cut-off of 5.27 × 10(9) particles/ml. Importantly, we also found that MDV concentration was increased in frail MCI patients compared to CTRL (5.89 × 10(9) ± 3.98 × 10(9) vs 3.16 × 10(9) ± 3.04 × 10(9) particles/ml, P < 0.05) and showed high neurotoxic effect on neurons. MDV concentration discriminate frail MCI vs non-frail CTRL (AUC = 0.76) with a sensitivity of 80% and a specificity of 70%, considering the cut-off of 2.69 × 10(9) particles/ml. Altogether, these results demonstrated an alteration in NDV and MDV release during cognitive decline, providing important insight into the role of EVs in frailty status. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11357-023-00746-0. |
format | Online Article Text |
id | pubmed-10400496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-104004962023-08-05 Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect Visconte, C. Golia, M.T. Fenoglio, C. Serpente, M. Gabrielli, M. Arcaro, M. Sorrentino, F. Busnelli, M. Arighi, A. Fumagalli, G. Rotondo, E. Rossi, P. Arosio, B. Scarpini, E. Verderio, C. Galimberti, D. GeroScience Original Article Extracellular vesicles (EVs) are mediators of cellular communication that can be released by almost all cell types in both physiological and pathological conditions and are present in most biological fluids. Such characteristics make them attractive in the research of biomarkers for age-related pathological conditions. Based on this, the aim of the present study was to examine the changes in EV concentration and size in the context of frailty, a geriatric syndrome associated with a progressive physical and cognitive decline. Specifically, total EVs and neural and microglial-derived EVs (NDVs and MDVs respectively) were investigated in plasma of frail and non-frail controls (CTRL), mild cognitive impairment (MCI) subjects, and in Alzheimer’s disease (AD) patients. Results provided evidence that AD patients displayed diminished NDV concentration (3.61 × 10(9) ± 1.92 × 10(9) vs 7.16 × 10(9) ± 4.3 × 10(9) particles/ml) and showed high diagnostic performance. They are able to discriminate between AD and CTRL with an area under the curve of 0.80, a sensitivity of 78.95% and a specificity of 85.7%, considering the cut-off of 5.27 × 10(9) particles/ml. Importantly, we also found that MDV concentration was increased in frail MCI patients compared to CTRL (5.89 × 10(9) ± 3.98 × 10(9) vs 3.16 × 10(9) ± 3.04 × 10(9) particles/ml, P < 0.05) and showed high neurotoxic effect on neurons. MDV concentration discriminate frail MCI vs non-frail CTRL (AUC = 0.76) with a sensitivity of 80% and a specificity of 70%, considering the cut-off of 2.69 × 10(9) particles/ml. Altogether, these results demonstrated an alteration in NDV and MDV release during cognitive decline, providing important insight into the role of EVs in frailty status. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11357-023-00746-0. Springer International Publishing 2023-02-01 /pmc/articles/PMC10400496/ /pubmed/36725819 http://dx.doi.org/10.1007/s11357-023-00746-0 Text en © The Author(s) 2023 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/) . |
spellingShingle | Original Article Visconte, C. Golia, M.T. Fenoglio, C. Serpente, M. Gabrielli, M. Arcaro, M. Sorrentino, F. Busnelli, M. Arighi, A. Fumagalli, G. Rotondo, E. Rossi, P. Arosio, B. Scarpini, E. Verderio, C. Galimberti, D. Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect |
title | Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect |
title_full | Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect |
title_fullStr | Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect |
title_full_unstemmed | Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect |
title_short | Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect |
title_sort | plasma microglial-derived extracellular vesicles are increased in frail patients with mild cognitive impairment and exert a neurotoxic effect |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400496/ https://www.ncbi.nlm.nih.gov/pubmed/36725819 http://dx.doi.org/10.1007/s11357-023-00746-0 |
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