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Tau and Amyloid-β Peptides in Serum of Patients With Parkinson's Disease: Correlations With CSF Levels and Clinical Parameters

Relevance of blood-based biomarkers is increasing into the neurodegenerative diseases field, but data on Parkinson's disease (PD) remain still scarce. In this study, we used the SiMoA technique to measure serum content of total tau protein and amyloid-β peptides (Aβ-42, Aβ-40) in 22 PD patients...

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Autores principales: Schirinzi, Tommaso, Zenuni, Henri, Grillo, Piergiorgio, Bovenzi, Roberta, Guerrera, Gisella, Gargano, Francesca, Pieri, Massimo, Bernardini, Sergio, Biagio Mercuri, Nicola, Battistini, Luca, Sancesario, Giulia Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8914101/
https://www.ncbi.nlm.nih.gov/pubmed/35280296
http://dx.doi.org/10.3389/fneur.2022.748599
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author Schirinzi, Tommaso
Zenuni, Henri
Grillo, Piergiorgio
Bovenzi, Roberta
Guerrera, Gisella
Gargano, Francesca
Pieri, Massimo
Bernardini, Sergio
Biagio Mercuri, Nicola
Battistini, Luca
Sancesario, Giulia Maria
author_facet Schirinzi, Tommaso
Zenuni, Henri
Grillo, Piergiorgio
Bovenzi, Roberta
Guerrera, Gisella
Gargano, Francesca
Pieri, Massimo
Bernardini, Sergio
Biagio Mercuri, Nicola
Battistini, Luca
Sancesario, Giulia Maria
author_sort Schirinzi, Tommaso
collection PubMed
description Relevance of blood-based biomarkers is increasing into the neurodegenerative diseases field, but data on Parkinson's disease (PD) remain still scarce. In this study, we used the SiMoA technique to measure serum content of total tau protein and amyloid-β peptides (Aβ-42, Aβ-40) in 22 PD patients and ten control subjects. Serum levels of each biomarker were correlated with the respective CSF levels in both the groups; in PD patients, also the correlations between serum biomarkers and main clinical parameters were tested (motor, non-motor, cognitive scores and levodopa equivalent daily dose). Serum biomarkers did not exhibit quantitative differences between patients and controls; however, only PD patients had inter-fluids (serum-CSF) associations in tau and amyloid-β-42 levels. Moreover, serum content of tau protein was inversely correlated with cognitive performances (MoCA score). These findings, albeit preliminary, indicate that brain-derived peptides may change in parallel in both peripheral blood and CSF of PD patients, eventually even in association with some clinical features. Further studies are now needed to validate the use of blood-based biomarkers in PD.
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spelling pubmed-89141012022-03-12 Tau and Amyloid-β Peptides in Serum of Patients With Parkinson's Disease: Correlations With CSF Levels and Clinical Parameters Schirinzi, Tommaso Zenuni, Henri Grillo, Piergiorgio Bovenzi, Roberta Guerrera, Gisella Gargano, Francesca Pieri, Massimo Bernardini, Sergio Biagio Mercuri, Nicola Battistini, Luca Sancesario, Giulia Maria Front Neurol Neurology Relevance of blood-based biomarkers is increasing into the neurodegenerative diseases field, but data on Parkinson's disease (PD) remain still scarce. In this study, we used the SiMoA technique to measure serum content of total tau protein and amyloid-β peptides (Aβ-42, Aβ-40) in 22 PD patients and ten control subjects. Serum levels of each biomarker were correlated with the respective CSF levels in both the groups; in PD patients, also the correlations between serum biomarkers and main clinical parameters were tested (motor, non-motor, cognitive scores and levodopa equivalent daily dose). Serum biomarkers did not exhibit quantitative differences between patients and controls; however, only PD patients had inter-fluids (serum-CSF) associations in tau and amyloid-β-42 levels. Moreover, serum content of tau protein was inversely correlated with cognitive performances (MoCA score). These findings, albeit preliminary, indicate that brain-derived peptides may change in parallel in both peripheral blood and CSF of PD patients, eventually even in association with some clinical features. Further studies are now needed to validate the use of blood-based biomarkers in PD. Frontiers Media S.A. 2022-02-25 /pmc/articles/PMC8914101/ /pubmed/35280296 http://dx.doi.org/10.3389/fneur.2022.748599 Text en Copyright © 2022 Schirinzi, Zenuni, Grillo, Bovenzi, Guerrera, Gargano, Pieri, Bernardini, Biagio Mercuri, Battistini and Sancesario. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Schirinzi, Tommaso
Zenuni, Henri
Grillo, Piergiorgio
Bovenzi, Roberta
Guerrera, Gisella
Gargano, Francesca
Pieri, Massimo
Bernardini, Sergio
Biagio Mercuri, Nicola
Battistini, Luca
Sancesario, Giulia Maria
Tau and Amyloid-β Peptides in Serum of Patients With Parkinson's Disease: Correlations With CSF Levels and Clinical Parameters
title Tau and Amyloid-β Peptides in Serum of Patients With Parkinson's Disease: Correlations With CSF Levels and Clinical Parameters
title_full Tau and Amyloid-β Peptides in Serum of Patients With Parkinson's Disease: Correlations With CSF Levels and Clinical Parameters
title_fullStr Tau and Amyloid-β Peptides in Serum of Patients With Parkinson's Disease: Correlations With CSF Levels and Clinical Parameters
title_full_unstemmed Tau and Amyloid-β Peptides in Serum of Patients With Parkinson's Disease: Correlations With CSF Levels and Clinical Parameters
title_short Tau and Amyloid-β Peptides in Serum of Patients With Parkinson's Disease: Correlations With CSF Levels and Clinical Parameters
title_sort tau and amyloid-β peptides in serum of patients with parkinson's disease: correlations with csf levels and clinical parameters
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8914101/
https://www.ncbi.nlm.nih.gov/pubmed/35280296
http://dx.doi.org/10.3389/fneur.2022.748599
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