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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Published in | Frontiers in neurology Vol. 13; p. 748599 |
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Main Authors | , , , , , , , , , , |
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Abstract | 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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AbstractList | 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. 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.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. |
Author | Grillo, Piergiorgio Pieri, Massimo Bernardini, Sergio Zenuni, Henri Guerrera, Gisella Gargano, Francesca Biagio Mercuri, Nicola Bovenzi, Roberta Schirinzi, Tommaso Sancesario, Giulia Maria Battistini, Luca |
AuthorAffiliation | 2 European Centre for Brain Research, IRCCS Fondazione Santa Lucia , Rome , Italy 1 Unit of Neurology, Department of Systems Medicine, University of Roma Tor Vergata , Rome , Italy 3 Department of Experimental Medicine, University of Roma Tor Vergata , Rome , Italy |
AuthorAffiliation_xml | – name: 2 European Centre for Brain Research, IRCCS Fondazione Santa Lucia , Rome , Italy – name: 3 Department of Experimental Medicine, University of Roma Tor Vergata , Rome , Italy – name: 1 Unit of Neurology, Department of Systems Medicine, University of Roma Tor Vergata , Rome , Italy |
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Copyright | Copyright © 2022 Schirinzi, Zenuni, Grillo, Bovenzi, Guerrera, Gargano, Pieri, Bernardini, Biagio Mercuri, Battistini and Sancesario. Copyright © 2022 Schirinzi, Zenuni, Grillo, Bovenzi, Guerrera, Gargano, Pieri, Bernardini, Biagio Mercuri, Battistini and Sancesario. 2022 Schirinzi, Zenuni, Grillo, Bovenzi, Guerrera, Gargano, Pieri, Bernardini, Biagio Mercuri, Battistini and Sancesario |
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Keywords | tau Parkinson's disease blood biomarkers SiMoA fluid biomarkers CSF biomarkers |
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License | Copyright © 2022 Schirinzi, Zenuni, Grillo, Bovenzi, Guerrera, Gargano, Pieri, Bernardini, Biagio Mercuri, Battistini and Sancesario. 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. |
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References | Qiu (B19) 2015; 21 Sancesario (B7) 2017; 55 Janelidze (B18) 2016; 6 Pan (B21) 2021; 71 Palmqvist (B8) 2021; 27 Schirinzi (B2) 2019; 61 Shi (B15) 2014; 128 Lang (B1) 2018; 33 Teunissen (B6) 2018; 10 Schirinzi (B16) 2017; 124 Abbasi (B22) 2018; 33 Schirinzi (B11) 2015; 6 Fossati (B17) 2019; 11 Zhang (B23) 2016; 11 Petrillo (B3) 2020; 35 Ashton (B14) 2020; 16 Roeben (B20) 2016; 52 Zenuni (B13) 2021; 5 Schirinzi (B9) 2020; 90 Schirinzi (B10) 2021 Parnetti (B4) 2019; 18 Sancesario (B5) 2015; 52 Sancesario (B12) 2020; 76 |
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Title | Tau and Amyloid-β Peptides in Serum of Patients With Parkinson's Disease: Correlations With CSF Levels and Clinical Parameters |
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