Temporal trajectory of biofluid markers in Parkinson’s disease
Abstract Full dynamics of biofluid biomarkers have been unknown in patients with Parkinson’s disease (PD). Using data from 396 PD patients and 182 controls in the Parkinson's Progression Markers Initiative (PPMI) database, we estimated long-term temporal trajectories of CSF α-synuclein (α-syn),...
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2021-07-01
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doaj-3329831da03a431783222c65d4549c3b2021-07-25T11:23:33ZengNature Publishing GroupScientific Reports2045-23222021-07-0111111210.1038/s41598-021-94345-8Temporal trajectory of biofluid markers in Parkinson’s diseaseMin Seok Baek0Myung Jun Lee1Han-Kyeol Kim2Chul Hyoung Lyoo3Department of Neurology, Wonju Severance Christian Hospital, Yonsei University Wonju College of MedicineDepartment of Neurology, Pusan National University Hospital, Pusan National University School of Medicine and Biomedical Research InstituteDepartment of Neurology, Gangnam Severance Hospital, Yonsei University College of MedicineDepartment of Neurology, Gangnam Severance Hospital, Yonsei University College of MedicineAbstract Full dynamics of biofluid biomarkers have been unknown in patients with Parkinson’s disease (PD). Using data from 396 PD patients and 182 controls in the Parkinson's Progression Markers Initiative (PPMI) database, we estimated long-term temporal trajectories of CSF α-synuclein (α-syn), amyloid-β (Aβ), total tau (t-tau), phosphorylated tau (p-tau) and serum neurofilament light chain (NfL) by integrating function between the baseline levels and annual changes. At baseline, PD patients showed lower CSF α-syn, Aβ, t-tau and p-tau levels than those of the controls. In all PD patients, CSF α-syn and Aβ decreased in a negative exponential pattern before the onset of motor symptoms, whereas CSF t-tau and p-tau, and serum NfL increased. Patients with cognitive impairment exhibited faster decline of Aβ and α-syn and faster rise of t-tau, p-tau and NfL, when compared to those without. Similarly, low Aβ group showed earlier decline of α-syn, faster rise of t-tau, p-tau and NfL, and faster decline of cognitive performances, when compared to high Aβ group. Our results suggest that longitudinal changes in biomarkers can be influenced by cognitive impairment and Aβ burden at baseline. PD patients with Aβ pathology may be associated with early appearance of α-synuclein pathology, rapid progression of axonal degeneration and neurodegeneration, and consequently greater cognitive decline.https://doi.org/10.1038/s41598-021-94345-8 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Min Seok Baek Myung Jun Lee Han-Kyeol Kim Chul Hyoung Lyoo |
spellingShingle |
Min Seok Baek Myung Jun Lee Han-Kyeol Kim Chul Hyoung Lyoo Temporal trajectory of biofluid markers in Parkinson’s disease Scientific Reports |
author_facet |
Min Seok Baek Myung Jun Lee Han-Kyeol Kim Chul Hyoung Lyoo |
author_sort |
Min Seok Baek |
title |
Temporal trajectory of biofluid markers in Parkinson’s disease |
title_short |
Temporal trajectory of biofluid markers in Parkinson’s disease |
title_full |
Temporal trajectory of biofluid markers in Parkinson’s disease |
title_fullStr |
Temporal trajectory of biofluid markers in Parkinson’s disease |
title_full_unstemmed |
Temporal trajectory of biofluid markers in Parkinson’s disease |
title_sort |
temporal trajectory of biofluid markers in parkinson’s disease |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-07-01 |
description |
Abstract Full dynamics of biofluid biomarkers have been unknown in patients with Parkinson’s disease (PD). Using data from 396 PD patients and 182 controls in the Parkinson's Progression Markers Initiative (PPMI) database, we estimated long-term temporal trajectories of CSF α-synuclein (α-syn), amyloid-β (Aβ), total tau (t-tau), phosphorylated tau (p-tau) and serum neurofilament light chain (NfL) by integrating function between the baseline levels and annual changes. At baseline, PD patients showed lower CSF α-syn, Aβ, t-tau and p-tau levels than those of the controls. In all PD patients, CSF α-syn and Aβ decreased in a negative exponential pattern before the onset of motor symptoms, whereas CSF t-tau and p-tau, and serum NfL increased. Patients with cognitive impairment exhibited faster decline of Aβ and α-syn and faster rise of t-tau, p-tau and NfL, when compared to those without. Similarly, low Aβ group showed earlier decline of α-syn, faster rise of t-tau, p-tau and NfL, and faster decline of cognitive performances, when compared to high Aβ group. Our results suggest that longitudinal changes in biomarkers can be influenced by cognitive impairment and Aβ burden at baseline. PD patients with Aβ pathology may be associated with early appearance of α-synuclein pathology, rapid progression of axonal degeneration and neurodegeneration, and consequently greater cognitive decline. |
url |
https://doi.org/10.1038/s41598-021-94345-8 |
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