Batzu, Lucia;
Rota, Silvia;
Hye, Abdul;
Heslegrave, Amanda;
Trivedi, Dhaval;
Gibson, Lucy L;
Farrell, Chloe;
... Aarsland, Dag; + view all
(2022)
Plasma p-tau181, neurofilament light chain and association with cognition in Parkinson's disease.
npj Parkinson's Disease
, 8
, Article 154. 10.1038/s41531-022-00384-x.
Preview |
Text
s41531-022-00384-x.pdf - Published Version Download (826kB) | Preview |
Abstract
Early identification of cognitive impairment in Parkinson’s disease (PD) has important clinical and research implications. The aim of our study was to investigate the role of plasma tau phosphorylated at amino acid 181 (p-tau181) and plasma neurofilament light chain (NfL) as biomarkers of cognition in PD. Baseline concentrations of plasma p-tau181 and NfL were measured in a cohort of 136 patients with PD and 63 healthy controls (HC). Forty-seven PD patients were followed up for up to 2 years. Cross-sectional and longitudinal associations between baseline plasma biomarkers and cognitive progression were investigated using linear regression and linear mixed effects models. At baseline, plasma p-tau181 concentration was significantly higher in PD subjects compared with HC (p = 0.026). In PD patients, higher plasma NfL was associated with lower MMSE score at baseline, after adjusting for age, sex and education (p = 0.027). Baseline plasma NfL also predicted MMSE decline over time in the PD group (p = 0.020). No significant association between plasma p-tau181 concentration and baseline or longitudinal cognitive performance was found. While the role of p-tau181 as a diagnostic biomarker for PD and its relationship with cognition need further elucidation, plasma NfL may serve as a feasible, non-invasive biomarker of cognitive progression in PD.
Type: | Article |
---|---|
Title: | Plasma p-tau181, neurofilament light chain and association with cognition in Parkinson's disease |
Location: | United States |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1038/s41531-022-00384-x |
Publisher version: | https://doi.org/10.1038/s41531-022-00384-x |
Language: | English |
Additional information: | This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
Keywords: | Science & Technology, Life Sciences & Biomedicine, Neurosciences, Neurosciences & Neurology, NONMOTOR SYMPTOMS SCALE, ALZHEIMERS-DISEASE, TAU, BIOMARKER, IMPAIRMENT, PREDICTION, DIAGNOSIS, ACCURACY, DEMENTIA, DECLINE |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases |
URI: | https://discovery.ucl.ac.uk/id/eprint/10162570 |
Archive Staff Only
View Item |