Plasma Neurofilament Light Concentration Is Associated with Diffusion-Tensor MRI-Based Measures of Neurodegeneration in Early Parkinson's Disease.


Journal

Journal of Parkinson's disease
ISSN: 1877-718X
Titre abrégé: J Parkinsons Dis
Pays: Netherlands
ID NLM: 101567362

Informations de publication

Date de publication:
2022
Historique:
pubmed: 5 9 2022
medline: 19 10 2022
entrez: 4 9 2022
Statut: ppublish

Résumé

Neurofilament light is a marker of axonal degeneration, whose measurement from peripheral blood was recently made possible by new assays. We aimed to determine whether plasma neurofilament light chain (NfL) concentration reflects brain white matter integrity in patients with early Parkinson's disease (PD). 137 early PD patients and 51 healthy controls were included. Plasma NfL levels were measured using ultrasensitive single molecule array. 3T MRI including diffusion tensor imaging was acquired for voxelwise analysis of association between NfL and both fractional anisotropy (FA) and mean diffusivity (MD) in white matter tracts and subcortical nuclei. A pattern of brain microstructural changes consistent with neurodegeneration was associated with increased plasma NfL in most of the frontal lobe and right internal capsule, with decreased FA and increased MD. The same clusters were also associated with poorer global cognition. A significant cluster in the left putamen was associated with increased NfL, with a significantly greater effect in PD than controls. Plasma NfL may be associated with brain microstructure, as measured using diffusion tensor imaging, in patients with early PD. Higher plasma NfL was associated with a frontal pattern of neurodegeneration that also correlates with cognitive performance in our cohort. This may support a future role for plasma NfL as an accessible biomarker for neurodegeneration and cognitive dysfunction in PD.

Sections du résumé

BACKGROUND
Neurofilament light is a marker of axonal degeneration, whose measurement from peripheral blood was recently made possible by new assays.
OBJECTIVE
We aimed to determine whether plasma neurofilament light chain (NfL) concentration reflects brain white matter integrity in patients with early Parkinson's disease (PD).
METHODS
137 early PD patients and 51 healthy controls were included. Plasma NfL levels were measured using ultrasensitive single molecule array. 3T MRI including diffusion tensor imaging was acquired for voxelwise analysis of association between NfL and both fractional anisotropy (FA) and mean diffusivity (MD) in white matter tracts and subcortical nuclei.
RESULTS
A pattern of brain microstructural changes consistent with neurodegeneration was associated with increased plasma NfL in most of the frontal lobe and right internal capsule, with decreased FA and increased MD. The same clusters were also associated with poorer global cognition. A significant cluster in the left putamen was associated with increased NfL, with a significantly greater effect in PD than controls.
CONCLUSION
Plasma NfL may be associated with brain microstructure, as measured using diffusion tensor imaging, in patients with early PD. Higher plasma NfL was associated with a frontal pattern of neurodegeneration that also correlates with cognitive performance in our cohort. This may support a future role for plasma NfL as an accessible biomarker for neurodegeneration and cognitive dysfunction in PD.

Identifiants

pubmed: 36057833
pii: JPD223414
doi: 10.3233/JPD-223414
doi:

Substances chimiques

Biomarkers 0
Neurofilament Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2135-2146

Auteurs

Thomas Welton (T)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Neuroscience Academic Clinical Program, Duke-NUS Medical School, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.

Yi Jayne Tan (YJ)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.

Seyed Ehsan Saffari (SE)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.
Centre for Quantitative Medicine, Duke-NUS Medical School, Singapore.

Samuel Y E Ng (SYE)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.

Nicole S Y Chia (NSY)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.

Alisa C W Yong (ACW)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.

Xinyi Choi (X)

Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.
Department of Neurology, National Neuroscience Institute, Singapore General Hospital, Singapore.

Dede Liana Heng (DL)

Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.
Department of Neurology, National Neuroscience Institute, Singapore General Hospital, Singapore.

Yao-Chia Shih (YC)

Radiological Sciences Academic Clinical Program, Duke-NUS Medical School, Singapore.
Graduate Institute of Medicine, Yuan Ze University, Taoyuan City, Taiwan.

Septian Hartono (S)

Neuroscience Academic Clinical Program, Duke-NUS Medical School, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.
Department of Neurology, National Neuroscience Institute, Singapore General Hospital, Singapore.

Weiling Lee (W)

Department of Diagnostic Radiology, Singapore General Hospital, Singapore.

Zheyu Xu (Z)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.

Kay Yaw Tay (KY)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.

Wing Lok Au (WL)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.

Eng-King Tan (EK)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.
Department of Neurology, National Neuroscience Institute, Singapore General Hospital, Singapore.

Ling Ling Chan (LL)

Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.
Radiological Sciences Academic Clinical Program, Duke-NUS Medical School, Singapore.
Department of Diagnostic Radiology, Singapore General Hospital, Singapore.
Neuroscience and Behavioural Disorders Program, Duke-NUS Medical School, Singapore.

Adeline S L Ng (ASL)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.
Neuroscience and Behavioural Disorders Program, Duke-NUS Medical School, Singapore.

Louis C S Tan (LCS)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Parkinson Disease and Movement Disorders Centre, Parkinson Foundation Center of Excellence, National Neuroscience Institute, Singapore, Tan Tock Seng Hospital, Singapore.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH