Utility of plasma Neurofilament light as a diagnostic and prognostic biomarker of the postural instability gait disorder motor subtype in early Parkinson's disease.


Journal

Molecular neurodegeneration
ISSN: 1750-1326
Titre abrégé: Mol Neurodegener
Pays: England
ID NLM: 101266600

Informations de publication

Date de publication:
05 06 2020
Historique:
received: 13 01 2020
accepted: 28 05 2020
entrez: 7 6 2020
pubmed: 7 6 2020
medline: 2 7 2021
Statut: epublish

Résumé

The main motor subtypes of Parkinson's disease (PD) include tremor-dominant (TD) and postural instability gait disorder (PIGD), with varying disease course that warrant the development of biomarkers capable of predicting progression according to motor subtype. The PIGD subtype is associated with a poorer prognosis, hence identification of a biomarker associated with PIGD is clinically relevant. Neurofilament light (NfL) chain is a potential biomarker of disease severity in neurological disorders including PD. However, no study has investigated NfL and PD motor subtypes. Here, we aimed to investigate the diagnostic and prognostic utility of plasma NfL for PD motor subtypes in early Parkinson's disease. Given the higher risk for cognitive and motor decline in PIGD, we hypothesized that plasma NfL is a potential biomarker for PIGD. Plasma NfL was measured in 199 participants (149 PD and 50 healthy controls, HC) using an ultrasensitive single molecule array. Patients were classified into TD or PIGD based on MDS-UPDRS components. After 2 years, 115 patients were reassessed. Association between NfL and clinical measures in PIGD and TD at baseline and at 2-year follow-up were analysed. At baseline, plasma NfL levels were higher in PD than HC (8.8 ± 3.4 vs 16.2 ± 7.6 pg/ml, p < 0.0001), and differentiated PD from HC with a good diagnostic accuracy (AUC = 0.833, p < 0.001). At 2 years, NfL was higher in PIGD than TD (18.4 ± 14.5 vs 12.6 ± 4.4 pg/ml, p = 0.039). Within the PIGD group, higher NfL associated significantly with worse global cognition and UPDRS motor scores at baseline, and was able to predict motor and cognitive decline at a mean follow-up duration of 1.9 years, controlled for age, sex and disease duration. In this longitudinal study, we demonstrated for the first time the potential utility of plasma NfL as a diagnostic and prognostic biomarker in PIGD even at early stages of PD. These important novel findings will require further confirmation in larger, longitudinal PD cohorts.

Sections du résumé

BACKGROUND
The main motor subtypes of Parkinson's disease (PD) include tremor-dominant (TD) and postural instability gait disorder (PIGD), with varying disease course that warrant the development of biomarkers capable of predicting progression according to motor subtype. The PIGD subtype is associated with a poorer prognosis, hence identification of a biomarker associated with PIGD is clinically relevant. Neurofilament light (NfL) chain is a potential biomarker of disease severity in neurological disorders including PD. However, no study has investigated NfL and PD motor subtypes. Here, we aimed to investigate the diagnostic and prognostic utility of plasma NfL for PD motor subtypes in early Parkinson's disease. Given the higher risk for cognitive and motor decline in PIGD, we hypothesized that plasma NfL is a potential biomarker for PIGD.
METHODS
Plasma NfL was measured in 199 participants (149 PD and 50 healthy controls, HC) using an ultrasensitive single molecule array. Patients were classified into TD or PIGD based on MDS-UPDRS components. After 2 years, 115 patients were reassessed. Association between NfL and clinical measures in PIGD and TD at baseline and at 2-year follow-up were analysed.
RESULTS
At baseline, plasma NfL levels were higher in PD than HC (8.8 ± 3.4 vs 16.2 ± 7.6 pg/ml, p < 0.0001), and differentiated PD from HC with a good diagnostic accuracy (AUC = 0.833, p < 0.001). At 2 years, NfL was higher in PIGD than TD (18.4 ± 14.5 vs 12.6 ± 4.4 pg/ml, p = 0.039). Within the PIGD group, higher NfL associated significantly with worse global cognition and UPDRS motor scores at baseline, and was able to predict motor and cognitive decline at a mean follow-up duration of 1.9 years, controlled for age, sex and disease duration.
CONCLUSIONS
In this longitudinal study, we demonstrated for the first time the potential utility of plasma NfL as a diagnostic and prognostic biomarker in PIGD even at early stages of PD. These important novel findings will require further confirmation in larger, longitudinal PD cohorts.

Identifiants

pubmed: 32503574
doi: 10.1186/s13024-020-00385-5
pii: 10.1186/s13024-020-00385-5
pmc: PMC7275464
doi:

Substances chimiques

Biomarkers 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

33

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Auteurs

Adeline Su Lyn Ng (ASL)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore. adeline.ng.s.l@singhealth.com.sg.
Neuroscience and Behavioural Disorders Program, Duke-NUS Medical School, 8 College Road, Bukit Merah, 169857, Singapore. adeline.ng.s.l@singhealth.com.sg.

Yi Jayne Tan (YJ)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Alisa Cui Wen Yong (ACW)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Seyed Ehsan Saffari (SE)

Center for Quantitative Medicine, Duke-NUS Medical School, Bukit Merah, Singapore.

Zhonghao Lu (Z)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Ebonne Yulin Ng (EY)

Department of Neurology, National Neuroscience Institute, Singapore General Hospital, 20 College Road, Bukit Merah, 169856, Singapore.

Samuel Yong Ern Ng (SYE)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Nicole Shuang Yu Chia (NSY)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Xinyi Choi (X)

Department of Neurology, National Neuroscience Institute, Singapore General Hospital, 20 College Road, Bukit Merah, 169856, Singapore.

Dede Heng (D)

Department of Neurology, National Neuroscience Institute, Singapore General Hospital, 20 College Road, Bukit Merah, 169856, Singapore.

Shermyn Neo (S)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Zheyu Xu (Z)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Nicole Chwee Har Keong (NCH)

Neuroscience and Behavioural Disorders Program, Duke-NUS Medical School, 8 College Road, Bukit Merah, 169857, Singapore.
Department of Neurosurgery, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Kay Yaw Tay (KY)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Wing Lok Au (WL)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Louis Chew Seng Tan (LCS)

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Bukit Merah, 308433, Singapore.

Eng-King Tan (EK)

Neuroscience and Behavioural Disorders Program, Duke-NUS Medical School, 8 College Road, Bukit Merah, 169857, Singapore.
Department of Neurology, National Neuroscience Institute, Singapore General Hospital, 20 College Road, Bukit Merah, 169856, Singapore.

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