Cerebrospinal Fluid Total and Phosphorylated α-Synuclein in Patients with Creutzfeldt-Jakob Disease and Synucleinopathy.

Cerebrospinal fluid Creutzfeldt–Jakob disease Dementia with Lewy bodies Parkinson’s disease Phospho-serine-129 α-synuclein T-α-synuclein

Journal

Molecular neurobiology
ISSN: 1559-1182
Titre abrégé: Mol Neurobiol
Pays: United States
ID NLM: 8900963

Informations de publication

Date de publication:
May 2019
Historique:
received: 15 05 2018
accepted: 09 08 2018
pubmed: 24 8 2018
medline: 14 8 2019
entrez: 24 8 2018
Statut: ppublish

Résumé

High levels of total α-synuclein (t-α-synuclein) in the cerebrospinal fluid (CSF) were reported in sporadic Creutzfeldt-Jakob disease (sCJD). The potential use of t-α-synuclein in the discrimination of Lewy body dementias (i.e., Parkinson's disease dementia (PDD) and dementia with Lewy bodies (DLB)) is still under investigation. In addition, phospho-serine-129 α-synuclein (p-α-synuclein) has been described to be slightly increased in the CSF of synucleinopathies. Here, we analyzed t-α-synuclein and p-α-synuclein concentrations and their ratio in the context of differential diagnosis of neurodegenerative diseases. We quantified the levels of CSF t-α-synuclein and p-α-synuclein in a cohort of samples composed of neurological controls (NC), sCJD, PDD, and DLB by means of newly developed specific enzyme-linked immunosorbent assays. T-α-synuclein and p-α-synuclein were specifically elevated in sCJD compared to other disease groups. The area under the curve (AUC) values for t-α-synuclein were higher for the discrimination of sCJD from dementias associated to Lewy bodies as compared to the use of p-α-synuclein. A combination of both markers even increased the diagnostic accuracy. An inverse correlation was observed in CSF between t-α-synuclein and p-α-synuclein, especially in the DLB group, indicating a disease-relevant association between both markers. In conclusion, our data confirm t-α-synuclein and p-α-synuclein as robust biomarkers for sCJD and indicate the potential use of colorimetric t-α-synuclein ELISAs for differential diagnosis of dementia types.

Identifiants

pubmed: 30136097
doi: 10.1007/s12035-018-1313-4
pii: 10.1007/s12035-018-1313-4
doi:

Substances chimiques

Phosphoproteins 0
alpha-Synuclein 0

Types de publication

Journal Article

Langues

eng

Pagination

3476-3483

Subventions

Organisme : Spanish Ministry of Health
ID : CP16/00041
Organisme : Michael J. Fox Foundation for Parkinson's Research
ID : 10147
Organisme : NIA Grant
ID : AG-10124

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Auteurs

Matthias Schmitz (M)

Department of Neurology, University Medical Center Goettingen, Goettingen, Germany. matthias.schmitz@med.uni-goettingen.de.

Anna Villar-Piqué (A)

Department of Neurology, University Medical Center Goettingen, Goettingen, Germany. annavillarpique@gmail.com.

Franc Llorens (F)

Department of Neurology, University Medical Center Goettingen, Goettingen, Germany. franc.llorens@gmail.com.
Network Center for Biomedical Research in Neurodegenerative Diseases (CIBERNED), Barcelona, Spain. franc.llorens@gmail.com.
Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain. franc.llorens@gmail.com.

Karin Gmitterová (K)

Second Department of Neurology, Comenius University, Bratislava, Slovakia.
Department of Neurology, University Medical Center Goettingen, Goettingen, Germany.

Peter Hermann (P)

Department of Neurology, University Medical Center Goettingen, Goettingen, Germany.

Daniela Varges (D)

Department of Neurology, University Medical Center Goettingen, Goettingen, Germany.

Saima Zafar (S)

Department of Neurology, University Medical Center Goettingen, Goettingen, Germany.

Paul Lingor (P)

Department of Neurology, University Medical Center Goettingen, Goettingen, Germany.

Hugo Vanderstichele (H)

ADx NeuroSciences, Technologiepark 4, Ghent, Belgium.

Leentje Demeyer (L)

ADx NeuroSciences, Technologiepark 4, Ghent, Belgium.

Erik Stoops (E)

ADx NeuroSciences, Technologiepark 4, Ghent, Belgium.

John Q Trojanowski (JQ)

Center for Neurodegenerative Research and Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.

Virginia M-Y Lee (VM)

Center for Neurodegenerative Research and Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.

Inga Zerr (I)

Department of Neurology, University Medical Center Goettingen, Goettingen, Germany.

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