TY - JOUR
T1 - Cerebrospinal fluid biomarkers in Parkinson disease
AU - Parnetti, Lucilla
AU - Castrioto, Anna
AU - Chiasserini, Davide
AU - Persichetti, Emanuele
AU - Tambasco, Nicola
AU - El-Agnaf, Omar
AU - Calabresi, Paolo
N1 - Funding Information:
P. Calabresi receives grant support from Ricerca Corrente IRCCS and Ricerca Finalizzata IRCCS (European Community Grant REPLACES). O. El‑Agnaf and L. Parnetti have been supported by, and E. Persichetti receives a salary from, the Michael J. Fox Foundation for Parkinson’s Disease. D. Chiasserini is supported by the European 7th framework project MEFOPA (Mendelian Forms of Parkinson’s disease; EU grant 241791).
PY - 2013/3
Y1 - 2013/3
N2 - Clinical diagnosis of Parkinson disease (PD) is difficult in early stages of disease, with high risk of misdiagnosis. The long preclinical phase of PD provides the possibility for early therapeutic intervention once disease-modifying therapies have been developed, but lack of biomarkers for early diagnosis and monitoring of disease progression represents a major obstacle to achievement of this goal. Accordingly, research efforts aimed at identification of novel biomarkers have been increasing in the past 5 years. Cerebrospinal fluid (CSF) is an accessible source of brain-derived proteins, which mirror molecular changes that take place in the CNS. In this Review, we discuss evidence from numerous studies that have focused on identification of candidate CSF biomarkers for PD. Notably, molecular pathways related to α-synuclein, tau and β-amyloid peptides have received considerable attention. CSF levels of the protein DJ-1 are also of interest, although further investigation of this candidate marker is required. These studies support the usefulness of a combination of various CSF biomarkers of PD to increase diagnostic accuracy during early phases of the disease, and to differentiate PD from other neurodegenerative disorders.
AB - Clinical diagnosis of Parkinson disease (PD) is difficult in early stages of disease, with high risk of misdiagnosis. The long preclinical phase of PD provides the possibility for early therapeutic intervention once disease-modifying therapies have been developed, but lack of biomarkers for early diagnosis and monitoring of disease progression represents a major obstacle to achievement of this goal. Accordingly, research efforts aimed at identification of novel biomarkers have been increasing in the past 5 years. Cerebrospinal fluid (CSF) is an accessible source of brain-derived proteins, which mirror molecular changes that take place in the CNS. In this Review, we discuss evidence from numerous studies that have focused on identification of candidate CSF biomarkers for PD. Notably, molecular pathways related to α-synuclein, tau and β-amyloid peptides have received considerable attention. CSF levels of the protein DJ-1 are also of interest, although further investigation of this candidate marker is required. These studies support the usefulness of a combination of various CSF biomarkers of PD to increase diagnostic accuracy during early phases of the disease, and to differentiate PD from other neurodegenerative disorders.
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U2 - 10.1038/nrneurol.2013.10
DO - 10.1038/nrneurol.2013.10
M3 - Review article
C2 - 23419373
AN - SCOPUS:84874948898
SN - 1759-4758
VL - 9
SP - 131
EP - 140
JO - Nature Reviews Neurology
JF - Nature Reviews Neurology
IS - 3
ER -