Phosphorylated α-Synuclein in Parkinson’s Disease

Yu Wang(University of Washington), Min Shi(University of Washington), Kathryn A. Chung(Oregon Health & Science University), Cyrus P. Zabetian(University of Puget Sound), James B. Leverenz(University of Washington), Daniela Berg(German Center for Neurodegenerative Diseases), Karin Srulijes(German Center for Neurodegenerative Diseases), John Q. Trojanowski(Institute for Neurodegenerative Disorders), Virginia M.‐Y. Lee(Institute for Neurodegenerative Disorders), Andrew Siderowf(University of Pennsylvania), Howard I. Hurtig(University of Pennsylvania), Irene Litvan(University of Louisville), Mya C. Schiess(The University of Texas Health Science Center at Houston), Elaine R. Peskind(University of Washington), M. Masuda(Tokyo Metropolitan Institute of Medical Science), Masato Hasegawa(Tokyo Metropolitan Institute of Medical Science), Xiangmin Lin(University of Washington), Catherine Pan(University of Washington), Douglas Galasko(University of California San Diego), David S. Goldstein(National Institute of Neurological Disorders and Stroke), Poul Henning Jensen(Aarhus University), Hui Yang(University of Washington), Kevin C. Cain(University of Washington), Jing Zhang(University of Washington)
Science Translational Medicine
February 15, 2012
Cited by 275Open Access
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Abstract

Phosphorylated α-synuclein (PS-129), a protein implicated in the pathogenesis of Parkinson's disease (PD), was identified by mass spectrometry in human cerebrospinal fluid (CSF). A highly sensitive and specific assay was established and used to measure PS-129 together with total α-synuclein in the CSF of patients with PD, other parkinsonian disorders such as multiple system atrophy (MSA) and progressive supranuclear palsy (PSP), and healthy individuals (a total of ~600 samples). PS-129 CSF concentrations correlated weakly with PD severity and, when combined with total α-synuclein concentrations in CSF, contributed to distinguishing PD from MSA and PSP. Further rigorous validation in independent cohorts of patients, especially those where samples have been collected longitudinally, will determine whether the concentration of PS-129 in CSF will be useful for diagnosing PD and for monitoring PD severity and progression.


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