Increased alpha-synuclein tear fluid levels in patients with Parkinson’s disease

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作者
Fabian Maass
Sebastian Rikker
Vivian Dambeck
Carmina Warth
Lars Tatenhorst
Ilona Csoti
Matthias Schmitz
Inga Zerr
Andreas Leha
Mathias Bähr
Paul Lingor
机构
[1] Department of Neurology,
[2] University Medical Center,undefined
[3] Gertrudis Clinic Parkinson-Center,undefined
[4] DZNE,undefined
[5] German Center for Neurodegenerative Diseases,undefined
[6] Department of Medical Statistics,undefined
[7] University Medical Center,undefined
[8] Cluster of Excellence Nanoscale Microscopy and Molecular Physiology of the Brain (CNMPB),undefined
[9] Center for Biostructural Imaging of Neurodegeneration (BIN),undefined
[10] University Medical Center,undefined
[11] Technical University of Munich,undefined
[12] School of Medicine,undefined
[13] Klinikum rechts der Isar,undefined
[14] Department of Neurology,undefined
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摘要
The objective of the study was to estimate if altered levels of alpha-synuclein can be detected in tear fluid of patients with Parkinson’s disease (PD). Therefore, tear fluid samples of 75 PD patients, 75 control subjects and 31 atypical Parkinsonian patients were collected and analyzed in triplicates using an ultra-sensitive single molecule array (SIMOA) system and applying a human alpha-synuclein immunoassay. In PD, levels of total soluble alpha-synuclein were significantly increased compared to control subjects (p = 0.03; AUC PD vs. controls 0.60). There was no difference comparing PD patients stratified by Hoehn & Yahr stages and atypical Parkinsonian syndromes stratified by tauopathies and non-PD-synucleinopathies against each other (p > 0.05). In conclusion, alpha-synuclein can be detected and quantified in tear fluid, revealing small but significant differences in total alpha-synuclein levels between PD and control subjects. Tear fluid can be collected non-invasively and risk-free, therefore presenting a promising source for further biomarker research.
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