Kinetic parameters of alpha-synuclein seed amplification assay correlate with cognitive impairment in patients with Lewy body disorders

被引:0
作者
Stefan Bräuer
Marcello Rossi
Johann Sajapin
Thomas Henle
Thomas Gasser
Piero Parchi
Kathrin Brockmann
Björn H. Falkenburger
机构
[1] University Hospital Carl Gustav Carus,Department of Neurology
[2] Technische Universität Dresden,Department of Food Chemistry
[3] German Center for Neurodegenerative Diseases (DZNE),Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research
[4] IRCCS Istituto delle Scienze Neurologiche di Bologna (ISNB),Department of Biomedical and Neuromotor Sciences
[5] TU Dresden,undefined
[6] Eberhard Karls University Tübingen,undefined
[7] German Center for Neurodegenerative Diseases (DZNE),undefined
[8] University of Bologna,undefined
来源
Acta Neuropathologica Communications | / 11卷
关键词
Alpha-synuclein; Dementia with Lewy bodies; Parkinson’s disease; RT-QuIC; Seed amplification assay;
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摘要
The alpha-synuclein (aSyn) seed amplification assay (SAA) can identify aSyn aggregates as indicator for Lewy body pathology in biomaterials of living patients and help in diagnosing Parkinson´s disease and dementia syndromes. Our objective was to confirm that qualitative results of aSyn SAA are reproducible across laboratories and to determine whether quantitative findings correlate with patient clinical characteristics. Therefore cerebrospinal fluid samples were re-analysed by aSyn SAA in a second laboratory with four technical replicates for each sample. Kinetic parameters derived from each aggregation curve were summarized and correlated with patient characteristics. We found that qualitative findings were identical between the two laboratories for 54 of 55 patient samples. The number of positive replicates for each sample also showed good agreement between laboratories. Moreover, specific kinetic parameters of the SAA showed a strong correlation with clinical parameters, notably with cognitive performance evaluated by the Montreal Cognitive Assessment. We concluded that SAA findings are highly reproducible across laboratories following the same protocol. SAA reports not only the presence of Lewy pathology but is also associated with clinical characteristics. Thus, aSyn SAA can potentially be used for patient stratification and determining the target engagement of aSyn targeting treatments.
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[1]  
Postuma RB(2015)MDS clinical diagnostic criteria for Parkinson’s disease Mov Disord 30 1591-1601
[2]  
Berg D(2018)Importance of low diagnostic accuracy for early Parkinson’s disease Mov Disord 33 1551-1554
[3]  
Stern M(2017)Biomarker-driven phenotyping in Parkinson’s disease: A translational missing link in disease-modifying clinical trials Mov Disord 32 319-324
[4]  
Poewe W(2008)Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking Nat Methods 5 211-212
[5]  
Olanow CW(2021)RT-QuIC detection of pathological α-synuclein in skin punches of patients with Lewy body disease Mov Disord 36 2173-2177
[6]  
Oertel W(2020)α-Synuclein real-time quaking-induced conversion in the submandibular glands of Parkinson’s disease patients Mov Disord 35 268-278
[7]  
Beach TG(2019)Efficient RT-QuIC seeding activity for α-synuclein in olfactory mucosa samples of patients with Parkinson’s disease and multiple system atrophy Transl Neurodegener 8 24-818
[8]  
Adler CH(2016)Alpha-synuclein RT-QuIC in the CSF of patients with alpha-synucleinopathies Ann Clin Transl Neurol 3 812-277
[9]  
Espay AJ(2020)Discriminating α-synuclein strains in Parkinson’s disease and multiple system atrophy Nature 578 273-1455
[10]  
Schwarzschild MA(2018)Rapid and ultra-sensitive quantitation of disease-associated α-synuclein seeds in brain and cerebrospinal fluid by αSyn RT-QuIC Acta Neuropathol Commun 6 7-3071