血浆和脑脊液β-突触核蛋白对散发性克雅氏病的高诊断性能

IF 4.4 2区 医学 Q1 CLINICAL NEUROLOGY
Samir Abu-Rumeileh, Steffen Halbgebauer, Giuseppe Mario Bentivenga, Lorenzo Barba, Simone Baiardi, Andrea Mastrangelo, Patrick Oeckl, Petra Steinacker, Angela Mammana, Sabina Capellari, Markus Otto, Piero Parchi
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引用次数: 0

摘要

β-突触核蛋白是一种很有前途的突触损伤的脑脊液和血液生物标志物。在这里,我们分析了它在区分散发性克雅氏病(n = 150)和非朊病毒快速进展性痴呆(n = 106)。在脑脊液中,β-突触核蛋白的表现优于蛋白质14-3-3(AUC 0.95 vs.0.89),在较小程度上优于总τ(AUC 0.92)。此外,血浆β-突触蛋白(AUC 0.9 1)的诊断价值优于血浆τ(AUC0.79)和神经丝轻链蛋白(AUC0.65),与脑脊液生物标志物的诊断价值相当。β-突触核蛋白可能是诊断散发性克雅氏病的第一个高度准确的血液生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High diagnostic performance of plasma and cerebrospinal fluid beta-synuclein for sporadic Creutzfeldt–Jakob disease

High diagnostic performance of plasma and cerebrospinal fluid beta-synuclein for sporadic Creutzfeldt–Jakob disease

Beta-synuclein is a promising cerebrospinal fluid and blood biomarker of synaptic damage. Here we analysed its accuracy in the discrimination between sporadic Creutzfeldt–Jakob disease (n = 150) and non-prion rapidly progressive dementias (n = 106). In cerebrospinal fluid, beta-synuclein performed better than protein 14-3-3 (AUC 0.95 vs. 0.89) and, to a lesser extent, than total tau (AUC 0.92). Further, the diagnostic value of plasma beta-synuclein (AUC 0.91) outperformed that of plasma tau (AUC 0.79) and neurofilament light chain protein (AUC 0.65) and was comparable to that of cerebrospinal fluid biomarkers. Beta-synuclein might represent the first highly accurate blood biomarker for the diagnosis of sporadic Creutzfeldt–Jakob disease.

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来源期刊
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology Medicine-Neurology (clinical)
CiteScore
9.10
自引率
1.90%
发文量
218
审稿时长
8 weeks
期刊介绍: Annals of Clinical and Translational Neurology is a peer-reviewed journal for rapid dissemination of high-quality research related to all areas of neurology. The journal publishes original research and scholarly reviews focused on the mechanisms and treatments of diseases of the nervous system; high-impact topics in neurologic education; and other topics of interest to the clinical neuroscience community.
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