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Rapid and ultra-sensitive quantitation of disease-associated α-synuclein seeds in brain and cerebrospinal fluid by αSyn RT-QuIC

机译:αSynRT-QuIC快速超灵敏定量脑和脑脊液中与疾病相关的α-突触核蛋白种子

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摘要

The diagnosis and treatment of synucleinopathies such as Parkinson disease and dementia with Lewy bodies would be aided by the availability of assays for the pathogenic disease-associated forms of α-synuclein (αSynD) that are sufficiently sensitive, specific, and practical for analysis of accessible diagnostic specimens. Two recent αSynD seed amplification tests have provided the first prototypes for ultrasensitive and specific detection of αSynD in patients’ cerebrospinal fluid. These prototypic assays require 5–13 days to perform. Here, we describe an improved α-synuclein real time quaking-induced conversion (αSyn RT-QuIC) assay that has similar sensitivity and specificity to the prior assays, but can be performed in 1–2 days with quantitation. Blinded analysis of cerebrospinal fluid from 29 synucleinopathy cases [12 Parkinson’s and 17 dementia with Lewy bodies] and 31 non-synucleinopathy controls, including 16 Alzheimer’s cases, yielded 93% diagnostic sensitivity and 100% specificity for this test so far. End-point dilution analyses allowed quantitation of relative amounts of αSynD seeding activity in cerebrospinal fluid samples, and detection in as little as 0.2 μL. These results confirm that αSynD seeding activity is present in cerebrospinal fluid. We also demonstrate that it can be rapidly detected, and quantitated, even in early symptomatic stages of synucleinopathy.Electronic supplementary materialThe online version of this article (10.1186/s40478-018-0508-2) contains supplementary material, which is available to authorized users.
机译:对路易氏体的帕金森病和痴呆等突触核蛋白病的诊断和治疗,将可以通过足够敏感的与病原性疾病相关的α-突触核蛋白(αSyn D )形式的检测方法得到帮助,具体且实用的分析可及性诊断标本。最近的两项αSyn D 种子扩增试验提供了第一个原型,用于超灵敏,特异性地检测患者脑脊液中的αSyn D 。这些原型检测需要5到13天才能完成。在这里,我们描述了一种改进的α-突触核蛋白实时地震诱导转化(αSynRT-QuIC)测定法,其灵敏度和特异性与以前的测定法相似,但可在1-2天内进行定量分析。迄今为止,对29例突触核蛋白病病例[12例帕金森氏病和17例路易氏体痴呆症]和31例非突触核蛋白病对照(包括16例阿尔茨海默氏病)进行了脑脊液盲法分析,得出该测试的诊断敏感性和特异性为93%。终点稀释分析可定量测定脑脊液样品中αSyn D 接种活性的相对量,并以低至0.2μL的浓度进行检测。这些结果证实在脑脊液中存在αSyn D 接种活性。我们还证明,即使在突触核蛋白病的症状早期阶段,也可以对其进行快速检测和定量。电子补充材料本文的在线版本(10.1186 / s40478-018-0508-2)包含补充材料,可供授权用户使用。

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