使用深度学习方法评估多种神经退行性蛋白对克雅氏病诊断的敏感性和特异性

IF 1.9 3区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Prion Pub Date : 2019-01-01 DOI:10.1080/19336896.2019.1639482
Sol Moe Lee, Jae Wook Hyeon, Soo-Jin Kim, Heebal Kim, Ran Noh, Seonghan Kim, Yeong Seon Lee, Su Yeon Kim
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引用次数: 3

摘要

散发性克雅氏病(sCJD)的诊断只能通过死后脑组织中蛋白酶抗性朊蛋白的异常积累来证实。sCJD与脑脊液蛋白(CSF)之间的关系,如14-3-3,tau和α-突触核蛋白(a-syn),已被研究其在死前诊断中的潜在价值。近年来,深度学习方法在神经退行性疾病的研究中受到了广泛的关注。我们建立了使用多种脑脊液生物标志物的dl辅助克雅氏病死前诊断方法,以提高其区分敏感性和特异性。采用酶联免疫吸附法检测磷酸化tau蛋白(p-tau)、总tau蛋白(t-tau)、a-syn蛋白和β-淀粉样蛋白(1-42),并对49例sCJD和256例非cjd韩国患者脑脊液样本中的14-3-3蛋白进行western blot分析。深度神经网络结构由1个输入层、5个隐藏层和1个输出层组成,每个隐藏层分别有20、40、30、20和12个隐藏单元号。表现最好的DL模型对t-tau、p-tau和a-syn三种蛋白组合的准确性为90.38%,敏感性为83.33%,特异性为92.5%,而在单独的CSF组中(n = 15)患有其他神经元疾病的所有其他患者都能正确预测没有CJD。因此,dl辅助的死前诊断可能为区分CJD患者和非CJD患者提供一种合适的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Sensitivity and specificity evaluation of multiple neurodegenerative proteins for Creutzfeldt-Jakob disease diagnosis using a deep-learning approach.

The diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD) can only be confirmed by abnormal protease-resistant prion protein accumulation in post-mortem brain tissue. The relationships between sCJD and cerebrospinal fluid (CSF) proteins such as 14-3-3, tau, and α-synuclein (a-syn) have been investigated for their potential value in pre-mortem diagnosis. Recently, deep-learning (DL) methods have attracted attention in neurodegenerative disease research. We established DL-aided pre-mortem diagnostic methods for CJD using multiple CSF biomarkers to improve their discriminatory sensitivity and specificity. Enzyme-linked immunosorbent assays were performed on phospho-tau (p-tau), total-tau (t-tau), a-syn, and β-amyloid (1-42), and western blot analysis was performed for 14-3-3 protein from CSF samples of 49 sCJD and 256 non-CJD Korean patients, respectively. The deep neural network structure comprised one input, five hidden, and one output layers, with 20, 40, 30, 20 and 12 hidden unit numbers per hidden layer, respectively. The best performing DL model demonstrated 90.38% accuracy, 83.33% sensitivity, and 92.5% specificity for the three-protein combination of t-tau, p-tau, and a-syn, and all other patients in a separate CSF set (n = 15) with other neuronal diseases were correctly predicted to not have CJD. Thus, DL-aided pre-mortem diagnosis may provide a suitable tool for discriminating CJD patients from non-CJD patients.

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来源期刊
Prion
Prion 生物-生化与分子生物学
CiteScore
5.20
自引率
4.30%
发文量
13
审稿时长
6-12 weeks
期刊介绍: Prion is the first international peer-reviewed open access journal to focus exclusively on protein folding and misfolding, protein assembly disorders, protein-based and structural inheritance. The goal is to foster communication and rapid exchange of information through timely publication of important results using traditional as well as electronic formats. The overriding criteria for publication in Prion are originality, scientific merit and general interest.
期刊最新文献
A case report of fatal familial insomnia with cerebrospinal fluid leukocytosis during the COVID-19 epidemic and review of the literature. A systemic analysis of Creutzfeldt Jakob disease cases in Asia. Mutations in human prion-like domains: pathogenic but not always amyloidogenic. Prion forensics: a multidisciplinary approach to investigate CWD at an illegal deer carcass disposal site. Exploring CJD incidence trends: insights from Slovakia.
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