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1
Characteristics of Korean patients with suspected Creutzfeldt-Jakob disease with 14-3-3 protein in cerebrospinal fluid: Preliminary study of the Korean Creutzfeldt-Jakob disease active surveillance program.脑脊液中14-3-3蛋白阳性的疑似克雅氏病韩国患者的特征:韩国克雅氏病主动监测项目的初步研究
Prion. 2015;9(2):136-43. doi: 10.1080/19336896.2015.1022020.
2
Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.1997-2008 年阿根廷克雅氏病监测。
Neuroepidemiology. 2011;37(3-4):193-202. doi: 10.1159/000331907. Epub 2011 Nov 5.
3
Association of cerebrospinal fluid prion protein levels and the distinction between Alzheimer disease and Creutzfeldt-Jakob disease.脑脊液朊蛋白水平与阿尔茨海默病和克雅氏病的鉴别诊断相关。
JAMA Neurol. 2015 Mar;72(3):267-75. doi: 10.1001/jamaneurol.2014.4068.
4
Surveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007.2006年至2007年中国克雅氏病监测
BMC Public Health. 2008 Oct 18;8:360. doi: 10.1186/1471-2458-8-360.
5
Cerebrospinal Fluid Levels of 14-3-3 Gamma: What Does It Tell Us About Sporadic Creutzfeldt-Jakob Disease?脑脊液中 14-3-3γ蛋白水平:对散发性克雅氏病有何提示?
Pharmacology. 2017;100(5-6):243-245. doi: 10.1159/000479115. Epub 2017 Jul 26.
6
Creutzfeldt–Jakob disease surveillance in Australia: update to December 2017.澳大利亚克雅氏病监测:截至2017年12月的最新情况
Commun Dis Intell (2018). 2019 Jul 16;43. doi: 10.33321/cdi.2019.43.32.
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Cerebrospinal Fluid Biomarkers in the Diagnosis of Creutzfeldt-Jakob Disease in Slovak Patients: over 10-Year Period Review.脑脊液生物标志物在斯洛伐克患者克雅氏病诊断中的应用:10 年回顾性研究。
Mol Neurobiol. 2017 Oct;54(8):5919-5927. doi: 10.1007/s12035-016-0128-4. Epub 2016 Sep 24.
8
[Analyses of 14-3-3 protein in the cerebrospinal fluid in Creutzfeldt-Jakob disease. Preliminary report].[克雅氏病脑脊液中14-3-3蛋白的分析。初步报告]
Neurol Neurochir Pol. 2005 Sep-Oct;39(5):358-65.
9
[Study on the characteristic of Surveillance Creutzfeldt-Jakob disease patients from January to August in 2006 in China].[2006年1月至8月中国克雅氏病监测病例特征研究]
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2007 Sep;21(3):205-7.
10
Creutzfeldt-Jakob disease surveillance in Australia: update to 31 December 2018.澳大利亚克雅氏病监测:截至2018年12月31日的最新情况
Commun Dis Intell (2018). 2019 Aug 15;43. doi: 10.33321/cdi.2019.43.35.

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The importance of ongoing international surveillance for Creutzfeldt-Jakob disease.不断进行克雅氏病国际监测的重要性。
Nat Rev Neurol. 2021 Jun;17(6):362-379. doi: 10.1038/s41582-021-00488-7. Epub 2021 May 10.
2
Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 104 Cases.散发性 Creutzfeldt-Jakob 病:104 例回顾性分析。
Eur Neurol. 2020;83(1):65-72. doi: 10.1159/000507189. Epub 2020 Apr 28.
3
Sensitivity and specificity evaluation of multiple neurodegenerative proteins for Creutzfeldt-Jakob disease diagnosis using a deep-learning approach.使用深度学习方法评估多种神经退行性蛋白在克雅氏病诊断中的敏感性和特异性。
Prion. 2019 Jan;13(1):141-150. doi: 10.1080/19336896.2019.1639482.
4
Quality evaluation for the surveillance system of human prion diseases in China based on the data from 2010 to 2016.基于2010年至2016年数据的中国人类朊病毒病监测系统质量评估
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本文引用的文献

1
Evidence-based guideline: diagnostic accuracy of CSF 14-3-3 protein in sporadic Creutzfeldt-Jakob disease: report of the guideline development subcommittee of the American Academy of Neurology.循证指南:脑脊液 14-3-3 蛋白在散发性克雅氏病中的诊断准确性:美国神经病学学会指南制定小组委员会的报告。
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Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.1997-2008 年阿根廷克雅氏病监测。
Neuroepidemiology. 2011;37(3-4):193-202. doi: 10.1159/000331907. Epub 2011 Nov 5.
3
High sensitivity of an ELISA kit for detection of the gamma-isoform of 14-3-3 proteins: usefulness in laboratory diagnosis of human prion disease.酶联免疫吸附测定试剂盒检测 14-3-3 蛋白γ-异构体的高灵敏度:在人类朊病毒病实验室诊断中的应用价值。
BMC Neurol. 2011 Oct 4;11:120. doi: 10.1186/1471-2377-11-120.
4
The epidemiological, clinical, and laboratory features of sporadic Creutzfeldt-Jakob disease patients in China: surveillance data from 2006 to 2010.中国散发性克雅氏病患者的流行病学、临床和实验室特征:2006 年至 2010 年监测数据。
PLoS One. 2011;6(8):e24231. doi: 10.1371/journal.pone.0024231. Epub 2011 Aug 31.
5
Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK.诊断变异型克雅氏病:英国前 150 例病例的回顾性分析。
J Neurol Neurosurg Psychiatry. 2011 Jun;82(6):646-51. doi: 10.1136/jnnp.2010.232264. Epub 2010 Dec 15.
6
Prospective 10-year surveillance of human prion diseases in Japan.日本朊病毒病前瞻性 10 年监测。
Brain. 2010 Oct;133(10):3043-57. doi: 10.1093/brain/awq216. Epub 2010 Sep 20.
7
[Prion disease--the characteristics and diagnostic points in Japan].[朊病毒病——日本的特征及诊断要点]
Rinsho Shinkeigaku. 2010 May;50(5):287-300. doi: 10.5692/clinicalneurol.50.287.
8
Incidence of Creutzfeldt-Jakob disease in Taiwan: a prospective 10-year surveillance.台湾克雅氏病的发病率:一项前瞻性的 10 年监测。
Eur J Epidemiol. 2010 May;25(5):341-7. doi: 10.1007/s10654-010-9446-4. Epub 2010 Mar 24.
9
[Epidemiological surveillance of Creutzfeldt-Jakob in France].[法国克雅氏病的流行病学监测]
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10
Diagnostic value of CSF protein profile in a Portuguese population of sCJD patients.脑脊液蛋白质谱在葡萄牙散发性克雅氏病患者群体中的诊断价值。
J Neurol. 2009 Sep;256(9):1540-50. doi: 10.1007/s00415-009-5160-0. Epub 2009 May 6.

脑脊液中14-3-3蛋白阳性的疑似克雅氏病韩国患者的特征:韩国克雅氏病主动监测项目的初步研究

Characteristics of Korean patients with suspected Creutzfeldt-Jakob disease with 14-3-3 protein in cerebrospinal fluid: Preliminary study of the Korean Creutzfeldt-Jakob disease active surveillance program.

作者信息

Lim Jae-Sung, Kwon Hyung-Min, Jang Jae-Won, Ju Young-Ran, Kim SuYeon, Park Young Ho, Park So Young, Kim SangYun

机构信息

a Department of Neurology ; Seoul National University Boramae Hospital ; Seoul , South Korea ;

出版信息

Prion. 2015;9(2):136-43. doi: 10.1080/19336896.2015.1022020.

DOI:10.1080/19336896.2015.1022020
PMID:25996401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4601202/
Abstract

Although Korea had a national surveillance system for Creutzfeldt-Jakob disease (CJD), it was mainly dependent on attending physician's reports. Thus, little prospective data about the epidemiology, characteristics, and final diagnoses of suspected patients were available. We have established a nationwide network for the active surveillance of patients with suspected CJD. When the requested cerebrospinal fluid (CSF) samples tested positive for 14-3-3 protein, we investigated the clinical characteristics of the corresponding patients and followed them until their final diagnoses were confirmed. A total of 218 samples were requested for CSF assays from May 2010 to August 2012, and 106 (48.6%) were positive for 14-3-3 protein. In 89 patients with complete clinical data, 38 (42.7%) were diagnosed with probable CJD and the estimated annual occurrence of CJD was 16.3 persons-per-year. The most common diagnoses of the remainder were central nervous system infection and any-cause encephalopathy. Non-CJD subjects showed worse initial consciousness levels than CJD patients. This preliminary study showed that the number of reported cases of CJD and the true positivity rates of CSF 14-3-3 protein assays were both low in Korea. An active surveillance system is urgently needed to provide the latest nationwide epidemiological data of CJD.

摘要

尽管韩国有克雅氏病(CJD)国家监测系统,但该系统主要依赖主治医生的报告。因此,关于疑似患者的流行病学、特征及最终诊断的前瞻性数据很少。我们建立了一个全国性网络,用于对疑似克雅氏病患者进行主动监测。当所要求的脑脊液(CSF)样本14-3-3蛋白检测呈阳性时,我们调查了相应患者的临床特征,并对他们进行跟踪,直至其最终诊断得到确认。2010年5月至2012年8月期间,共要求对218份样本进行脑脊液检测,其中106份(48.6%)14-3-3蛋白检测呈阳性。在89例有完整临床数据的患者中,38例(42.7%)被诊断为可能的克雅氏病,克雅氏病的估计年发病率为每年16.3人。其余患者最常见的诊断为中枢神经系统感染和不明原因脑病。非克雅氏病患者的初始意识水平比克雅氏病患者差。这项初步研究表明,韩国克雅氏病报告病例数和脑脊液14-3-3蛋白检测的实际阳性率均较低。迫切需要一个主动监测系统来提供克雅氏病最新的全国流行病学数据。