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本文引用的文献

1
The role of cerebrospinal fluid proteins as early diagnostic markers for sporadic Creutzfeldt-Jakob disease.脑脊液蛋白作为散发性克雅氏病早期诊断标志物的作用。
Neurosci Lett. 2009 May 8;455(1):56-9. doi: 10.1016/j.neulet.2009.02.067. Epub 2009 Mar 5.
2
Characteristics of established and proposed sporadic Creutzfeldt-Jakob disease variants.已确定和提议的散发性克雅氏病变体的特征。
Arch Neurol. 2009 Feb;66(2):208-15. doi: 10.1001/archneurol.2008.533.
3
Rapidly progressive dementia.快速进展性痴呆
Ann Neurol. 2008 Jul;64(1):97-108. doi: 10.1002/ana.21430.
4
CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.脑脊液检测在克雅氏病鉴别诊断中的应用
Neurology. 2006 Aug 22;67(4):637-43. doi: 10.1212/01.wnl.0000230159.67128.00.
5
Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease.散发性克雅氏病临床谱中诊断性检查敏感性的决定因素。
Brain. 2006 Sep;129(Pt 9):2278-87. doi: 10.1093/brain/awl159. Epub 2006 Jul 1.
6
Diagnostic value of 14-3-3beta immunoblot and T-tau/P-tau ratio in clinically suspected Creutzfeldt-Jakob disease.14-3-3β免疫印迹及T-tau/P-tau比值在临床疑似克雅氏病中的诊断价值
Int J Mol Med. 2005 Dec;16(6):1147-9.
7
Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 type.散发性克雅氏病:罕见VV1型的临床及诊断特征
Neurology. 2005 Nov 22;65(10):1544-50. doi: 10.1212/01.wnl.0000184674.32924.c9. Epub 2005 Oct 12.
8
Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosis.克雅氏病的扩散加权成像和液体衰减反转恢复成像:诊断的高敏感性和特异性
AJNR Am J Neuroradiol. 2005 Jun-Jul;26(6):1551-62.
9
Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada.欧洲、澳大利亚和加拿大克雅氏病及相关疾病的死亡率。
Neurology. 2005 May 10;64(9):1586-91. doi: 10.1212/01.WNL.0000160117.56690.B2.
10
14-3-3 {gamma}-isoform detection distinguishes sporadic Creutzfeldt-Jakob disease from other dementias.14-3-3γ亚型检测可将散发性克雅氏病与其他痴呆症区分开来。
J Neurol Neurosurg Psychiatry. 2005 Jan;76(1):100-2. doi: 10.1136/jnnp.2003.032037.

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。

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.

机构信息

King Saud University, Riyadh, Saudi Arabia.

出版信息

Neurology. 2012 Oct 2;79(14):1499-506. doi: 10.1212/WNL.0b013e31826d5fc3. Epub 2012 Sep 19.

DOI:10.1212/WNL.0b013e31826d5fc3
PMID:22993290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3525296/
Abstract

OBJECTIVE

To assess the available evidence for the diagnostic accuracy of CSF testing for protein 14-3-3 in patients with suspected sporadic Creutzfeldt-Jakob disease (sCJD).

METHODS

The authors performed a systematic review of the available literature from 1995 to January 1, 2011, to identify articles involving patients who were suspected of having sCJD and who had CSF analysis for protein 14-3-3. Studies were rated according to the American Academy of Neurology classification of evidence scheme for diagnostic studies, and recommendations were linked to the strength of the evidence. A pooled estimate of sensitivity and specificity was obtained for all studies rated Class II or higher. The question asked is "Does CSF 14-3-3 protein accurately identify Creutzfeldt-Jakob disease (CJD) in patients with sCJD?"

RESULTS

The analysis was conducted on the basis of samples of 1,849 patients with suspected sCJD from 9 Class II studies. Assays for CSF 14-3-3 protein are probably moderately accurate in diagnosing sCJD: sensitivity 92% (95% confidence interval [CI] 89.8-93.6), specificity 80% (95% CI 77.4-83.0), likelihood ratio of 4.7, and negative likelihood ratio of 0.10.

RECOMMENDATION

For patients who have rapidly progressive dementia and are strongly suspected of having sCJD and for whom diagnosis remains uncertain (pretest probability ∼20%-90%), clinicians should order CSF 14-3-3 assays to reduce the uncertainty of the diagnosis (Level B).

摘要

目的

评估脑脊液蛋白 14-3-3 检测对疑似散发性克雅氏病(sCJD)患者的诊断准确性的现有证据。

方法

作者对 1995 年至 2011 年 1 月 1 日期间的现有文献进行了系统回顾,以确定涉及疑似 sCJD 且进行过脑脊液蛋白 14-3-3 分析的患者的文章。研究根据美国神经病学学会诊断研究证据分类方案进行评分,并根据证据的强度与推荐意见相关联。对所有评分达到 II 级或更高的研究进行汇总估计敏感性和特异性。提出的问题是“脑脊液 14-3-3 蛋白是否能准确识别 sCJD 患者的克雅氏病(CJD)?”

结果

该分析基于 9 项 II 级研究中 1849 例疑似 sCJD 患者的样本进行。脑脊液蛋白 14-3-3 检测对 sCJD 的诊断可能具有中等准确性:敏感性为 92%(95%置信区间 [CI] 89.8-93.6),特异性为 80%(95% CI 77.4-83.0),似然比为 4.7,阴性似然比为 0.10。

建议

对于那些快速进展性痴呆且强烈怀疑患有 sCJD 且诊断仍不确定的患者(先验概率约为 20%-90%),临床医生应开脑脊液蛋白 14-3-3 检测以降低诊断的不确定性(B 级)。