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本文引用的文献

1
Thalamo-striatal diffusion reductions precede disease onset in prion mutation carriers.丘脑纹状体弥散减少先于朊病毒突变携带者发病。
Brain. 2009 Oct;132(Pt 10):2680-7. doi: 10.1093/brain/awp064. Epub 2009 Mar 24.
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
MR imaging of familial Creutzfeldt-Jakob disease: a blinded and controlled study.家族性克雅氏病的磁共振成像:一项盲法对照研究。
AJNR Am J Neuroradiol. 2008 Oct;29(9):1638-43. doi: 10.3174/ajnr.A1217. Epub 2008 Jul 17.
4
Does the presentation of Creutzfeldt-Jakob disease vary by age or presumed etiology? A meta-analysis of the past 10 years.克雅氏病的临床表现是否因年龄或推测病因而异?对过去10年的一项荟萃分析。
J Neuropsychiatry Clin Neurosci. 2007 Fall;19(4):428-35. doi: 10.1176/jnp.2007.19.4.428.
5
First symptom in sporadic Creutzfeldt-Jakob disease.散发性克雅氏病的首发症状。
Neurology. 2006 Jan 24;66(2):286-7. doi: 10.1212/01.wnl.0000196440.00297.67.
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Psychiatric manifestations of Creutzfeldt-Jakob disease: a 25-year analysis.克雅氏病的精神症状:一项为期25年的分析。
J Neuropsychiatry Clin Neurosci. 2005 Fall;17(4):489-95. doi: 10.1176/jnp.17.4.489.
7
Sporadic and familial CJD: classification and characterisation.散发性和家族性克雅氏病:分类与特征
Br Med Bull. 2003;66:213-39. doi: 10.1093/bmb/66.1.213.
8
AN ATAXIC FORM OF SUBACUTE PRESENILE POLIOENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE).一种亚急性早老性脑脊髓病(克雅氏病)的共济失调型
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9
Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies.格斯特曼-施特劳斯勒-谢inker综合征、致死性家族性失眠症和库鲁病:对这些较罕见的人类可传播性海绵状脑病的综述
J Clin Neurosci. 2001 Sep;8(5):387-97. doi: 10.1054/jocn.2001.0919.
10
The FAB: a Frontal Assessment Battery at bedside.FAB:一种床边额叶评估量表。
Neurology. 2000 Dec 12;55(11):1621-6. doi: 10.1212/wnl.55.11.1621.

克雅氏病(CJD)神经状态量表:一种用于评估疾病严重程度和进展的新工具。

The Creutzfeldt-Jakob disease (CJD) neurological status scale: a new tool for evaluation of disease severity and progression.

机构信息

Department of Neurology and the Sagol Neuroscience Center, Tel-Hashomer, Israel.

出版信息

Acta Neurol Scand. 2011 Dec;124(6):368-74. doi: 10.1111/j.1600-0404.2011.01489.x. Epub 2011 Feb 8.

DOI:10.1111/j.1600-0404.2011.01489.x
PMID:21303352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3100358/
Abstract

OBJECTIVES

To develop a scale sensitive for the neurological manifestations of Creutzfeldt-Jakob disease (CJD).

METHODS

A 26-item CJD neurological status scale (CJD-NS) was created based on characteristic disease manifestations. Each sign was assigned to one of eight neurological systems to calculate a total scale score (TSS) and a system involvement score (SIS). The scale was administered to 37 CJD patients, 101 healthy first-degree relatives of the patients and 14 elderly patients with Parkinson's disease (PD).

RESULTS

The mean TSS (±SD) was significantly higher in patients with CJD (13.19 ± 5.63) compared with normal controls (0.41 ± 0.78) and PD patients (9.71 ± 3.05). The mean SIS was also significantly different between the CJD (5.19 ± 1.22) and PD (2.78 ± 1.18 P ≤ 0.01) groups reflecting the disseminated nature of neurological involvement in CJD. Using a cutoff of TSS > 4 yielded a sensitivity of 97% for CJD, and specificity of 100% against healthy controls. All individual items showed excellent specificity against healthy subjects, but sensitivity was highly variable. Repeat assessments of CJD patients over 3-9 months revealed a time-dependent increase in both the TSS and the SIS reflecting the scale's ability to track disease progression.

CONCLUSIONS

The CJD-NS scale is sensitive to neurological signs and their progression in CJD patients.

摘要

目的

开发一种针对克雅氏病(CJD)神经表现的量表。

方法

根据特征性疾病表现,创建了 26 项克雅氏病神经状态量表(CJD-NS)。每个体征被分配到八个神经系统之一,以计算总评分(TSS)和系统受累评分(SIS)。该量表对 37 名 CJD 患者、101 名患者的健康一级亲属和 14 名帕金森病(PD)老年患者进行了评估。

结果

与正常对照组(0.41 ± 0.78)和 PD 患者(9.71 ± 3.05)相比,CJD 患者的平均 TSS(±SD)明显更高(13.19 ± 5.63)。CJD(5.19 ± 1.22)和 PD(2.78 ± 1.18,P ≤ 0.01)组之间的平均 SIS 也存在显著差异,反映了 CJD 神经受累的弥散性质。使用 TSS > 4 的截止值可使 CJD 的敏感性达到 97%,特异性达到 100%,对健康对照人群具有特异性。所有单项指标对健康受试者均具有极佳的特异性,但敏感性差异很大。对 CJD 患者进行 3-9 个月的重复评估显示,TSS 和 SIS 均随时间呈上升趋势,表明该量表能够跟踪疾病进展。

结论

CJD-NS 量表对 CJD 患者的神经体征及其进展敏感。