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扩散加权磁共振成像异常作为克雅氏病的早期诊断标志物

Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease.

作者信息

Shiga Y, Miyazawa K, Sato S, Fukushima R, Shibuya S, Sato Y, Konno H, Doh-ura K, Mugikura S, Tamura H, Higano S, Takahashi S, Itoyama Y

机构信息

Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Neurology. 2004 Aug 10;63(3):443-9. doi: 10.1212/01.wnl.0000134555.59460.5d.

Abstract

OBJECTIVE

To evaluate the usefulness of diffusion-weighted MRI (DWI) for the early diagnosis of Creutzfeldt-Jakob disease (CJD).

METHODS

Thirty-six consecutive patients (age 56 to 82 years) were enrolled, and 26 were examined by DWI. Nine were definite based on the World Health Organization criteria, and 27 were probable. The percentages of DWI abnormalities, periodic sharp wave complexes (PSWCs) on the EEG, detection of CSF 14-3-3 protein, and increase of CSF neuron-specific enolase (>25 ng/mL) on the first examination were compared. For DWI, 32 patients (age 31 to 84 years) who showed progressive dementia or impaired consciousness served as disease controls.

RESULTS

The percentage of DWI abnormalities was 92.3%, of PSWCs 50.0%, of 14-3-3 protein detection 84.0%, and of NSE increase 73.3%. Two of the 32 control subjects were falsely positive on DWI. The sensitivity of DWI was 92.3% (95% CI 74.8 to 99.5%) and specificity 93.8% (95% CI 79.2 to 99.2%). In 17 patients who did not show PSWCs on the first EEG, abnormal DWI findings were still clearly detected. Four patients who were negative for 14-3-3 protein also showed DWI abnormalities. DWI abnormalities were detected as early as at 3 weeks of symptom duration in four patients in whom PSWCs were not yet evident.

CONCLUSIONS

DWI can detect characteristic lesions in the majority of patients with CJD regardless of the presence of PSWCs. DWI was the most sensitive test for the early clinical diagnosis of CJD; consideration should be given to its inclusion in the clinical diagnostic criteria of CJD.

摘要

目的

评估弥散加权磁共振成像(DWI)在克雅氏病(CJD)早期诊断中的作用。

方法

纳入36例连续患者(年龄56至82岁),其中26例接受了DWI检查。根据世界卫生组织标准,9例为确诊病例,27例为疑似病例。比较首次检查时DWI异常的百分比、脑电图上的周期性尖锐波复合波(PSWC)、脑脊液14-3-3蛋白的检测以及脑脊液神经元特异性烯醇化酶升高(>25 ng/mL)的情况。对于DWI,选取32例表现为进行性痴呆或意识障碍的患者(年龄31至84岁)作为疾病对照。

结果

DWI异常的百分比为92.3%,PSWC为50.0%,14-3-3蛋白检测阳性为84.0%,NSE升高为73.3%。32例对照受试者中有2例DWI出现假阳性。DWI的敏感性为92.3%(95%可信区间74.8至99.5%),特异性为93.8%(95%可信区间79.2至99.2%)。在首次脑电图未显示PSWC的17例患者中,仍能清晰检测到DWI异常表现。4例14-3-3蛋白阴性的患者也显示出DWI异常。在4例PSWC尚不明显的患者中,症状出现3周时就检测到了DWI异常。

结论

无论是否存在PSWC,DWI均可在大多数CJD患者中检测到特征性病变。DWI是CJD早期临床诊断最敏感的检查方法;应考虑将其纳入CJD的临床诊断标准。

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