期刊文献+

弥散加权磁共振(DWI)异常可作为Creutzfeldt-Jakob病(CJD)的一个早期诊断指标 被引量:1

Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease
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摘要 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 byDWI.Ninewere definite based on theWorld Health Organization criteria, and 27 were probable. The percentages ofDWI 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 patientswho did not showPSWCs on the first EEG, abnormalDWI findings were still clearly detec ted. 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 dia gnosis of CJD; consideration should be given to its inclusion in the clinical diagnostic criteria of CJD. 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 byDWI.Ninewere definite based on theWorld Health Organization criteria, and 27 were probable. The percentages ofDWI 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 patientswho did not showPSWCs on the first EEG, abnormalDWI findings were still clearly detec ted. 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 dia gnosis of CJD; consideration should be given to its inclusion in the clinical diagnostic criteria of CJD.
出处 《世界核心医学期刊文摘(神经病学分册)》 2005年第1期45-46,共2页 Digest of the World Core Medical Journals:Clinical Neurology
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