National TSE Reference Center, Department of Neurology, Georg-August University Goettingen, Robert-Koch-Strasse 40, Goettingen, Germany.
Brain. 2009 Oct;132(Pt 10):2659-68. doi: 10.1093/brain/awp191. Epub 2009 Sep 22.
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroencephalogram and cerebrospinal fluid biomarkers have been reported to support clinical diagnosis but with variable utility according to subtype. In recent years, a series of publications have demonstrated a potentially important role for magnetic resonance imaging in the pre-mortem diagnosis of sporadic Creutzfeldt-Jakob disease. Magnetic resonance imaging signal alterations correlate with distinct sporadic Creutzfeldt-Jakob disease molecular subtypes and thus might contribute to the earlier identification of the whole spectrum of sporadic Creutzfeldt-Jakob disease cases. This multi-centre international study aimed to provide a rationale for the amendment of the clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Patients with sporadic Creutzfeldt-Jakob disease and fluid attenuated inversion recovery or diffusion-weight imaging were recruited from 12 countries. Patients referred as 'suspected sporadic Creutzfeldt-Jakob disease' but with an alternative diagnosis after thorough follow up, were analysed as controls. All magnetic resonance imaging scans were assessed for signal changes according to a standard protocol encompassing seven cortical regions, basal ganglia, thalamus and cerebellum. Magnetic resonance imaging scans were evaluated in 436 sporadic Creutzfeldt-Jakob disease patients and 141 controls. The pattern of high signal intensity with the best sensitivity and specificity in the differential diagnosis of sporadic Creutzfeldt-Jakob disease was identified. The optimum diagnostic accuracy in the differential diagnosis of rapid progressive dementia was obtained when either at least two cortical regions (temporal, parietal or occipital) or both caudate nucleus and putamen displayed a high signal in fluid attenuated inversion recovery or diffusion-weight imaging magnetic resonance imaging. Based on our analyses, magnetic resonance imaging was positive in 83% of cases. In all definite cases, the amended criteria would cover the vast majority of suspected cases, being positive in 98%. Cerebral cortical signal increase and high signal in caudate nucleus and putamen on fluid attenuated inversion recovery or diffusion-weight imaging magnetic resonance imaging are useful in the diagnosis of sporadic Creutzfeldt-Jakob disease. We propose an amendment to the clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease to include findings from magnetic resonance imaging scans.
已经确定了散发性克雅氏病的几种分子亚型,并且已经报道了脑电图和脑脊液生物标志物来支持临床诊断,但根据亚型的不同,其效用也有所不同。近年来,一系列出版物表明磁共振成像在散发性克雅氏病的生前诊断中具有潜在的重要作用。磁共振成像信号改变与不同的散发性克雅氏病分子亚型相关,因此可能有助于更早地识别散发性克雅氏病的整个谱系。这项多中心国际研究旨在为修订散发性克雅氏病的临床诊断标准提供依据。从 12 个国家招募了患有散发性克雅氏病且进行了液体衰减反转恢复或弥散加权成像的患者。经过彻底随访后被诊断为“疑似散发性克雅氏病”但具有其他诊断的患者被作为对照进行分析。根据包括七个皮质区域、基底节、丘脑和小脑的标准方案,对所有磁共振成像扫描进行信号改变评估。对 436 例散发性克雅氏病患者和 141 例对照进行了磁共振成像扫描评估。确定了在散发性克雅氏病鉴别诊断中具有最佳敏感性和特异性的高信号强度模式。在快速进展性痴呆的鉴别诊断中获得最佳诊断准确性时,当至少两个皮质区域(颞叶、顶叶或枕叶)或两个尾状核和壳核在液体衰减反转恢复或弥散加权成像磁共振成像中显示高信号时。基于我们的分析,磁共振成像在 83%的病例中呈阳性。在所有明确的病例中,修订后的标准将涵盖绝大多数疑似病例,阳性率为 98%。大脑皮质信号增加和尾状核和壳核在液体衰减反转恢复或弥散加权成像磁共振成像中的高信号对散发性克雅氏病的诊断有用。我们建议对散发性克雅氏病的临床诊断标准进行修订,纳入磁共振成像扫描结果。