局灶尖波是散发性克雅氏病mm2 -皮质形式的特异性早期标志物。

IF 1.9 3区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Prion Pub Date : 2020-12-01 DOI:10.1080/19336896.2020.1803516
Taiki Matsubayashi, Miho Akaza, Yuichi Hayashi, Tsuyoshi Hamaguchi, Masahito Yamada, Takayoshi Shimohata, Takanori Yokota, Nobuo Sanjo
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引用次数: 3

摘要

周期性尖锐波复合体(PSWCs),通过脑电图识别,在不到一半的散发性克雅氏病(sCJD)的蛋氨酸纯合型2型皮质(MM2c)型患者中观察到,并且仅在疾病的后期阶段。在这项研究中,我们在MM2c-sCJD患者的脑电图(eeg)上发现了早期和特异性标记物。我们回顾性研究了诊断为sCJD的患者的临床记录、脑电图和磁共振成像(MRI)扫描,并比较了MM2c-sCJD组和MM1/经典sCJD组的脑电图表现。纳入6例MM2c-sCJD和8例MM1/经典sCJD的记录。MM2c-组和MM1/经典sCJD组的中位发病年龄分别为75.0岁(范围60-83岁)和72.5岁(范围51-74岁),发病至首次脑电图的平均持续时间分别为9.17个月(范围4-15个月)和1.88个月(范围1-4个月)。在疾病进展早期的MM2c-sCJD患者的脑电图上发现了与MRI扫描的皮质高强度相对应的脑区域的局灶尖波和/或局灶尖波复合物。相比之下,早期MM1/典型sCJD患者的脑电图显示偏侧或广泛性弥漫性尖波和峰波复合物,其不局限于MRI扫描发现的皮质高强度。我们的研究结果表明,MM2c-sCJD早期患者脑电图上的局灶尖波和/或局灶尖波复合物是该疾病的特征,这表明该特征可能对早期诊断有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Focal sharp waves are a specific early-stage marker of the MM2-cortical form of sporadic Creutzfeldt-Jakob disease.

Periodic sharp wave complexes (PSWCs), identified using electroencephalography, are observed in less than half of patients with the methionine homozygosity type 2 cortical (MM2c) form of sporadic Creutzfeldt-Jakob disease (sCJD), and only at a later stage of the disease. In this study, we identified early and specific markers on the electroencephalograms (EEGs) of patients with MM2c-sCJD. We retrospectively investigated the clinical records, EEGs, and magnetic resonance imaging (MRI) scans of patients diagnosed with sCJD and compared the EEG findings of MM2c-sCJD and MM1/classic sCJD groups. The records of six patients with MM2c-sCJD and eight with MM1/classic sCJD were included. The median ages of onset in the MM2c- and MM1/classic sCJD groups were 75.0 (range, 60-83) and 72.5 (range, 51-74) years, respectively, and the average durations between disease onset and the first EEG were 9.17 (range, 4-15) and 1.88 (range, 1-4) months, respectively. Focal sharp waves and/or focal spike-and-wave complexes in the brain regions corresponding with cortical hyperintensities on MRI scans were identified on the EEGs of patients with MM2c-sCJD in the early stages of disease progression. In contrast, EEGs of patients in the early stages of MM1/classic sCJD showed lateralized or generalized diffuse sharp waves and spike-and-wave complexes, which were not limited to cortical hyperintensities identified with MRI scans. Our findings indicate that focal sharp waves and/or focal spike-and-wave complexes on the EEGs of patients in the early phase of MM2c-sCJD are characteristic of the disease, suggesting the possible usefulness of this characteristic for early diagnosis.

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来源期刊
Prion
Prion 生物-生化与分子生物学
CiteScore
5.20
自引率
4.30%
发文量
13
审稿时长
6-12 weeks
期刊介绍: Prion is the first international peer-reviewed open access journal to focus exclusively on protein folding and misfolding, protein assembly disorders, protein-based and structural inheritance. The goal is to foster communication and rapid exchange of information through timely publication of important results using traditional as well as electronic formats. The overriding criteria for publication in Prion are originality, scientific merit and general interest.
期刊最新文献
A systemic analysis of Creutzfeldt Jakob disease cases in Asia. Mutations in human prion-like domains: pathogenic but not always amyloidogenic. Prion forensics: a multidisciplinary approach to investigate CWD at an illegal deer carcass disposal site. Exploring CJD incidence trends: insights from Slovakia. Unmet needs of biochemical biomarkers for human prion diseases.
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