Literature DB >> 18303557

Early detection of periodic sharp wave complexes on EEG by independent component analysis in patients with Creutzfeldt-Jakob disease.

Po-Shan Wang1, Yu-Te Wu, Chih-I Hung, Shan-Yeong Kwan, Shin Teng, Bing-Wen Soong.   

Abstract

Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common human prion disease. EEG is the method of choice to support the diagnosis of a human prion disease. Periodic sharp wave complexes (PSWCs) on the EEG usually indicate a progressive stage of CJD. However, PSWCs only become obvious at around 8 to 12 weeks after the onset of clinical symptoms, and in a few cases, even later. Independent component analysis (ICA) is a new technique to separate statistically independent components from a mixture of data. This study recruited seven patients who fit the criteria of CJD between 2002 and 2005 and 10 patients with Alzheimer's disease (AD) as control subjects. Using an ICA algorithm, we were able to split typical PSWCs into several independent temporal components in conjunction with spatial maps. The PSWCs were not observed in the initial EEG studies of patients with either AD or CJD. However, the ICA algorithm was able to extract periodic discharges and epileptiform discharges from raw EEG of patients with CJD at as early as 3 to 5 weeks after disease onset. Such discharges otherwise could hardly be discerned by visual inspection. In conclusion, ICA may increase the sensitivity of EEG and facilitate the early diagnosis of CJD.

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Year:  2008        PMID: 18303557     DOI: 10.1097/WNP.0b013e318163a7d5

Source DB:  PubMed          Journal:  J Clin Neurophysiol        ISSN: 0736-0258            Impact factor:   2.177


  6 in total

1.  Transmissible spongiform encephalopathies with P102L mutation of PRNP manifesting different phenotypes: clinical, neuroimaging, and electrophysiological studies in Chinese kindred in Taiwan.

Authors:  Nai-Fang Chi; Yi-Chung Lee; Yi-Chun Lu; Hsiu-Mei Wu; Bing-Wen Soong
Journal:  J Neurol       Date:  2009-08-21       Impact factor: 4.849

2.  Three sporadic cases of Creutzfeldt-Jakob disease in China and their clinical analysis.

Authors:  Xingbang Wang; Na Li; Aifen Liu; Lin Ma; Peiyan Shan; Wenjing Jiang; Qun Zhang
Journal:  Exp Ther Med       Date:  2017-07-25       Impact factor: 2.447

3.  Sensitivity and specificity evaluation of multiple neurodegenerative proteins for Creutzfeldt-Jakob disease diagnosis using a deep-learning approach.

Authors:  Sol Moe Lee; Jae Wook Hyeon; Soo-Jin Kim; Heebal Kim; Ran Noh; Seonghan Kim; Yeong Seon Lee; Su Yeon Kim
Journal:  Prion       Date:  2019-01       Impact factor: 3.931

4.  Report of a Case of Creutzfeldt-Jakob Disease With an Unusual Quick Evolution.

Authors:  Hajar Fadili; Rim Tazi; Hiba El Oury; Karim El Aidaoui; Asmaa Hazim
Journal:  Cureus       Date:  2022-03-09

5.  Impairment of cerebellar long-term depression and GABAergic transmission in prion protein deficient mice ectopically expressing PrPLP/Dpl.

Authors:  Yasushi Kishimoto; Moritoshi Hirono; Ryuichiro Atarashi; Suehiro Sakaguchi; Tohru Yoshioka; Shigeru Katamine; Yutaka Kirino
Journal:  Sci Rep       Date:  2020-09-28       Impact factor: 4.379

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

Authors:  Taiki Matsubayashi; Miho Akaza; Yuichi Hayashi; Tsuyoshi Hamaguchi; Masahito Yamada; Takayoshi Shimohata; Takanori Yokota; Nobuo Sanjo
Journal:  Prion       Date:  2020-12       Impact factor: 3.931

  6 in total

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