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Chinese Specific Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 57 Cases

OBJECTIVE: Sporadic Creutzfeldt-Jakob disease (sCJD) is a fatal and transmissible neurodegenerative disorder. However, no studies have reported Chinese specific characteristics of sCJD. We aimed to identify differences in sCJD between Chinese patients and patients from other countries. METHODS: The...

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Autores principales: Zhao, Wei, Zhang, Jia-Tang, Xing, Xiao-Wei, Huang, De-Hui, Tian, Cheng-Lin, Jia, Wei-Quan, Huang, Xu-Sheng, Wu, Wei-Ping, Pu, Chuan-Qiang, Lang, Sen-Yang, Yu, Sheng-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597718/
https://www.ncbi.nlm.nih.gov/pubmed/23516482
http://dx.doi.org/10.1371/journal.pone.0058442
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author Zhao, Wei
Zhang, Jia-Tang
Xing, Xiao-Wei
Huang, De-Hui
Tian, Cheng-Lin
Jia, Wei-Quan
Huang, Xu-Sheng
Wu, Wei-Ping
Pu, Chuan-Qiang
Lang, Sen-Yang
Yu, Sheng-Yuan
author_facet Zhao, Wei
Zhang, Jia-Tang
Xing, Xiao-Wei
Huang, De-Hui
Tian, Cheng-Lin
Jia, Wei-Quan
Huang, Xu-Sheng
Wu, Wei-Ping
Pu, Chuan-Qiang
Lang, Sen-Yang
Yu, Sheng-Yuan
author_sort Zhao, Wei
collection PubMed
description OBJECTIVE: Sporadic Creutzfeldt-Jakob disease (sCJD) is a fatal and transmissible neurodegenerative disorder. However, no studies have reported Chinese specific characteristics of sCJD. We aimed to identify differences in sCJD between Chinese patients and patients from other countries. METHODS: The data from 57 Chinese sCJD patients were retrospectively analyzed, including demographic data, clinical manifestations, laboratory examinations, electroencephalograms (EEGs), diffusion-weighted imaging (DWI) scans, positron emission tomography (PET) scans, and pathological results. RESULT: The disease was pathologically confirmed in 11 patients. 39 cases were diagnosed as probable sCJD, and 7 were possible. Of the total cases, 33 were male, and 24 were female. The onset age ranged from 36 to 75 years (mean: 55.5, median: 57). Disease onset before the age of 60 occurred in 57.9% of patients. The disease duration from onset to death ranged 5–22 months (mean: 11.6, median: 11), and 51.9% of patients died 7 to 12 months after disease onset. The majority of patients presented with sub-acute onset with progressive dementia. 3 of the 9 patients who took 14-3-3 protein analysis had positive results (33.3%). The sensitivity of EEG was 79.6% (43/54). For DWI and PET examinations, the sensitivities were 94% (47/50) and 94.1% (16/17), respectively. In seven patients who did not show typical hyper-intensities on the first DWI examination, abnormalities of hypo-metabolism in the cerebral cortex were clearly detected by PET. In 13 out of the 17 patients, PET detected extra abnormal regions in addition to the hyper-intense areas observed in DWI. CONCLUSION: This is the first study to indicate that Chinese sCJD patients have a much earlier onset age and a longer disease duration than other populations, which is most likely related to racial differences. The longer disease duration may also be a probable characteristic of Asian populations. PET had high sensitivity for the diagnosis of sCJD.
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spelling pubmed-35977182013-03-20 Chinese Specific Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 57 Cases Zhao, Wei Zhang, Jia-Tang Xing, Xiao-Wei Huang, De-Hui Tian, Cheng-Lin Jia, Wei-Quan Huang, Xu-Sheng Wu, Wei-Ping Pu, Chuan-Qiang Lang, Sen-Yang Yu, Sheng-Yuan PLoS One Research Article OBJECTIVE: Sporadic Creutzfeldt-Jakob disease (sCJD) is a fatal and transmissible neurodegenerative disorder. However, no studies have reported Chinese specific characteristics of sCJD. We aimed to identify differences in sCJD between Chinese patients and patients from other countries. METHODS: The data from 57 Chinese sCJD patients were retrospectively analyzed, including demographic data, clinical manifestations, laboratory examinations, electroencephalograms (EEGs), diffusion-weighted imaging (DWI) scans, positron emission tomography (PET) scans, and pathological results. RESULT: The disease was pathologically confirmed in 11 patients. 39 cases were diagnosed as probable sCJD, and 7 were possible. Of the total cases, 33 were male, and 24 were female. The onset age ranged from 36 to 75 years (mean: 55.5, median: 57). Disease onset before the age of 60 occurred in 57.9% of patients. The disease duration from onset to death ranged 5–22 months (mean: 11.6, median: 11), and 51.9% of patients died 7 to 12 months after disease onset. The majority of patients presented with sub-acute onset with progressive dementia. 3 of the 9 patients who took 14-3-3 protein analysis had positive results (33.3%). The sensitivity of EEG was 79.6% (43/54). For DWI and PET examinations, the sensitivities were 94% (47/50) and 94.1% (16/17), respectively. In seven patients who did not show typical hyper-intensities on the first DWI examination, abnormalities of hypo-metabolism in the cerebral cortex were clearly detected by PET. In 13 out of the 17 patients, PET detected extra abnormal regions in addition to the hyper-intense areas observed in DWI. CONCLUSION: This is the first study to indicate that Chinese sCJD patients have a much earlier onset age and a longer disease duration than other populations, which is most likely related to racial differences. The longer disease duration may also be a probable characteristic of Asian populations. PET had high sensitivity for the diagnosis of sCJD. Public Library of Science 2013-03-14 /pmc/articles/PMC3597718/ /pubmed/23516482 http://dx.doi.org/10.1371/journal.pone.0058442 Text en © 2013 Zhao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhao, Wei
Zhang, Jia-Tang
Xing, Xiao-Wei
Huang, De-Hui
Tian, Cheng-Lin
Jia, Wei-Quan
Huang, Xu-Sheng
Wu, Wei-Ping
Pu, Chuan-Qiang
Lang, Sen-Yang
Yu, Sheng-Yuan
Chinese Specific Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 57 Cases
title Chinese Specific Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 57 Cases
title_full Chinese Specific Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 57 Cases
title_fullStr Chinese Specific Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 57 Cases
title_full_unstemmed Chinese Specific Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 57 Cases
title_short Chinese Specific Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 57 Cases
title_sort chinese specific characteristics of sporadic creutzfeldt-jakob disease: a retrospective analysis of 57 cases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597718/
https://www.ncbi.nlm.nih.gov/pubmed/23516482
http://dx.doi.org/10.1371/journal.pone.0058442
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