schliessen

Filtern

 

Bibliotheken

Surveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007

Background Human transmissible spongiform encephalopathies (HTSE), or Creutzfeldt-Jakob disease (CJD), is a group of rare and fatal diseases in central nervous system. Since outbreak of bovine spongiform encephalopathy (BSE) and variant CJD, a worldwide CJD surveillance network has been established... Full description

Journal Title: BMC Public Health 2008, Vol.8(1), p.360
Main Author: Shi, Qi
Other Authors: Gao, Chen , Zhou, Wei , Zhang, Bao-Yun , Chen, Jian-Ming , Tian, Chan , Jiang, Hui-Ying , Han, Jun , Xiang, Ni-Juan , Wang, Xiao-Fang , Gao, Yong-Jun , Dong, Xiao-Ping
Format: Electronic Article Electronic Article
Language:
Subjects:
ID: ISSN: 1471-2458 ; DOI: 10.1186/1471-2458-8-360 ; PMID: 18928564
Zum Text:
SendSend as email Add to Book BagAdd to Book Bag
Staff View
recordid: biomed_central1471-2458-8-360
title: Surveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007
format: Article
creator:
  • Shi, Qi
  • Gao, Chen
  • Zhou, Wei
  • Zhang, Bao-Yun
  • Chen, Jian-Ming
  • Tian, Chan
  • Jiang, Hui-Ying
  • Han, Jun
  • Xiang, Ni-Juan
  • Wang, Xiao-Fang
  • Gao, Yong-Jun
  • Dong, Xiao-Ping
subjects:
  • Public Health
ispartof: BMC Public Health, 2008, Vol.8(1), p.360
description: Background Human transmissible spongiform encephalopathies (HTSE), or Creutzfeldt-Jakob disease (CJD), is a group of rare and fatal diseases in central nervous system. Since outbreak of bovine spongiform encephalopathy (BSE) and variant CJD, a worldwide CJD surveillance network has been established under the proposition of WHO. In China, a national CJD surveillance system has started since 2002. The data of CJD surveillance from 2006 to 2007 was analyzed. Methods Total 12 provinces are included in CJD surveillance system. The surveillance unit in each province consists of one or two sentinel hospitals and the provincial CDC. All suspected CJD cases reported from CJD surveillance were diagnosed and subtyped based on the diagnostic criteria for CJD issued by WHO. Results Total 192 suspected CJD cases were reported and 5 genetic CJD, 51 probable and 30 possible sporadic CJD (sCJD) cases were diagnosed. The collected sCJD cases distribute sporadically without geographical clustering and seasonal relativity and the highest incidences in both probable and possible sCJD cases appeared in the group of 60–69 year. The most common three foremost symptoms were progressive dementia, cerebellum and mental-related symptoms. The probable sCJD patients owning both typical EEG alteration and CSF protein 14-3-3 positive have more characteristic clinical syndromes than the ones having only one positive. The polymorphisms of codon 129 of all tested reported cases shows typical patterns of Han Chinese as previous reports, that M129M are predominant whereas M129V are seldom. Conclusion Chinese CJD patients possessed similar epidemiological and clinical characteristics as worldwide.
language:
source:
identifier: ISSN: 1471-2458 ; DOI: 10.1186/1471-2458-8-360 ; PMID: 18928564
fulltext: fulltext
issn:
  • 1471-2458
  • 14712458
url: Link


@attributes
ID875805618
RANK0.07
NO1
SEARCH_ENGINEprimo_central_multiple_fe
SEARCH_ENGINE_TYPEPrimo Central Search Engine
LOCALfalse
PrimoNMBib
record
control
sourcerecordid1471-2458-8-360
sourceidbiomed_central
recordidTN_biomed_central1471-2458-8-360
sourceformatXML
sourcesystemPC
pqid69866826
display
typearticle
titleSurveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007
creatorShi, Qi ; Gao, Chen ; Zhou, Wei ; Zhang, Bao-Yun ; Chen, Jian-Ming ; Tian, Chan ; Jiang, Hui-Ying ; Han, Jun ; Xiang, Ni-Juan ; Wang, Xiao-Fang ; Gao, Yong-Jun ; Dong, Xiao-Ping
ispartofBMC Public Health, 2008, Vol.8(1), p.360
identifier
descriptionBackground Human transmissible spongiform encephalopathies (HTSE), or Creutzfeldt-Jakob disease (CJD), is a group of rare and fatal diseases in central nervous system. Since outbreak of bovine spongiform encephalopathy (BSE) and variant CJD, a worldwide CJD surveillance network has been established under the proposition of WHO. In China, a national CJD surveillance system has started since 2002. The data of CJD surveillance from 2006 to 2007 was analyzed. Methods Total 12 provinces are included in CJD surveillance system. The surveillance unit in each province consists of one or two sentinel hospitals and the provincial CDC. All suspected CJD cases reported from CJD surveillance were diagnosed and subtyped based on the diagnostic criteria for CJD issued by WHO. Results Total 192 suspected CJD cases were reported and 5 genetic CJD, 51 probable and 30 possible sporadic CJD (sCJD) cases were diagnosed. The collected sCJD cases distribute sporadically without geographical clustering and seasonal relativity and the highest incidences in both probable and possible sCJD cases appeared in the group of 60–69 year. The most common three foremost symptoms were progressive dementia, cerebellum and mental-related symptoms. The probable sCJD patients owning both typical EEG alteration and CSF protein 14-3-3 positive have more characteristic clinical syndromes than the ones having only one positive. The polymorphisms of codon 129 of all tested reported cases shows typical patterns of Han Chinese as previous reports, that M129M are predominant whereas M129V are seldom. Conclusion Chinese CJD patients possessed similar epidemiological and clinical characteristics as worldwide.
source
subjectPublic Health;
version6
lds50peer_reviewed
links
openurl$$Topenurl_article
openurlfulltext$$Topenurlfull_article
search
creatorcontrib
0Shi, Qi
1Gao, Chen
2Zhou, Wei
3Zhang, Bao-Yun
4Chen, Jian-Ming
5Tian, Chan
6Jiang, Hui-Ying
7Han, Jun
8Xiang, Ni-Juan
9Wang, Xiao-Fang
10Gao, Yong-Jun
11Dong, Xiao-Ping
titleSurveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007
descriptionAbstract Background Human transmissible spongiform encephalopathies (HTSE), or Creutzfeldt-Jakob disease (CJD), is a group of rare and fatal diseases in central nervous system. Since outbreak of bovine spongiform encephalopathy (BSE) and variant CJD, a worldwide CJD surveillance network has been established under the proposition of WHO. In China, a national CJD surveillance system has started since 2002. The data of CJD surveillance from 2006 to 2007 was analyzed. Methods Total 12 provinces are included in CJD surveillance system. The surveillance unit in each province consists of one or two sentinel hospitals and the provincial CDC. All suspected CJD cases reported from CJD surveillance were diagnosed and subtyped based on the diagnostic criteria for CJD issued by WHO. Results Total 192 suspected CJD cases were reported and 5 genetic CJD, 51 probable and 30 possible sporadic CJD (sCJD) cases were diagnosed. The collected sCJD cases distribute sporadically without geographical clustering and seasonal relativity and the highest incidences in both probable and possible sCJD cases appeared in the group of 60–69 year. The most common three foremost symptoms were progressive dementia, cerebellum and mental-related symptoms. The probable sCJD patients owning both typical EEG alteration and CSF protein 14-3-3 positive have more characteristic clinical syndromes than the ones having only one positive. The polymorphisms of codon 129 of all tested reported cases shows typical patterns of Han Chinese as previous reports, that M129M are predominant whereas M129V are seldom. Conclusion Chinese CJD patients possessed similar epidemiological and clinical characteristics as worldwide.
general
010.1186/1471-2458-8-360
118928564
sourceidbiomed_central
recordidbiomed_central1471-2458-8-360
issn
01471-2458
114712458
rsrctypearticle
creationdate2008
addtitleBMC Public Health
searchscope
0biomed_central
1FREE
2BioMed Central
scope
0biomed_central
1FREE
2BioMed Central
lsr30VSR-Enriched:[pages, pqid, subject]
sort
titleSurveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007
authorShi, Qi ; Gao, Chen ; Zhou, Wei ; Zhang, Bao-Yun ; Chen, Jian-Ming ; Tian, Chan ; Jiang, Hui-Ying ; Han, Jun ; Xiang, Ni-Juan ; Wang, Xiao-Fang ; Gao, Yong-Jun ; Dong, Xiao-Ping
creationdate20081018
facets
frbrgroupid8165979323300829228
frbrtype5
creationdate2008
collectionBioMed Central
prefilterarticles
rsrctypearticles
creatorcontrib
0Shi, Qi
1Gao, Chen
2Zhou, Wei
3Zhang, Bao-Yun
4Chen, Jian-Ming
5Tian, Chan
6Jiang, Hui-Ying
7Han, Jun
8Xiang, Ni-Juan
9Wang, Xiao-Fang
10Gao, Yong-Jun
11Dong, Xiao-Ping
jtitleBMC Public Health
toplevelpeer_reviewed
frbr
t2
k12008
k214712458
k310.1186/1471-2458-8-360
k48
k51
k6360
k7bmc public health
k8surveillance for creutzfeldt jakob disease in china from 2006 to 2007
k9surveillanceforcreuto2007
k12surveillanceforcreutzfeld
k15qishi
k16shiqi
delivery
delcategoryRemote Search Resource
fulltextfulltext
ranking
booster11
booster21
pcg_typeaggregator
addata
aulast
0Shi
1Gao
2Zhou
3Zhang
4Chen
5Tian
6Jiang
7Han
8Xiang
9Wang
10Dong
aufirst
0Qi
1Chen
2Wei
3Bao-Yun
4Jian-Ming
5Chan
6Hui-Ying
7Jun
8Ni-Juan
9Xiao-Fang
10Yong-Jun
11Xiao-Ping
au
0Shi, Qi
1Gao, Chen
2Zhou, Wei
3Zhang, Bao-Yun
4Chen, Jian-Ming
5Tian, Chan
6Jiang, Hui-Ying
7Han, Jun
8Xiang, Ni-Juan
9Wang, Xiao-Fang
10Gao, Yong-Jun
11Dong, Xiao-Ping
atitleSurveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007
jtitleBMC Public Health
volume8
issue1
spage360
issn1471-2458
formatarticle
genrearticle
ristypeJOUR
abstractAbstract Background Human transmissible spongiform encephalopathies (HTSE), or Creutzfeldt-Jakob disease (CJD), is a group of rare and fatal diseases in central nervous system. Since outbreak of bovine spongiform encephalopathy (BSE) and variant CJD, a worldwide CJD surveillance network has been established under the proposition of WHO. In China, a national CJD surveillance system has started since 2002. The data of CJD surveillance from 2006 to 2007 was analyzed. Methods Total 12 provinces are included in CJD surveillance system. The surveillance unit in each province consists of one or two sentinel hospitals and the provincial CDC. All suspected CJD cases reported from CJD surveillance were diagnosed and subtyped based on the diagnostic criteria for CJD issued by WHO. Results Total 192 suspected CJD cases were reported and 5 genetic CJD, 51 probable and 30 possible sporadic CJD (sCJD) cases were diagnosed. The collected sCJD cases distribute sporadically without geographical clustering and seasonal relativity and the highest incidences in both probable and possible sCJD cases appeared in the group of 60–69 year. The most common three foremost symptoms were progressive dementia, cerebellum and mental-related symptoms. The probable sCJD patients owning both typical EEG alteration and CSF protein 14-3-3 positive have more characteristic clinical syndromes than the ones having only one positive. The polymorphisms of codon 129 of all tested reported cases shows typical patterns of Han Chinese as previous reports, that M129M are predominant whereas M129V are seldom. Conclusion Chinese CJD patients possessed similar epidemiological and clinical characteristics as worldwide.
doi10.1186/1471-2458-8-360
pages360
oafree_for_read
date2008-10-18