Literature DB >> 28278113

Clinical and laboratory features of 14 young Chinese probable sCJD patients.

Qi Shi1, Kang Xiao1, Cao Chen1, Wei Zhou1, Chen Gao1, Jing Wang1, Bao-Yun Zhang1, Yuan Wang1, Xiao-Ping Dong1.   

Abstract

Sporadic Creutzfeldt-Jakob disease (sCJD) occurs frequently in the relatively older population, mainly in the groups of 60-69 and 70-79 year-old. Since 2006 when China performed national CJD surveillance, 14 young probable sCJD patients below 40 year-old were identified, counting for 1.93% of all probable sCJD cases. The clinical features of young probable sCJD cases, including the onset feature, the presence of sCJD-associated signs and the clinical duration, are indistinguishable from those of older patients. Special sCJD-associated abnormalities on EEG and MRI were noticed in 7 and 10 cases. CSF 14-3-3 was positive in 7 cases. CSF RT-QuIC showed positive reactive curves in 9 cases, with short lag phases. PRNP sequencing did not find any mutation. Due to low rate of brain autopsy in China, performances of other CJD-associated examinations as much as possible are extremely important for the distinguish diagnosis of young probable sCJD patients.

Entities:  

Keywords:  Creutzfeldt-Jakob disease; prion disease; sporadic; surveillance; young patient

Mesh:

Substances:

Year:  2017        PMID: 28278113      PMCID: PMC5399906          DOI: 10.1080/19336896.2017.1287656

Source DB:  PubMed          Journal:  Prion        ISSN: 1933-6896            Impact factor:   3.931


  26 in total

1.  Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada.

Authors:  A Ladogana; M Puopolo; E A Croes; H Budka; C Jarius; S Collins; G M Klug; T Sutcliffe; A Giulivi; A Alperovitch; N Delasnerie-Laupretre; J-P Brandel; S Poser; H Kretzschmar; I Rietveld; E Mitrova; J de Pedro Cuesta; P Martinez-Martin; M Glatzel; A Aguzzi; R Knight; H Ward; M Pocchiari; C M van Duijn; R G Will; I Zerr
Journal:  Neurology       Date:  2005-05-10       Impact factor: 9.910

2.  Prospective 10-year surveillance of human prion diseases in Japan.

Authors:  Ichiro Nozaki; Tsuyoshi Hamaguchi; Nobuo Sanjo; Moeko Noguchi-Shinohara; Kenji Sakai; Yosikazu Nakamura; Takeshi Sato; Tetsuyuki Kitamoto; Hidehiro Mizusawa; Fumio Moriwaka; Yusei Shiga; Yoshiyuki Kuroiwa; Masatoyo Nishizawa; Shigeki Kuzuhara; Takashi Inuzuka; Masatoshi Takeda; Shigetoshi Kuroda; Koji Abe; Hiroyuki Murai; Shigeo Murayama; Jun Tateishi; Ichiro Takumi; Susumu Shirabe; Masafumi Harada; Atsuko Sadakane; Masahito Yamada
Journal:  Brain       Date:  2010-09-20       Impact factor: 13.501

3.  Creutzfeldt-Jakob disease in the United States, 1979-1994: using national mortality data to assess the possible occurrence of variant cases.

Authors:  R C Holman; A S Khan; E D Belay; L B Schonberger
Journal:  Emerg Infect Dis       Date:  1996 Oct-Dec       Impact factor: 6.883

4.  Intensity of human prion disease surveillance predicts observed disease incidence.

Authors:  Genevieve M J A Klug; Handan Wand; Marion Simpson; Alison Boyd; Matthew Law; Colin L Masters; Radoslav Matěj; Rachel Howley; Michael Farrell; Maren Breithaupt; Inga Zerr; Cornelia van Duijn; Carla Ibrahim-Verbaas; Jan Mackenzie; Robert G Will; Jean-Philippe Brandel; Annick Alperovitch; Herbert Budka; Gabor G Kovacs; Gerard H Jansen; Michael Coulthard; Steven J Collins
Journal:  J Neurol Neurosurg Psychiatry       Date:  2013-08-21       Impact factor: 10.154

Review 5.  Prions.

Authors:  S B Prusiner
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-10       Impact factor: 11.205

6.  Creutzfeldt-Jakob disease in an adolescent.

Authors:  J Monreal; G H Collins; C L Masters; C M Fisher; R C Kim; C J Gibbs; D C Gajdusek
Journal:  J Neurol Sci       Date:  1981 Nov-Dec       Impact factor: 3.181

7.  Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease.

Authors:  Lynne I McGuire; Alexander H Peden; Christina D Orrú; Jason M Wilham; Nigel E Appleford; Gary Mallinson; Mary Andrews; Mark W Head; Byron Caughey; Robert G Will; Richard S G Knight; Alison J E Green
Journal:  Ann Neurol       Date:  2012-08       Impact factor: 10.422

8.  Prion seeding activities of mouse scrapie strains with divergent PrPSc protease sensitivities and amyloid plaque content using RT-QuIC and eQuIC.

Authors:  Sarah Vascellari; Christina D Orrù; Andrew G Hughson; Declan King; Rona Barron; Jason M Wilham; Gerald S Baron; Brent Race; Alessandra Pani; Byron Caughey
Journal:  PLoS One       Date:  2012-11-05       Impact factor: 3.240

9.  Overview and evaluation of 15 years of Creutzfeldt-Jakob disease surveillance in Belgium, 1998-2012.

Authors:  Amber Litzroth; Patrick Cras; Bart De Vil; Sophie Quoilin
Journal:  BMC Neurol       Date:  2015-12-02       Impact factor: 2.474

Review 10.  Epidemiological characteristics of human prion diseases.

Authors:  Cao Chen; Xiao-Ping Dong
Journal:  Infect Dis Poverty       Date:  2016-06-02       Impact factor: 4.520

View more
  1 in total

1.  Analysis of Chinese patients with sporadic Creutzfeldt-Jakob disease.

Authors:  Jing Yang; Haiyan Kuang; Qiong Wang; Jiao Liu; Xueping Chen; Huifang Shang
Journal:  Prion       Date:  2020-12       Impact factor: 3.931

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.