Literature DB >> 20051687

Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images.

Kazuo Mutsukura1, Katsuya Satoh, Susumu Shirabe, Itsuro Tomita, Takayasu Fukutome, Minoru Morikawa, Masachika Iseki, Kensuke Sasaki, Yusei Shiaga, Tetsuyuki Kitamoto, Katsumi Eguchi.   

Abstract

BACKGROUND: Diffusion-weighted imaging (DWI) has been reported to be a useful technique for diagnosing Creutzfeldt-Jakob disease (CJD). The present study reported DWI results in cases of familial CJD with a V180I mutation (CJD180) in the prion protein gene as well as neurological findings.
METHODS: A retrospective analysis of 3 patients with V180I was performed. Cerebrospinal fluid (CSF) analysis, brain MRI, single-photon emission computed tomography (SPECT), and magnetic resonance spectroscopy (MRS) were included. CSF was analyzed for biochemical markers, and each patient underwent brain MRI, SPECT, and MRS analysis. A brain biopsy from the frontal cortex, which corresponded to the area of increased DWI signals, was utilized for neuropathological analysis.
RESULTS: CSF analysis results revealed elevated total tau protein and the absence of 14-3-3 protein, as well as decreased concentrations of neuron-specific enolase, S100 protein, and prostaglandin E(2). All patients presented with unique MRI features. Brain biopsy showed severe spongiform morphology, but comparatively preserved neurons and mild astrocytic gliosis. Accumulations of PrP(Sc) were not detected using the 3F4 antibody, and microglial activation was subtle. SPECT revealed hypoperfusion throughout both hemispheres. MRS revealed a reduced N-acetyl aspartate/creatine ratio.
CONCLUSION: Results from this study suggested that increased DWI signals could reflect severe spongiform changes in CJD180 patients.

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Year:  2009        PMID: 20051687      PMCID: PMC2837892          DOI: 10.1159/000254842

Source DB:  PubMed          Journal:  Dement Geriatr Cogn Disord        ISSN: 1420-8008            Impact factor:   2.959


  17 in total

1.  Prion protein deposits match magnetic resonance imaging signal abnormalities in Creutzfeldt-Jakob disease.

Authors:  Stéphane Haïk; Didier Dormont; Baptiste A Faucheux; Claude Marsault; Jean-Jacques Hauw
Journal:  Ann Neurol       Date:  2002-06       Impact factor: 10.422

2.  Combined diffusion-weighted and spectroscopic MR imaging in Creutzfeldt-Jakob disease.

Authors:  C C Tchoyoson Lim; Kevin Tan; Kamal K Verma; Hong Yin; N Venketasubramanian
Journal:  Magn Reson Imaging       Date:  2004-06       Impact factor: 2.546

3.  Diffusion-weighted MR imaging in biopsy-proven Creutzfeldt-Jakob disease.

Authors:  H C Kim; K H Chang; I C Song; S H Lee; B J Kwon; M H Han; S Y Kim
Journal:  Korean J Radiol       Date:  2001 Oct-Dec       Impact factor: 3.500

4.  Brain biopsy in patients with suspected Creutzfeldt-Jakob disease.

Authors:  Uta Heinemann; Anna Krasnianski; Bettina Meissner; Kai Kallenberg; Hans A Kretzschmar; Walter Schulz-Schaeffer; Inga Zerr
Journal:  J Neurosurg       Date:  2008-10       Impact factor: 5.115

5.  Magnetic resonance spectroscopic abnormalities in sporadic and variant Creutzfeldt-Jakob disease.

Authors:  H G Pandya; S C Coley; I D Wilkinson; P D Griffiths
Journal:  Clin Radiol       Date:  2003-02       Impact factor: 2.350

Review 6.  [Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles].

Authors:  Y Iwaski; M Sone; T Kato; E Yoshida; T Indo; M Yoshida; Y Hashizume; M Yamada
Journal:  Rinsho Shinkeigaku       Date:  1999-08

7.  [An autopsy-verified case of Creutzfeldt-Jakob disease with codon 129 polymorphism and codon 180 point mutation].

Authors:  T Matsumura; S Kojima; Y Kuroiwa; A Takagi; M Unakami; T Kitamoto
Journal:  Rinsho Shinkeigaku       Date:  1995-03

8.  Pathologic correlates of diffusion MRI changes in Creutzfeldt-Jakob disease.

Authors:  D N Manners; P Parchi; C Tonon; S Capellari; R Strammiello; C Testa; G Tani; E Malucelli; C Spagnolo; P Cortelli; P Montagna; R Lodi; B Barbiroli
Journal:  Neurology       Date:  2009-04-21       Impact factor: 9.910

9.  A discrepancy between Tc-99m HMPAO SPECT and Tc-99m ECD SPECT in Creutzfeldt-Jacob disease.

Authors:  Ichiro Sunada; Toru Ishida; Shinichi Sakamoto; Naohiro Tsuyuguchi
Journal:  J Clin Neurosci       Date:  2004-08       Impact factor: 1.961

10.  Clinical features of Creutzfeldt-Jakob disease with V180I mutation.

Authors:  K Jin; Y Shiga; S Shibuya; K Chida; Y Sato; H Konno; K Doh-ura; T Kitamoto; Y Itoyama
Journal:  Neurology       Date:  2004-02-10       Impact factor: 9.910

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  14 in total

Review 1.  Clinical Laboratory Tests Used To Aid in Diagnosis of Human Prion Disease.

Authors:  Allyson Connor; Han Wang; Brian S Appleby; Daniel D Rhoads
Journal:  J Clin Microbiol       Date:  2019-09-24       Impact factor: 5.948

2.  Do prion protein gene polymorphisms induce apoptosis in non-mammals?

Authors:  Tuğçe Birkan; Mesut Şahin; Zubeyde Öztel; Erdal Balcan
Journal:  J Biosci       Date:  2016-03       Impact factor: 1.826

3.  Creutzfeldt-Jakob Disease with a prion protein gene codon 180 mutation presenting asymmetric cortical high-intensity on magnetic resonance imaging.

Authors:  Yuko Amano; Noriyuki Kimura; Takuya Hanaoka; Yasuhiro Aso; Teruyuki Hirano; Hiroyuki Murai; Katsuya Satoh; Etsuro Matsubara
Journal:  Prion       Date:  2015       Impact factor: 3.931

4.  Pathogenic mutations in the hydrophobic core of the human prion protein can promote structural instability and misfolding.

Authors:  Marc W van der Kamp; Valerie Daggett
Journal:  J Mol Biol       Date:  2010-10-07       Impact factor: 5.469

5.  Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.

Authors:  Qi Shi; Xiao-Jing Shen; Wei Zhou; Kang Xiao; Xiao-Mei Zhang; Bao-Yun Zhang; Xiao-Ping Dong
Journal:  Prion       Date:  2014       Impact factor: 3.931

6.  Discriminant analysis of prion sequences for prediction of susceptibility.

Authors:  Ji-Hae Lee; Se-Eun Bae; Sunghoon Jung; Insung Ahn; Hyeon Seok Son
Journal:  Exp Mol Med       Date:  2013-10-11       Impact factor: 8.718

Review 7.  Prions in variably protease-sensitive prionopathy: an update.

Authors:  Wen-Quan Zou; Pierluigi Gambetti; Xiangzhu Xiao; Jue Yuan; Jan Langeveld; Laura Pirisinu
Journal:  Pathogens       Date:  2013-07-05

8.  White matter involvement in sporadic Creutzfeldt-Jakob disease.

Authors:  Eduardo Caverzasi; Maria Luisa Mandelli; Stephen J DeArmond; Christopher P Hess; Paolo Vitali; Nico Papinutto; Abby Oehler; Bruce L Miller; Irina V Lobach; Stefano Bastianello; Michael D Geschwind; Roland G Henry
Journal:  Brain       Date:  2014-11-02       Impact factor: 13.501

9.  Spreading brain lesions in a familial Creutzfeldt-Jakob disease with V180I mutation over 4 years.

Authors:  Kentaro Deguchi; Motonori Takamiya; Shoko Deguchi; Nobutoshi Morimoto; Tomoko Kurata; Yoshio Ikeda; Koji Abe
Journal:  BMC Neurol       Date:  2012-11-24       Impact factor: 2.474

10.  Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.

Authors:  Temu Qina; Nobuo Sanjo; Masaki Hizume; Maya Higuma; Makoto Tomita; Ryuichiro Atarashi; Katsuya Satoh; Ichiro Nozaki; Tsuyoshi Hamaguchi; Yosikazu Nakamura; Atsushi Kobayashi; Tetsuyuki Kitamoto; Shigeo Murayama; Hiroyuki Murai; Masahito Yamada; Hidehiro Mizusawa
Journal:  BMJ Open       Date:  2014-05-16       Impact factor: 2.692

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