Literature DB >> 16235047

Characteristic signal changes in the pontine base on T2- and multishot diffusion-weighted images in spinocerebellar ataxia type 1.

M Adachi1, T Kawanami, H Ohshima, T Hosoya.   

Abstract

The aim of the present study was to demonstrate characteristic signal changes of the pontine base on T2-weighted images of patients with SCA 1, and to elucidate the relationship between abnormal high-intensities of the pontine base on T2-weighted images and the findings on multishot diffusion-weighted images. We assessed abnormal signals of the pontine base on T2-weighted images from 50 controls and six patients with SCA 1 diagnosed by genetic analysis. At the same time, we evaluated the degeneration of the transverse pontine fibers in the pontine base by multishot diffusion-weighted imaging. A midline high-intensity was seen in the pontine base on T2-weighted images in two of the 50 controls and five of the six patients with SCA 1. The midline high-intensity had a sensitivity of 83.3% for patients and a specificity of 96.0% for controls. Multishot diffusion-weighted imaging demonstrated the degeneration--the amorphous-pattern signal--of the transverse pontine fibers in four (66.7%) of the six patients. In the other two patients, the zebra-pattern signal was seen in the pontine base. The midline high-intensity on T2-weighted images appears to be one of characteristic MRI findings of SCA 1. Multishot diffusion-weighted imaging suggested that the midline high-intensity should reflect the degeneration of the transverse pontine fibers.

Entities:  

Mesh:

Year:  2005        PMID: 16235047     DOI: 10.1007/s00234-005-0002-y

Source DB:  PubMed          Journal:  Neuroradiology        ISSN: 0028-3940            Impact factor:   2.804


  27 in total

1.  Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).

Authors:  Z Matsuyama; H Kawakami; H Maruyama; Y Izumi; O Komure; F Udaka; M Kameyama; T Nishio; Y Kuroda; M Nishimura; S Nakamura
Journal:  Hum Mol Genet       Date:  1997-08       Impact factor: 6.150

2.  Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.

Authors:  K Bürk; M Abele; M Fetter; J Dichgans; M Skalej; F Laccone; O Didierjean; A Brice; T Klockgether
Journal:  Brain       Date:  1996-10       Impact factor: 13.501

3.  Proton magnetic resonance spectroscopy in an Italian family with spinocerebellar ataxia type 1.

Authors:  M Mascalchi; M Tosetti; R Plasmati; M C Bianchi; C Tessa; F Salvi; M Frontali; F Valzania; C Bartolozzi; C A Tassinari
Journal:  Ann Neurol       Date:  1998-02       Impact factor: 10.422

4.  [Magnetic resonance studies of dentato-rubro-pallido-luysian atrophy--correlation with clinical severity and age of onset].

Authors:  H Otsuka; M Harada; M Hieda; M Takahashi; K Miyoshi; M Miyazaki; I Kondoh; H Nishitani
Journal:  No To Shinkei       Date:  1996-09

5.  Clinical features and natural history of multiple system atrophy. An analysis of 100 cases.

Authors:  G K Wenning; Y Ben Shlomo; M Magalhães; S E Daniel; N P Quinn
Journal:  Brain       Date:  1994-08       Impact factor: 13.501

6.  Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findings.

Authors:  R Koide; O Onodera; T Ikeuchi; R Kondo; H Tanaka; S Tokiguchi; A Tomoda; T Miike; F Isa; H Beppu; N Shimizu; Y Watanabe; Y Horikawa; T Shimohata; K Hirota; A Ishikawa; S Tsuji
Journal:  Neurology       Date:  1997-12       Impact factor: 9.910

7.  Regional differences in genetic subgroup frequency in hereditary cerebellar ataxia, and a morphometrical study of brain MR images in SCA1, MJD and SCA6.

Authors:  U Nagaoka; Y Suzuki; T Kawanami; K Kurita; Y Shikama; K Honda; K Abe; T Nakajima; T Kato
Journal:  J Neurol Sci       Date:  1999-04-01       Impact factor: 3.181

8.  Characteristic magnetic resonance imaging findings in Machado-Joseph disease.

Authors:  Y Murata; S Yamaguchi; H Kawakami; Y Imon; H Maruyama; T Sakai; T Kazuta; T Ohtake; M Nishimura; T Saida; S Chiba; T Oh-i; S Nakamura
Journal:  Arch Neurol       Date:  1998-01

9.  [Clinical types of spinocerebellar degeneration and evaluation with MR imaging].

Authors:  S Kojima
Journal:  Rinsho Shinkeigaku       Date:  1993-12

10.  Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p.

Authors:  S Nagafuchi; H Yanagisawa; K Sato; T Shirayama; E Ohsaki; M Bundo; T Takeda; K Tadokoro; I Kondo; N Murayama
Journal:  Nat Genet       Date:  1994-01       Impact factor: 38.330

View more
  5 in total

1.  Magnetic resonance imaging in spinocerebellar ataxias.

Authors:  Susanne Döhlinger; Till-Karsten Hauser; Johannes Borkert; Andreas R Luft; Jörg B Schulz
Journal:  Cerebellum       Date:  2008       Impact factor: 3.847

Review 2.  Magnetic resonance imaging biomarkers in patients with progressive ataxia: current status and future direction.

Authors:  Stuart Currie; Marios Hadjivassiliou; Ian J Craven; Iain D Wilkinson; Paul D Griffiths; Nigel Hoggard
Journal:  Cerebellum       Date:  2013-04       Impact factor: 3.847

Review 3.  The extra-cerebellar effects of spinocerebellar ataxia type 1 (SCA1): looking beyond the cerebellum.

Authors:  Victor Olmos; Neha Gogia; Kimberly Luttik; Fatema Haidery; Janghoo Lim
Journal:  Cell Mol Life Sci       Date:  2022-07-08       Impact factor: 9.207

4.  Diffusion tensor imaging of spinocerebellar ataxias types 1 and 2.

Authors:  M L Mandelli; T De Simone; L Minati; M G Bruzzone; C Mariotti; R Fancellu; M Savoiardo; M Grisoli
Journal:  AJNR Am J Neuroradiol       Date:  2007 Nov-Dec       Impact factor: 3.825

5.  Visualization of brain white matter tracts using heavily t2-weighted three-dimensional fluid-attenuated inversion-recovery magnetic resonance imaging.

Authors:  Masahiro Yamazaki; Shinji Naganawa; Kiminori Bokura; Hisashi Kawai
Journal:  Nagoya J Med Sci       Date:  2014-08       Impact factor: 1.131

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.