Literature DB >> 23221952

Microstructural integrity of cerebral fiber tracts in hereditary spastic paraparesis with SPG11 mutation.

M-K Pan1, S-C Huang, Y-C Lo, Chih-Chao Yang, T-W Cheng, Chi-Cheng Yang, M-S Hua, M-J Lee, W-Y I Tseng.   

Abstract

BACKGROUND AND
PURPOSE: ARHSP-TCC is characterized by progressive leg spasticity, ataxia, and cognitive dysfunction. Although mutations in the human SPG11 gene were identified as responsible for ARHSP-TCC, the cerebral fiber integrity has not been assessed systemically. The objective of this study was to assess cerebral fiber integrity and its clinical significance in patients with ARHSP-TCC.
MATERIALS AND METHODS: Five patients from 2 families who were clinically and genetically confirmed to have ARHSP-TCC were examined by neuropsychological evaluation and DSI of the brain. We performed voxel-based GFA analysis for global white matter evaluation, tractography-based analysis for tract-to-tract comparisons, and tract-specific analysis of the CST to evaluate microstructural integrity along the axonal direction.
RESULTS: The neuropsychological evaluation revealed widespread cognitive decline across all domains. Voxel-based analysis showed global reduction of GFA in the cerebral white matter. Tractography-based analysis revealed a significant reduction of the microstructural integrity in all neural fiber types, while commissure and association fibers had more GFA reduction than projection fibers (P < .00001). Prefrontal and motor portions of the CC were most severely affected among all fiber tracts (P < .00001, P = .018). Tract-specific analysis of the CST validated a "dying-back" phenomenon (R(2) = 0.68, P < .00001).
CONCLUSIONS: There was a characteristic gradation in the reduction of microstructural integrity among fiber types and within the CC in patients with the SPG11 mutation. The dying-back process in CST might explain the pathogenic mechanisms for ARHSP-TCC.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 23221952      PMCID: PMC7964653          DOI: 10.3174/ajnr.A3330

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  32 in total

1.  Tract-specific and region of interest analysis of corticospinal tract integrity in subcortical ischemic stroke: reliability and correlation with motor function of affected lower extremity.

Authors:  P-F Tang; Y-H Ko; Z-A Luo; F-C Yeh; S-H A Chen; W-Y I Tseng
Journal:  AJNR Am J Neuroradiol       Date:  2010-01-28       Impact factor: 3.825

2.  Q-ball imaging.

Authors:  David S Tuch
Journal:  Magn Reson Med       Date:  2004-12       Impact factor: 4.668

Review 3.  Axon degeneration mechanisms: commonality amid diversity.

Authors:  Michael Coleman
Journal:  Nat Rev Neurosci       Date:  2005-11       Impact factor: 34.870

4.  Diffusion spectrum magnetic resonance imaging (DSI) tractography of crossing fibers.

Authors:  V J Wedeen; R P Wang; J D Schmahmann; T Benner; W Y I Tseng; G Dai; D N Pandya; P Hagmann; H D'Arceuil; A J de Crespigny
Journal:  Neuroimage       Date:  2008-04-08       Impact factor: 6.556

5.  The loss of asymmetry and reduced interhemispheric connectivity in adolescents with autism: a study using diffusion spectrum imaging tractography.

Authors:  Yu-Chun Lo; Wei-Tsuen Soong; Susan Shur-Fen Gau; Yu-Yu Wu; Meng-Chuan Lai; Fang-Cheng Yeh; Wen-Yang Chiang; Li-Wei Kuo; Fu-Shan Jaw; Wen-Yih Isaac Tseng
Journal:  Psychiatry Res       Date:  2011-03-05       Impact factor: 3.222

6.  Diffusion tensor imaging of two unrelated Chinese men with hereditary spastic paraplegia associated with thin corpus callosum.

Authors:  Qin Chen; Su Lui; Jian-Gang Wang; Luo Ou-Yang; Dong Zhou; Jean-Marc Burgunder; Qi-Yong Gong; Hui-Fang Shang
Journal:  Neurosci Lett       Date:  2008-06-07       Impact factor: 3.046

7.  Validation of diffusion spectrum magnetic resonance imaging with manganese-enhanced rat optic tracts and ex vivo phantoms.

Authors:  Ching-Po Lin; Van Jay Wedeen; Jyh-Horng Chen; Ching Yao; Wen-Yih Isaac Tseng
Journal:  Neuroimage       Date:  2003-07       Impact factor: 6.556

Review 8.  [Pre-postoperative neuropsychological evaluation in the surgical treatment of epilepsy].

Authors:  P Campo; J León-Carrión; J M Domínguez-Roldán; M Revuelta; F Murillo-Cabezas
Journal:  Rev Neurol       Date:  1998-10       Impact factor: 0.870

9.  Hereditary spastic paraplegia with a thin corpus callosum and thalamic involvement in Japan.

Authors:  M Ueda; Y Katayama; T Kamiya; M Mishina; H Igarashi; S Okubo; M Senda; K Iwabuchi; A Terashi
Journal:  Neurology       Date:  1998-12       Impact factor: 9.910

10.  Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.

Authors:  Giovanni Stevanin; Filippo M Santorelli; Hamid Azzedine; Paula Coutinho; Jacques Chomilier; Paola S Denora; Elodie Martin; Anne-Marie Ouvrard-Hernandez; Alessandra Tessa; Naïma Bouslam; Alexander Lossos; Perrine Charles; José L Loureiro; Nizar Elleuch; Christian Confavreux; Vítor T Cruz; Merle Ruberg; Eric Leguern; Djamel Grid; Meriem Tazir; Bertrand Fontaine; Alessandro Filla; Enrico Bertini; Alexandra Durr; Alexis Brice
Journal:  Nat Genet       Date:  2007-02-18       Impact factor: 38.330

View more
  4 in total

1.  White Matter Alterations in Spastic Paraplegia Type 5: A Multiparametric Structural MRI Study and Correlations with Biochemical Measurements.

Authors:  Y Liu; Z Ye; J Hu; Z Xiao; F Zhang; X Yang; W Chen; Y Fu; D Cao
Journal:  AJNR Am J Neuroradiol       Date:  2021-11-18       Impact factor: 3.825

2.  SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage.

Authors:  Ingrid Faber; Alberto Rolim Muro Martinez; Thiago Junqueira Ribeiro de Rezende; Carlos Roberto Martins; Melina Pazian Martins; Charles Marques Lourenço; Wilson Marques; Celeste Montecchiani; Antonio Orlacchio; Jose Luiz Pedroso; Orlando Graziani Povoas Barsottini; Íscia Lopes-Cendes; Marcondes Cavalcante França
Journal:  Neuroimage Clin       Date:  2018-06-09       Impact factor: 4.881

3.  Mild cognitive impairment in novel SPG11 mutation-related sporadic hereditary spastic paraplegia with thin corpus callosum: case series.

Authors:  Chuan Li; Qi Yan; Feng-Ju Duan; Chao Zhao; Zhuo Zhang; Ying Du; Wei Zhang
Journal:  BMC Neurol       Date:  2021-01-11       Impact factor: 2.474

4.  Neuropsychology and MRI correlates of neurodegeneration in SPG11 hereditary spastic paraplegia.

Authors:  Manuel Schmidt; Martin Regensburger; Kathrin S Utz; Zacharias Kohl; Dominique Cornelius Marterstock; Arnd Doerfler; Jürgen Winkler
Journal:  Orphanet J Rare Dis       Date:  2022-07-29       Impact factor: 4.303

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.