Gray matter and white matter changes in non-demented amyotrophic lateral sclerosis patients with or without cognitive impairment: A combined voxel-based morphometry and tract-based spatial statistics whole-brain analysis.

The phenotypic heterogeneity in amyotrophic lateral sclerosis (ALS) implies that patients show structural changes within but also beyond the motor cortex and corticospinal tract and furthermore outside the frontal lobes, even if frank dementia is not detected. The aim of the present study was to inv...

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Publicado en:Brain Imaging & Behavior Vol. 12; no. 2; pp. 547 - 564
Autores principales: Christidi, Foteini, Karavasilis, Efstratios, Riederer, Franz, Zalonis, Ioannis, Ferentinos, Panagiotis, Velonakis, Georgios, Xirou, Sophia, Rentzos, Michalis, Argiropoulos, Georgios, Zouvelou, Vasiliki, Zambelis, Thomas, Athanasakos, Athanasios, Toulas, Panagiotis, Vadikolias, Konstantinos, Efstathopoulos, Efstathios, Kollias, Spyros, Karandreas, Nikolaos, Kelekis, Nikolaos, Evdokimidis, Ioannis
Formato: research Journal Article
Publicado: Springer Nature Apr2018
Acceso en línea:Ver este registro en EBSCOhost
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      pub: Springer Nature
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        atl: Gray matter and white matter changes in non-demented amyotrophic lateral sclerosis patients with or without cognitive impairment: A combined voxel-based morphometry and tract-based spatial statistics whole-brain analysis.
      aug:
        au:
          Christidi, Foteini
          Karavasilis, Efstratios
          Riederer, Franz
          Zalonis, Ioannis
          Ferentinos, Panagiotis
          Velonakis, Georgios
          Xirou, Sophia
          Rentzos, Michalis
          Argiropoulos, Georgios
          Zouvelou, Vasiliki
          Zambelis, Thomas
          Athanasakos, Athanasios
          Toulas, Panagiotis
          Vadikolias, Konstantinos
          Efstathopoulos, Efstathios
          Kollias, Spyros
          Karandreas, Nikolaos
          Kelekis, Nikolaos
          Evdokimidis, Ioannis
        affil: First Department of Neurology, Aeginition Hospital, Medical School, National & Kapodistrian University, Athens, Greece
      sug:
        subj:
          Amyotrophic Lateral Sclerosis Psychosocial Factors
          Amyotrophic Lateral Sclerosis
          Brain
          Gray Matter Pathology
          Magnetic Resonance Imaging
          Body Weights and Measures
          Neuroradiography
          Human
          Middle Age
          Diagnostic Imaging
          Brain Pathology
          Male
          Amyotrophic Lateral Sclerosis Pathology
          Models, Statistical
          Female
          Imaging, Three-Dimensional
          Gray Matter
          Validation Studies
          Comparative Studies
          Evaluation Research
          Multicenter Studies
          Middle Aged: 45-64 years
          Male
          Female
      ab: The phenotypic heterogeneity in amyotrophic lateral sclerosis (ALS) implies that patients show structural changes within but also beyond the motor cortex and corticospinal tract and furthermore outside the frontal lobes, even if frank dementia is not detected. The aim of the present study was to investigate both gray matter (GM) and white matter (WM) changes in non-demented amyotrophic lateral sclerosis (ALS) patients with or without cognitive impairment (ALS-motor and ALS-plus, respectively). Nineteen ALS-motor, 31 ALS-plus and 25 healthy controls (HC) underwent 3D-T1-weighted and 30-directional diffusion-weighted imaging on a 3 T MRI scanner. Voxel-based morphometry and tract-based spatial-statistics analysis were performed to examine GM volume (GMV) changes and WM differences in fractional anisotropy (FA), axial and radial diffusivity (AD, RD, respectively). Compared to HC, ALS-motor patients showed decreased GMV in frontal and cerebellar areas and increased GMV in right supplementary motor area, while ALS-plus patients showed diffuse GMV reduction in primary motor cortex bilaterally, frontotemporal areas, cerebellum and basal ganglia. ALS-motor patients had increased GMV in left precuneus compared to ALS-plus patients. We also found decreased FA and increased RD in the corticospinal tract bilaterally, the corpus callosum and extra-motor tracts in ALS-motor patients, and decreased FA and increased AD and RD in motor and several WM tracts in ALS-plus patients, compared to HC. Multimodal neuroimaging confirms motor and extra-motor GM and WM abnormalities in non-demented cognitively-impaired ALS patients (ALS-plus) and identifies early extra-motor brain pathology in ALS patients without cognitive impairment (ALS-motor).
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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