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Increased brain atrophy and lesion load is associated with stronger lower alpha MEG power in multiple sclerosis patients.
Van Schependom, Jeroen; Vidaurre, Diego; Costers, Lars; Sjøgård, Martin; Sima, Diana M; Smeets, Dirk; D'hooghe, Marie Beatrice; D'haeseleer, Miguel; Deco, Gustavo; Wens, Vincent; De Tiège, Xavier; Goldman, Serge; Woolrich, Mark; Nagels, Guy.
Afiliación
  • Van Schependom J; Neurology, Center for Neurosciences, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Laarbeeklaan 101, 1090 Brussels, Belgium; AIMS, Center for Neurosciences, Vrije Universiteit Brussel (VUB), Laarbeeklaan 103, 1090 Brussels, Belgium; Department of Electronics and Inf
  • Vidaurre D; Oxford Centre for Human Brain Activity (OHBA), University of Oxford, United Kingdom; Oxford University Centre for Functional MRI of the Brain (FMRIB), University of Oxford, United Kingdom; Center for Functionally Integrative Neuroscience, Department of Clinical Medicine, Aarhus University, Aarhus 80
  • Costers L; Neurology, Center for Neurosciences, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Laarbeeklaan 101, 1090 Brussels, Belgium; AIMS, Center for Neurosciences, Vrije Universiteit Brussel (VUB), Laarbeeklaan 103, 1090 Brussels, Belgium.
  • Sjøgård M; Laboratoire de Cartographie fonctionnelle du Cerveau, UNI-ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium.
  • Sima DM; icometrix NV, Kolonel Begaultlaan 1b / 12, 3012 Leuven, Belgium.
  • Smeets D; icometrix NV, Kolonel Begaultlaan 1b / 12, 3012 Leuven, Belgium.
  • D'hooghe MB; Neurology, Center for Neurosciences, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Laarbeeklaan 101, 1090 Brussels, Belgium; National MS Center Melsbroek, 1820 Melsbroek, Belgium.
  • D'haeseleer M; Neurology, Center for Neurosciences, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Laarbeeklaan 101, 1090 Brussels, Belgium; National MS Center Melsbroek, 1820 Melsbroek, Belgium.
  • Deco G; Computational Neuroscience Group, Universitat Pompeu Fabra, Spain.
  • Wens V; Laboratoire de Cartographie fonctionnelle du Cerveau, UNI-ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium; Magnetoencephalography Unit, Department of Functional Neuroimaging, Service of Nuclear Medicine, CUB-Hôpital Erasme, Brussels, Belgium.
  • De Tiège X; Laboratoire de Cartographie fonctionnelle du Cerveau, UNI-ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium; Magnetoencephalography Unit, Department of Functional Neuroimaging, Service of Nuclear Medicine, CUB-Hôpital Erasme, Brussels, Belgium.
  • Goldman S; Laboratoire de Cartographie fonctionnelle du Cerveau, UNI-ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Brussels, Belgium; Magnetoencephalography Unit, Department of Functional Neuroimaging, Service of Nuclear Medicine, CUB-Hôpital Erasme, Brussels, Belgium.
  • Woolrich M; Oxford Centre for Human Brain Activity (OHBA), University of Oxford, United Kingdom; Oxford University Centre for Functional MRI of the Brain (FMRIB), University of Oxford, United Kingdom.
  • Nagels G; Neurology, Center for Neurosciences, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Laarbeeklaan 101, 1090 Brussels, Belgium; AIMS, Center for Neurosciences, Vrije Universiteit Brussel (VUB), Laarbeeklaan 103, 1090 Brussels, Belgium; National MS Center Melsbroek, 182
Neuroimage Clin ; 30: 102632, 2021.
Article en En | MEDLINE | ID: mdl-33770549
ABSTRACT
In multiple sclerosis, the interplay of neurodegeneration, demyelination and inflammation leads to changes in neurophysiological functioning. This study aims to characterize the relation between reduced brain volumes and spectral power in multiple sclerosis patients and matched healthy subjects. During resting-state eyes closed, we collected magnetoencephalographic data in 67 multiple sclerosis patients and 47 healthy subjects, matched for age and gender. Additionally, we quantified different brain volumes through magnetic resonance imaging (MRI). First, a principal component analysis of MRI-derived brain volumes demonstrates that atrophy can be largely described by two components one overall degenerative component that correlates strongly with different cognitive tests, and one component that mainly captures degeneration of the cortical grey matter that strongly correlates with age. A multimodal correlation analysis indicates that increased brain atrophy and lesion load is accompanied by increased spectral power in the lower alpha (8-10 Hz) in the temporoparietal junction (TPJ). Increased lower alpha power in the TPJ was further associated with worse results on verbal and spatial working memory tests, whereas an increased lower/upper alpha power ratio was associated with slower information processing speed. In conclusion, multiple sclerosis patients with increased brain atrophy, lesion and thalamic volumes demonstrated increased lower alpha power in the TPJ and reduced cognitive abilities.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esclerosis Múltiple Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Neuroimage Clin Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esclerosis Múltiple Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Neuroimage Clin Año: 2021 Tipo del documento: Article