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Evidence of axonal damage in cerebellar peduncles without T2-lesions in multiple sclerosis.
Hannoun, Salem; Kocevar, Gabriel; Durand-Dubief, Françoise; Stamile, Claudio; Naji, Amal; Cotton, Francois; Cavallari, Michele; Guttmann, Charles R G; Sappey-Marinier, Dominique.
Afiliação
  • Hannoun S; CREATIS, UMR 5220 CNRS & U1206 INSERM, Université Claude Bernard - Lyon1, Université de Lyon, Villeurbanne, France; Nehme and Therese Tohme Multiple Sclerosis Center, Faculty of Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
  • Kocevar G; CREATIS, UMR 5220 CNRS & U1206 INSERM, Université Claude Bernard - Lyon1, Université de Lyon, Villeurbanne, France.
  • Durand-Dubief F; CREATIS, UMR 5220 CNRS & U1206 INSERM, Université Claude Bernard - Lyon1, Université de Lyon, Villeurbanne, France; Service de Neurologie A, Hôpital Neurologique Pierre Wertheimer, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France.
  • Stamile C; CREATIS, UMR 5220 CNRS & U1206 INSERM, Université Claude Bernard - Lyon1, Université de Lyon, Villeurbanne, France.
  • Naji A; Nehme and Therese Tohme Multiple Sclerosis Center, Faculty of Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
  • Cotton F; CREATIS, UMR 5220 CNRS & U1206 INSERM, Université Claude Bernard - Lyon1, Université de Lyon, Villeurbanne, France; Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon, Pierre Bénite, France.
  • Cavallari M; Center for Neurological Imaging, Partners Multiple Sclerosis Center, Departments of Neurology and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Guttmann CRG; Center for Neurological Imaging, Partners Multiple Sclerosis Center, Departments of Neurology and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: guttmann@bwh.harvard.edu.
  • Sappey-Marinier D; CREATIS, UMR 5220 CNRS & U1206 INSERM, Université Claude Bernard - Lyon1, Université de Lyon, Villeurbanne, France; Département IRM, CERMEP-Imagerie du Vivant, Université de Lyon, Bron, France. Electronic address: dominique.sappey-marinier@univ-lyon1.fr.
Eur J Radiol ; 108: 114-119, 2018 Nov.
Article em En | MEDLINE | ID: mdl-30396642
BACKGROUND AND AIM: Cerebellar peduncles (CP) can be probed by diffusion tensor imaging (DTI) to evaluate the integrity of cerebellar afferent and efferent networks. Damage to the CP in multiple sclerosis (MS) could lead to serious cognitive and mobility impairment. The aim of this study was to investigate the extent and the clinical impact of CP damage in MS. METHODS: Sixty-eight MS patients were included in this study along with 27 healthy controls (HC) and underwent an MRI on a 1.5T including T1, T2, FLAIR and DTI. Using DTI, the microstructural integrity within the CP regions (superior (SCP), inferior (ICP) and middle (MCP)) was probed while controlling for focal T2-lesions presence or absence. A general linear model was performed to test for associations between clinical scores and DTI metrics for each CP. RESULTS: Significantly decreased fractional anisotropy (FA) and increased radial diffusivity (RD) were found in the CP of all MS patients compared to those of HC, but to a lesser extent in non-lesioned CP than those with lesions. Axial diffusivity (AD) was significantly and similarly increased in both non-lesioned and lesioned CP, but only in the SCP and ICP. Expanded disability status scale (EDSS) significantly correlated with MCP's FA (p < 0.05) and RD (p < 0.05), while MS functional composite (MSFC) significantly correlated with SCP's FA (p < 0.01) and RD (p < 0.01). CONCLUSION: The diffusion changes (FA and RD) measured in lesioned CP are probably directly related to the presence of inflammatory and/or demyelinating lesions. In contrast, the microstructural alterations reflected by AD increase in non-lesioned CP may result either from remote effects of cerebral white matter injury (diaschisis) or primary axonal degeneration, that are associated with cognitive, sensory and motor impairments of MS patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Substância Branca / Esclerose Múltipla Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Eur J Radiol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Líbano País de publicação: Irlanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Substância Branca / Esclerose Múltipla Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Eur J Radiol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Líbano País de publicação: Irlanda