Spatial distribution of multiple sclerosis lesions in the cervical spinal cord.


Journal

Brain : a journal of neurology
ISSN: 1460-2156
Titre abrégé: Brain
Pays: England
ID NLM: 0372537

Informations de publication

Date de publication:
01 03 2019
Historique:
received: 26 05 2018
revised: 25 10 2018
accepted: 20 11 2018
pubmed: 5 2 2019
medline: 7 1 2020
entrez: 5 2 2019
Statut: ppublish

Résumé

Spinal cord lesions detected on MRI hold important diagnostic and prognostic value for multiple sclerosis. Previous attempts to correlate lesion burden with clinical status have had limited success, however, suggesting that lesion location may be a contributor. Our aim was to explore the spatial distribution of multiple sclerosis lesions in the cervical spinal cord, with respect to clinical status. We included 642 suspected or confirmed multiple sclerosis patients (31 clinically isolated syndrome, and 416 relapsing-remitting, 84 secondary progressive, and 73 primary progressive multiple sclerosis) from 13 clinical sites. Cervical spine lesions were manually delineated on T2- and T2*-weighted axial and sagittal MRI scans acquired at 3 or 7 T. With an automatic publicly-available analysis pipeline we produced voxelwise lesion frequency maps to identify predilection sites in various patient groups characterized by clinical subtype, Expanded Disability Status Scale score and disease duration. We also measured absolute and normalized lesion volumes in several regions of interest using an atlas-based approach, and evaluated differences within and between groups. The lateral funiculi were more frequently affected by lesions in progressive subtypes than in relapsing in voxelwise analysis (P < 0.001), which was further confirmed by absolute and normalized lesion volumes (P < 0.01). The central cord area was more often affected by lesions in primary progressive than relapse-remitting patients (P < 0.001). Between white and grey matter, the absolute lesion volume in the white matter was greater than in the grey matter in all phenotypes (P < 0.001); however when normalizing by each region, normalized lesion volumes were comparable between white and grey matter in primary progressive patients. Lesions appearing in the lateral funiculi and central cord area were significantly correlated with Expanded Disability Status Scale score (P < 0.001). High lesion frequencies were observed in patients with a more aggressive disease course, rather than long disease duration. Lesions located in the lateral funiculi and central cord area of the cervical spine may influence clinical status in multiple sclerosis. This work shows the added value of cervical spine lesions, and provides an avenue for evaluating the distribution of spinal cord lesions in various patient groups.

Identifiants

pubmed: 30715195
pii: 5304670
doi: 10.1093/brain/awy352
pmc: PMC6391605
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

633-646

Subventions

Organisme : CIHR
ID : FDN-143263
Pays : Canada
Organisme : NINDS NIH HHS
ID : R21 NS087465
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY023240
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS078322
Pays : United States

Informations de copyright

© The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For permissions, please email: journals.permissions@oup.com.

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Auteurs

Dominique Eden (D)

NeuroPoly Lab, Institute of Biomedical Engineering, Polytechnique Montreal, Montreal, QC, Canada.

Charley Gros (C)

NeuroPoly Lab, Institute of Biomedical Engineering, Polytechnique Montreal, Montreal, QC, Canada.

Atef Badji (A)

NeuroPoly Lab, Institute of Biomedical Engineering, Polytechnique Montreal, Montreal, QC, Canada.
Department of Neuroscience, Faculty of Medicine, University of Montreal, Montreal, QC, Canada.

Sara M Dupont (SM)

NeuroPoly Lab, Institute of Biomedical Engineering, Polytechnique Montreal, Montreal, QC, Canada.
Department of Radiology and Biomedical Imaging, Zuckerberg San Francisco General Hospital, University of California, San Francisco, CA, USA.

Benjamin De Leener (B)

NeuroPoly Lab, Institute of Biomedical Engineering, Polytechnique Montreal, Montreal, QC, Canada.

Josefina Maranzano (J)

McConnell Brain Imaging Centre, Montreal Neurological Institute, Montreal, Canada.
Department of Anatomy, Université de Québec à Trois-Rivières, Trois-Rivières, QC, Canada.

Ren Zhuoquiong (R)

Department of Radiology, Xuanwu Hospital, Capital Medical University, Beijing, P. R. China.

Yaou Liu (Y)

Department of Radiology, Xuanwu Hospital, Capital Medical University, Beijing, P. R. China.
Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, P. R. China.

Tobias Granberg (T)

Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Massachusetts General Hospital, Boston, USA.

Russell Ouellette (R)

Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Massachusetts General Hospital, Boston, USA.

Leszek Stawiarz (L)

Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.

Jan Hillert (J)

Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.

Jason Talbott (J)

Department of Radiology and Biomedical Imaging, Zuckerberg San Francisco General Hospital, University of California, San Francisco, CA, USA.

Elise Bannier (E)

CHU Rennes, Radiology Department, Rennes, France.
Univ Rennes, CNRS, Inria, Inserm, IRISA UMR 6074, EMPENN - ERL U 1228, Rennes, France.

Anne Kerbrat (A)

Univ Rennes, CNRS, Inria, Inserm, IRISA UMR 6074, EMPENN - ERL U 1228, Rennes, France.
CHU Rennes, Neurology Department, Rennes, France.

Gilles Edan (G)

Univ Rennes, CNRS, Inria, Inserm, IRISA UMR 6074, EMPENN - ERL U 1228, Rennes, France.
CHU Rennes, Neurology Department, Rennes, France.

Pierre Labauge (P)

MS Unit, Department of Neurology, University Hospital of Montpellier, Montpellier, France.

Virginie Callot (V)

Aix Marseille University, CNRS, CRMBM, Marseille, France.
APHM, CHU Timone, CEMEREM, Marseille, France.

Jean Pelletier (J)

APHM, CHU Timone, CEMEREM, Marseille, France.
APHM, Department of Neurology, CHU Timone, APHM, Marseille.

Bertrand Audoin (B)

APHM, CHU Timone, CEMEREM, Marseille, France.
APHM, Department of Neurology, CHU Timone, APHM, Marseille.

Henitsoa Rasoanandrianina (H)

Aix Marseille University, CNRS, CRMBM, Marseille, France.
APHM, CHU Timone, CEMEREM, Marseille, France.

Jean-Christophe Brisset (JC)

Observatoire Français de la Sclérose en Plaques (OFSEP) ; Université de Lyon, Université Claude Bernard Lyon 1; Hospices Civils de Lyon; CREATIS-LRMN, UMR 5220 CNRS and U 1044 INSERM; Lyon, France.

Paola Valsasina (P)

Neuroimaging Research Unit, INSPE, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.

Maria A Rocca (MA)

Neuroimaging Research Unit, INSPE, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.

Massimo Filippi (M)

Neuroimaging Research Unit, INSPE, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.

Rohit Bakshi (R)

Brigham and Women's Hospital, Harvard Medical School, Boston, USA.

Shahamat Tauhid (S)

Brigham and Women's Hospital, Harvard Medical School, Boston, USA.

Ferran Prados (F)

Queen Square MS Centre, UCL Institute of Neurology, Faculty of Brain Sciences, University College London, London,UK.
Center for Medical Image Computing (CMIC), Department of Medical Physics and Biomedical Engineering, University College London, London, UK.

Marios Yiannakas (M)

Queen Square MS Centre, UCL Institute of Neurology, Faculty of Brain Sciences, University College London, London,UK.

Hugh Kearney (H)

Queen Square MS Centre, UCL Institute of Neurology, Faculty of Brain Sciences, University College London, London,UK.

Olga Ciccarelli (O)

Queen Square MS Centre, UCL Institute of Neurology, Faculty of Brain Sciences, University College London, London,UK.

Seth A Smith (SA)

Vanderbilt University Institute of Imaging Science, Vanderbilt University Medical Center, Nashville, TN, USA.

Constantina Andrada Treaba (C)

Massachusetts General Hospital, Boston, USA.

Caterina Mainero (C)

Massachusetts General Hospital, Boston, USA.

Jennifer Lefeuvre (J)

National Institute of Neurological Disorders and Stroke, National Institutes of Health, Maryland, USA.

Daniel S Reich (DS)

National Institute of Neurological Disorders and Stroke, National Institutes of Health, Maryland, USA.

Govind Nair (G)

National Institute of Neurological Disorders and Stroke, National Institutes of Health, Maryland, USA.

Timothy M Shepherd (TM)

Department of Radiology, NYU Langone Medical Center, New York, USA.

Erik Charlson (E)

Department of Radiology, NYU Langone Medical Center, New York, USA.

Yasuhiko Tachibana (Y)

National Institute of Radiological Sciences, Chiba, Chiba, Japan.

Masaaki Hori (M)

Department of Radiology, Juntendo University School of Medicine, Tokyo, Japan.

Kouhei Kamiya (K)

Department of Radiology, Juntendo University School of Medicine, Tokyo, Japan.

Lydia Chougar (L)

Department of Radiology, Juntendo University School of Medicine, Tokyo, Japan.
Hospital Cochin, Paris, France.

Sridar Narayanan (S)

McConnell Brain Imaging Centre, Montreal Neurological Institute, Montreal, Canada.

Julien Cohen-Adad (J)

NeuroPoly Lab, Institute of Biomedical Engineering, Polytechnique Montreal, Montreal, QC, Canada.
Department of Neuroscience, Faculty of Medicine, University of Montreal, Montreal, QC, Canada.
Functional Neuroimaging Unit, CRIUGM, Université de Montréal, Montreal, QC, Canada.

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