Nonlesional diffusely abnormal appearing white matter in clinically isolated syndrome: Prevalence, association with clinical and MRI features, and risk for conversion to multiple sclerosis.


Journal

Journal of neuroimaging : official journal of the American Society of Neuroimaging
ISSN: 1552-6569
Titre abrégé: J Neuroimaging
Pays: United States
ID NLM: 9102705

Informations de publication

Date de publication:
09 2021
Historique:
revised: 26 05 2021
received: 19 04 2021
accepted: 28 05 2021
pubmed: 16 6 2021
medline: 27 10 2021
entrez: 15 6 2021
Statut: ppublish

Résumé

While diffusely abnormal white matter (DAWM) is a nonlesional MRI abnormality identified in ∼25% of patients with multiple sclerosis (MS), it has yet to be investigated in patients at an earlier disease stage, namely clinically isolated syndrome (CIS). The goals of this study were to (1) determine the prevalence of DAWM in patients with a CIS suggestive of MS, (2) evaluate the association between DAWM and demographic, clinical, and MRI features, and (3) evaluate the prognostic significance of DAWM on conversion from CIS to MS. One hundred and forty-two CIS participants were categorized into DAWM and non-DAWM groups at baseline and followed for up to 24 months or until MS diagnosis. The primary outcome was conversion to MS (2005 McDonald criteria) within 6 months. DAWM was present in 27.5% of participants, and was positively associated with brainstem symptom onset, receiving corticosteroids, dissemination in space, and T DAWM is present in a similar proportion of patients with CIS and clinically definite MS, and it is associated with increased risk of conversion to MS over 6 months.

Sections du résumé

BACKGROUND AND PURPOSE
While diffusely abnormal white matter (DAWM) is a nonlesional MRI abnormality identified in ∼25% of patients with multiple sclerosis (MS), it has yet to be investigated in patients at an earlier disease stage, namely clinically isolated syndrome (CIS). The goals of this study were to (1) determine the prevalence of DAWM in patients with a CIS suggestive of MS, (2) evaluate the association between DAWM and demographic, clinical, and MRI features, and (3) evaluate the prognostic significance of DAWM on conversion from CIS to MS.
METHODS
One hundred and forty-two CIS participants were categorized into DAWM and non-DAWM groups at baseline and followed for up to 24 months or until MS diagnosis. The primary outcome was conversion to MS (2005 McDonald criteria) within 6 months.
RESULTS
DAWM was present in 27.5% of participants, and was positively associated with brainstem symptom onset, receiving corticosteroids, dissemination in space, and T
CONCLUSIONS
DAWM is present in a similar proportion of patients with CIS and clinically definite MS, and it is associated with increased risk of conversion to MS over 6 months.

Identifiants

pubmed: 34128576
doi: 10.1111/jon.12900
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

981-994

Informations de copyright

© 2021 American Society of Neuroimaging.

Références

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Auteurs

R Davis Holmes (RD)

Department of Radiology, University of British Columbia, Vancouver, British Columbia, Canada.

Irene M Vavasour (IM)

Department of Radiology, University of British Columbia, Vancouver, British Columbia, Canada.

Jamie Greenfield (J)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

Guojun Zhao (G)

Department of Radiology, University of British Columbia, Vancouver, British Columbia, Canada.
UBC MS/MRI Research Group, University of British Columbia, Vancouver, British Columbia, Canada.

Jimmy S Lee (JS)

Department of Radiology, University of British Columbia, Vancouver, British Columbia, Canada.

G R Wayne Moore (GRW)

Department of Pathology & Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
International Collaboration on Repair Discoveries (ICORD), University of British Columbia, Vancouver, British Columbia, Canada.

Roger Tam (R)

Department of Radiology, University of British Columbia, Vancouver, British Columbia, Canada.
UBC MS/MRI Research Group, University of British Columbia, Vancouver, British Columbia, Canada.
School of Biomedical Engineering, University of British Columbia, Vancouver, British Columbia, Canada.

Luanne M Metz (LM)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

Anthony Trablousee (A)

UBC MS/MRI Research Group, University of British Columbia, Vancouver, British Columbia, Canada.
Department of Medicine (Neurology), University of British Columbia, Vancouver, British Columbia, Canada.

David K B Li (DKB)

Department of Radiology, University of British Columbia, Vancouver, British Columbia, Canada.
UBC MS/MRI Research Group, University of British Columbia, Vancouver, British Columbia, Canada.
Department of Medicine (Neurology), University of British Columbia, Vancouver, British Columbia, Canada.

Cornelia Laule (C)

Department of Radiology, University of British Columbia, Vancouver, British Columbia, Canada.
Department of Pathology & Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
International Collaboration on Repair Discoveries (ICORD), University of British Columbia, Vancouver, British Columbia, Canada.
Department of Physics & Astronomy, University of British Columbia, Vancouver, British Columbia, Canada.

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