Application and a proposed modification of the 2010 McDonald criteria for the diagnosis of multiple sclerosis in a Canadian cohort of patients with clinically isolated syndromes
Abstract
Background The 2005 and 2010 McDonald criteria utilize magnetic resonance imaging (MRI) to provide evidence of disease dissemination in space (DIS) and time (DIT) for the diagnosis of multiple sclerosis (MS) in patients who have clinically isolated syndromes (CIS). Methods Data from 109 CIS patients not satisfying the 2005 criteria at entry into a randomized controlled minocycline trial were analyzed to determine the proportion who would have been diagnosed with MS at screening based on 2010 criteria. The impact of including symptomatic, as well as asymptomatic, MRI lesions to confirm DIT was also explored. Results Thirty percent (33/109) of patients, retrospectively, met the 2010 criteria for a diagnosis of MS at baseline. When both symptomatic and asymptomatic lesions were used to confirm DIT, three additional patients met the 2010 criteria. There was a significant 10.1% increase in the proportion of patients who met the 2010 DIS criteria, compared with the 2005 DIS criteria; however, two patients satisfied the 2005 DIS but not 2010 DIS criteria. Conclusion Using 2010 McDonald criteria, 30% of the CIS patients could be diagnosed with MS using a single MRI scan. Inclusion of symptomatic lesions in the DIT criteria further increases this proportion to 33%.
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Additional studies concerning the applicability of the 2010 McDonald Criteria in Asian, Middle Eastern, and Latin American populations have been published since 2010, though tended to be small.
“Additional studies concerning the applicability of the 2010 McDonald Criteria in Asian, 22-24 Middle Eastern, 25,26 and Latin American 27 populations have been published since 2010, though tended to be small.”
From Diagnosis of multiple sclerosis: 2017 revisions of the McDonald criteria (2018) · cites this paper as [22]
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Diagnosis of multiple sclerosis: 2017 revisions of the McDonald criteria
Thompson, A. J., Banwell, B. L., Barkhof, F., Carroll, W. M., Coetzee, T., Comi, G., Correale, J., Fazekas, F., Filippi, M., Freedman, M. S., et al. (2018) · The Lancet Neurology · doi:10.1016/s1474-4422(17)30470-2 · Cited by 8,167 · see citing works
Self-citation
- Authors
- Kang, H., Metz, L., Traboulsee, A., Eliasziw, M., Zhao, G., Cheng, Y., Zhao, Y., Li, D., the Minocycline in CIS Study Group, Traboulsee, A., Li, D., Riddehough, A., Cheng, Y., Lam, K., Lee, A., Zhao, G., Vorobeychik, G., Metz, L., Yeung, M., Yong, V., Hill, M., Cerchiaro, G., Ma, C., Topor, T., Blevins, G., Marriott, J., Kremenchutzky, M., Freedman, M., Lee, L., Duquette, P., Antel, J., Grand’Maison, F., Thibault, M., Bhan, V., & Eliasziw, M.
- Affiliations
- University of British Columbia (CA)
- University of Calgary (CA)
- Division of Neurology, Department of Medicine, University of British Columbia, Canada
- Tufts University (US)
- ORCID
- Venue
- Multiple Sclerosis Journal
- Publisher
- SAGE Publications
- Published
- 2013-08-22
- Volume
- 20
- Issue
- 4
- Pages
- 458-463
- ISSN
- 1352-4585 (ISSN-L)
- 1477-0970
- OpenAlex
- W2020947088
- Cited by
- 25
- References
- 0
- Citations by year
- 2025: 1 · 2024: 2 · 2022: 1 · 2021: 1 · 2020: 1 · 2019: 4 · 2018: 5 · 2017: 3 · 2016: 5 · 2015: 2
- FWCI
- 1.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Multiple Sclerosis Journal (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Multiple Sclerosis Society
- Topics
- Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
- Health Sciences › Medicine › Family Practice › Clinical Reasoning and Diagnostic Skills
- Health Sciences › Medicine › Oncology › Polyomavirus and related diseases
- Keywords
- multiple sclerosis diagnosis, clinically isolated syndrome, dissemination in space, dissemination in time, MRI lesions
- MeSH terms
- Adolescent, Adult, Canada, Demyelinating Diseases, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Minocycline, Multiple Sclerosis, Practice Guidelines as Topic, Disease Progression, Neuroprotective Agents, Young Adult
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