Cited by 551Multiple Sclerosis Research StudiesPolyomavirus and related diseasesClinical Reasoning and Diagnostic Skills

Diagnosis of multiple sclerosis: 2024 revisions of the McDonald criteria

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Montalban, Xavier, Lebrun-Frénay, Christine, Oh, Jiwon, Arrambide, Georgina, Moccia, Marcello, Pia Amato, Maria, Amezcua, Lilyana, Banwell, Brenda +48 more·2025·The Lancet Neurology

Abstract

Advances in the understanding of multiple sclerosis and the development of biomarkers of pathophysiology prompted a substantial revision of the 2017 McDonald diagnostic criteria. The new 2024 McDonald criteria provide a unified approach for diagnosing multiple sclerosis in individuals with relapsing or progressive courses throughout the lifespan (ie, from paediatric to late-life presentations). The optic nerve can now serve as a fifth anatomical location within the CNS for diagnosis. The central vein sign, paramagnetic rim lesions, and kappa free-light chain concentrations in CSF can be used, when available, to provide supportive evidence and confer specificity for a diagnosis of multiple sclerosis in specific situations. In certain cases, radiologically isolated syndrome or neurological symptoms that do not constitute a clear attack or progression of disability can fulfil the criteria for a multiple sclerosis diagnosis. We also provide guidance for the diagnosis of multiple sclerosis in older individuals (≥50 years) and those with comorbidities. The 2024 revised criteria should expedite the diagnosis of multiple sclerosis, while maintaining specificity.

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Crossref · 10.1016/s1474-4422(25)00270-4

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  • In multiple sclerosis, the McDonald criteria are the standard criteria for disease diagnosis; according to these criteria, patients must present with multiple lesions in the central nervous system that are disseminated in space.

    “In MS, the McDonald criteria are the standard criteria for disease diagnosis. According to these criteria, patients must present with multiple lesions in the central nervous system (CNS) that are disseminated in space (Montalban et al. 2025).”

    From The Prevalence of Neuropathic Pain in Multiple Sclerosis—A Systematic Review and Meta‐Analysis Using the <scp>NeuPSIG</scp> Algorithm (2026) · cites this paper as Montalban et al. 2025

    The indexed title identifies the McDonald criteria as criteria for diagnosing multiple sclerosis. However, the available passages contain only title and citation metadata; they do not establish that the criteria are the standard or that patients must have multiple CNS lesions disseminated in space. Searches for dissemination in space and lesion locations found no passage stating those requirements. (LLM, conf=0.70)

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  • The 2024 revisions aim to increase diagnostic sensitivity while incorporating additional features intended to preserve, even increase, diagnostic specificity, thereby enabling an earlier and more accurate diagnosis of MS.

    “These revisions aim to increase diagnostic sensitivity while incorporating additional features intended to preserve, even increase, diagnostic specificity, thereby enabling an earlier and more accurate diagnosis of MS.8”

    From Applying the 2024-revised McDonald criteria for multiple sclerosis using conventional diagnostic tools: a single-centre prospective cohort study in Germany (2026) · cites this paper as [8]

    The indexed Abstract says the 2024 criteria should expedite MS diagnosis while maintaining specificity, and identifies additional features that can confer specificity in specific situations. It does not say that the revisions aim to increase specificity or explicitly claim increased diagnostic sensitivity or accuracy. (LLM, conf=0.83)

    Experimental — accuracy not yet measured
  • The 2024 revisions of the McDonald diagnostic criteria for multiple sclerosis include the optic nerve as a distinct fifth anatomical location for meeting dissemination in space criteria for relapsing- and progressive-onset MS.

    “The committee voted unanimously to include the optic nerve as a distinct, fifth anatomical location for meeting dissemination in space (DIS) criteria for relapsingand progressive-onset MS. 25”

    From The use of optical coherence tomography and visual evoked potentials in the 2024 McDonald diagnostic criteria for multiple sclerosis (2025) · cites this paper as [25]

    The indexed Abstract (page unavailable) says the 2024 criteria cover relapsing and progressive courses and that the optic nerve can serve as a fifth anatomical location for diagnosis. It does not state that the committee voted unanimously, as the citing sentence claims. (LLM, conf=0.83)

    Experimental — accuracy not yet measured
  • In the 2024 McDonald criteria for multiple sclerosis diagnosis, the optic nerve is added to the four previously designated dissemination-in-space regions (periventricular, juxtacortical/cortical, infratentorial, spinal cord), and dissemination-in-space criteria can be met with involvement of at least 2 of these 5 regions.

    “In the 2024 revisions of the McDonald criteria for diagnosis of multiple sclerosis, the optic nerve is added to the four previously designated DIS regions: peri-ventricular, juxta-cortical/cortical, infra-tentorial and spinal cord regions. DIS criteria for MS diagnosis can now be met with involvement of ≥ 2/5 of these regions (Panel 1). 25,26”

    From The use of optical coherence tomography and visual evoked potentials in the 2024 McDonald diagnostic criteria for multiple sclerosis (2025) · cites this paper as [25]

    Split into 2 atoms — 1 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 1 unverifiable. Expand the claim to see per-atom verdicts.

    Experimental — accuracy not yet measured
  • The optic nerve is incorporated as the fifth neuroanatomical topography for establishing DIS in the 2024-revised McDonald criteria.

    “The optic nerve is incorporated as the fifth neuroanatomical topography for establishing DIS, complementing periventricular, (juxta-)cortical, infratentorial, and spinal cord regions.8, 9, 10”

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Authors
Montalban, X., Lebrun-Frénay, C., Oh, J., Arrambide, G., Moccia, M., Pia Amato, M., Amezcua, L., Banwell, B., Bar-Or, A., Barkhof, F., Butzkueven, H., Ciccarelli, O., Chataway, J., Cohen, J. A., Comi, G., Correale, J., Deisenhammer, F., Filippi, M., Fiol, J., Freedman, M. S., Fujihara, K., Granziera, C., Green, A. J., Hartung, H.-P., Hellwig, K., Kappos, L., Kimbrough, D., Killestein, J., Lublin, F., Marignier, R., Ann Marrie, R., Miller, A., Otero-Romero, S., Ontaneda, D., Ramanathan, S., Reich, D., Rocca, M. A., Rovira, À., Saidha, S., Salter, A., Sastre-Garriga, J., Saylor, D., Solomon, A. J., Sormani, M. P., Stankoff, B., Tintore, M., Tremlett, H., Van der Walt, A., Viswanathan, S., Wiendl, H., Wildemann, B., Yamout, B., Zaratin, P., Calabresi, P. A., Coetzee, T., & Thompson, A. J.
Affiliations
  • St. Michael's Hospital (CA)
  • Universitat Autònoma de Barcelona (ES)
  • National Hospital for Neurology and Neurosurgery (GB)
  • University of Southern California (US)
  • Johns Hopkins University (US)
  • The Alfred Hospital (AU)
  • National Institute for Health and Care Research (GB)
  • Cleveland Clinic (US)
  • Vita-Salute San Raffaele University (IT)
  • Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia (AR)
  • Innsbruck Medical University (AT)
  • National Multiple Sclerosis Society (US)
  • University of Ottawa (CA)
  • Fukushima Medical University (JP)
  • University of Basel (CH)
  • University of California, San Francisco (US)
  • The University of Sydney (AU)
  • St. Josef-Hospital (DE)
  • Duke University (US)
  • Amsterdam University Medical Centers (NL)
  • Icahn School of Medicine at Mount Sinai (US)
  • Hospices Civils de Lyon (FR)
  • National Institutes of Health (US)
  • The University of Texas Southwestern Medical Center (US)
  • University of North Carolina at Chapel Hill (US)
  • University of Vermont (US)
  • University of Genoa (IT)
  • Sorbonne Université (FR)
  • University of British Columbia (CA)
  • Hospital Kuala Lumpur (MY)
  • University Hospital Heidelberg (DE)
  • University of Freiburg (DE)
Venue
The Lancet Neurology
Publisher
Elsevier BV
Published
2025-10
Volume
24
Issue
10
Pages
850-865
ISSN
1474-4422 (ISSN-L)
OpenAlex
W4414272694
Cited by
551
References
6
Citations by year
2026: 472 · 2025: 74 · 2024: 1 · 2019: 1
FWCI
84.91
Type
journal article
Language
en
Open access
Locations
  • The Lancet Neurology (publishedVersion)
  • PubMed (publishedVersion)
  • Pure Amsterdam UMC (publishedVersion, other-oa)
  • UCL Discovery (University College London) (submittedVersion)
  • FreiDok plus (Universitätsbibliothek Freiburg) (submittedVersion)
  • Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele (submittedVersion, cc-by-nc-nd)
  • CINECA IRIS Institutial Research Information System (University of Genoa) (submittedVersion)
Funders
  • European Committee for Treatment and Research in Multiple Sclerosis
  • National Multiple Sclerosis Society
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
  • Health Sciences › Medicine › Oncology › Polyomavirus and related diseases
  • Health Sciences › Medicine › Family Practice › Clinical Reasoning and Diagnostic Skills
Keywords
multiple sclerosis, McDonald criteria, diagnostic criteria revision, relapsing-remitting multiple sclerosis, secondary progressive multiple sclerosis, pediatric multiple sclerosis, optic nerve lesions, central vein sign, paramagnetic rim lesions, kappa free light chains, cerebrospinal fluid biomarkers, radiologically isolated syndrome, diagnostic specificity
MeSH terms
Humans, Magnetic Resonance Imaging, Multiple Sclerosis

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