Cited by 65Multiple Sclerosis Research StudiesPolyomavirus and related diseasesInflammatory Bowel Disease

The DOI matches its Crossref record; the references it cites are not checked yet.

Association of Very Early Treatment Initiation With the Risk of Long-term Disability in Patients With a First Demyelinating Event

Open access
Cobo-Calvo, Alvaro, Tur, Carmen, Otero-Romero, Susana, Carbonell-Mirabent, Pere, Ruiz, Mariano, Pappolla, Agustin, Villacieros Alvarez, Javier, Vidal-Jordana, Angela, Arrambide, Georgina, Castilló, Joaquín, Galan, Ingrid, Rodríguez Barranco, Marta, Midaglia, Luciana Soledad, Nos, Carlos, Rodriguez Acevedo, Breogan, Zabalza de Torres, Ana, Mongay, Neus, Rio, Jordi, Comabella, Manuel, Auger, Cristina, Sastre-Garriga, Jaume, Rovira, Alex, Tintore, Mar, Montalban, Xavier·2023·Neurology

Abstract

BACKGROUND AND OBJECTIVES: Early treatment is associated with better long-term outcomes in patients with a first demyelinating event and early multiple sclerosis (MS). However, magnetic resonance (MR) findings are not usually integrated to construct propensity scores (PSs) when evaluating outcomes. We assessed the association of receiving very early treatment with the risk of long-term disability including an MR score (MRS) in patients with a first demyelinating event. METHODS: We included 580 patients with a first demyelinating event prospectively collected between 1994 and 2021, who received at least 1 disease-modifying drug (DMD). Patients were classified into tertiles according to the cohort's distribution of the time from the first demyelinating event to the first DMD: first tertile (FT) or very early treatment (6 months; n = 194), second tertile (6.1-16 months, n = 192), and third tertile (TT) (16.1 months, n = 194). A 5-point MRS was built according to the sum of the following indicators: ≥9 brain lesions (1 point); ≥1 infratentorial lesion (1 point); ≥1 spinal cord (SC) lesion (1 point); ≥1 contrast-enhancing (CE) brain lesion (1 point); and ≥1 CE SC lesion (1 point). PS based on covariates and the MRS was computed for each of the outcomes. Inverse PS-weighted Cox and linear regression models assessed the risk of different outcomes between tertile groups. Finally, to confirm the role of MR in treatment decision, we studied the time elapsed from the first demyelinating event to treatment initiation according to the MRS in all patients with radiologic available information, renamed as raw-MRS. RESULTS: Very early treatment decreased the risk of reaching Expanded Disability Status Scale 3.0 (hazard ratio [HR] 0.55, 95% CI 0.32-0.97), secondary progressive MS (HR 0.40, 95% CI 0.19-0.85), and sustained disease progression at 12 months after treatment initiation (HR 0.50, 95% CI 0.29-0.84), when compared with patients from the TT group. Patients from the FT group had a lower disability progression rate (β estimate -0.009, 95% CI -0.016 to -0.002) and a lower severe disability measured by the Patient-Determined Disease Step (β estimate -0.52, 95% CI -0.91 to -0.13) than the TT group. Finally, there was a 62.4% reduction in the median time between the first demyelinating event and the first-ever treatment initiation from patients displaying a raw-MRS 1 to patients with a raw-MRS 5. DISCUSSION: Using PS models with and without MRS, we showed that treatment initiation at very early stages is associated with a reduction in the risk of long-term disability accrual in patients with a first demyelinating event. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that earlier treatment of patients with MS presenting with a first demyelinating event is associated with improved clinical outcomes.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1212/wnl.0000000000207664

Cites

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

The citation lists haven’t been fetched yet

References 44 · Cited by 65

Research works printed but not linked: 43

  1. 10.1001/archneurol.2011.1426 · DOI
  2. 10.1016/s0140-6736(09)61259-9 · DOI
  3. 10.1177/1352458512469695 · DOI
  4. 10.1212/wnl.0000000000003078 · DOI
  5. 10.1136/jnnp-2016-314843 · DOI
  6. 10.1016/s1474-4422(11)70262-9 · DOI
  7. 10.1016/j.msard.2019.05.014 · DOI
  8. 10.1016/s1474-4422(14)70191-7 · DOI
  9. 10.1016/s1474-4422(14)70005-5 · DOI
  10. 10.1056/nejm200009283431301 · DOI
  11. 10.1016/s0140-6736(07)61194-5 · DOI
  12. 10.1002/ana.21757 · DOI
  13. 10.1016/j.clineuro.2013.09.024 · DOI
  14. 10.1136/jnnp-2018-318360 · DOI · Paper page
  15. 10.1002/ana.24682 · DOI
  16. 10.1016/s1474-4422(15)00018-6 · DOI
  17. 10.1177/1352458514546788 · DOI
  18. 10.1177/1352458516675039 · DOI
  19. 10.1177/13524585211010128 · DOI
  20. 10.1111/ene.13692 · DOI
  21. 10.1001/jama.2018.20588 · DOI
  22. 10.1177/1352458512449681 · DOI
  23. 10.1093/brain/awv105 · DOI · Paper page
  24. 10.1111/ene.15422 · DOI
  25. 10.1002/ana.24747 · DOI
  26. 10.1093/brain/awaa231 · DOI
  27. 10.1212/wnl.0000000000011242 · DOI
  28. 10.1212/wnl.0000000000013016 · DOI
  29. 10.1212/wnl.0000000000012726 · DOI · Paper page
  30. 10.1016/s1474-4422(21)00095-8 · DOI · Paper page
  31. 10.1002/sim.7084 · DOI · Paper page
  32. 10.1016/j.jacc.2016.10.060 · DOI
  33. 10.1186/1471-2377-13-37 · DOI
  34. 10.1016/j.msard.2022.103644 · DOI
  35. 10.1212/wnl.0b013e318258f744 · DOI
  36. 10.1177/1352458515599450 · DOI
  37. 10.1136/jnnp-2013-306222 · DOI
  38. 10.1177/1352458517751049 · DOI
  39. 10.1001/jamaneurol.2020.1568 · DOI
  40. 10.1093/brain/awac016 · DOI · Paper page
  41. 10.1212/wnl.0000000000010135 · DOI
  42. 10.1001/jamaneurol.2018.4905 · DOI
  43. 10.1016/s1474-4422(20)30067-3 · DOI

Metadata

Authors
Cobo-Calvo, A., Tur, C., Otero-Romero, S., Carbonell-Mirabent, P., Ruiz, M., Pappolla, A., Villacieros Alvarez, J., Vidal-Jordana, A., Arrambide, G., Castilló, J., Galan, I., Rodríguez Barranco, M., Midaglia, L. S., Nos, C., Rodriguez Acevedo, B., Zabalza de Torres, A., Mongay, N., Rio, J., Comabella, M., Auger, C., Sastre-Garriga, J., Rovira, A., Tintore, M., & Montalban, X.
Affiliations
  • From the Centre d'Esclerosi Múltiple de Catalunya (Cemcat) (A.C.-C., C.T., S.O.-R., P.C.-M., A.P., J.V.A., A.V.-J., G.A., J.C., I.G., M.R.B., L.S.M., C.N., B.R.A., A.Z.d.T., N.M., J.R., M.C., J.S.-G., M.T., X.M.), Hospital Universitari Vall d'Hebron, Universitat Autonoma de Barcelona; Department of Neurology (M.R.), Hospital Universitario Doce de Octubre, Madrid; and Section of Neuroradiology (C.A., A.R.), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Spain.
  • Universitat Autònoma de Barcelona (ES)
Venue
Neurology
Published
2023-09-26
Volume
101
Issue
13
Pages
e1280-e1292
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W4384820775
Cited by
65
References
44
Citations by year
2026: 19 · 2025: 24 · 2024: 17 · 2023: 5
FWCI
12.94
Type
journal article
Language
en
Open access
Locations
  • Neurology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Sanofi
  • Biogen
  • Teva Pharmaceutical Industries
  • Celgene
  • European Committee for Treatment and Research in Multiple Sclerosis
  • Mylan
  • Bayer HealthCare
  • Generalitat de Catalunya
  • Ministerio de Economía y Competitividad
  • Eisai
  • Ministerio de Ciencia e Innovación
  • Red Española de Esclerosis Múltiple
  • Genentech
  • Agència de Gestió d'Ajuts Universitaris i de Recerca
  • Instituto de Salud Carlos III (PI21/01860, JR19/00007, PI20/00800, PI19/01606)
  • European Regional Development Fund
Topics
  • Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
  • Health Sciences › Medicine › Oncology › Polyomavirus and related diseases
  • Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
Keywords
multiple sclerosis, first demyelinating event, disease-modifying drugs, long-term disability, Expanded Disability Status Scale, secondary progressive multiple sclerosis, disease progression, brain lesions, spinal cord lesions, contrast-enhancing lesions, treatment timing, propensity score weighting, treatment decision-making, relapse rate
MeSH terms
Brain, Humans, Magnetic Resonance Imaging, Multiple Sclerosis, Multiple Sclerosis, Chronic Progressive

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review