Evidence map›Paper›PMID 26000321›Full record

ArticleAnnals of clinical and translational neurology2015

Predictors of disability worsening in clinically isolated syndrome.

Vilija G Jokubaitis, Tim Spelman, Tomas Kalincik, Guillermo Izquierdo, François Grand'Maison, Pierre Duquette, Marc Girard, Alessandra Lugaresi, Pierre Grammond, Raymond Hupperts and 26 more

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Review
  7. Article
  8. Article
  9. The Pharmacogenetics of Rituximab: Potential Implications for Anti-CD20 Therapies in Multiple Sclerosis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
    Review
  10. Aggressive multiple sclerosis (1): Towards a definition of the phenotype.Multiple sclerosis (Houndmills, Basingstoke, England) · 2020
    Article
  11. Does CSF pleocytosis have a predictive value for disease course in MS?Neurology(R) neuroimmunology & neuroinflammation · 2019
    Article
  12. Article
  13. Article
  14. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

36 authors.

Vilija G JokubaitisDepartment of Medicine (RMH), The University of Melbourne Parkville, Australia.
Tim SpelmanDepartment of Neurology, Royal Melbourne Hospital Parkville, Australia.
Tomas KalincikDepartment of Medicine (RMH), The University of Melbourne Parkville, Australia.
Guillermo IzquierdoHospital Universitario Virgen Macarena Sevilla, Spain.
François Grand'MaisonNeuro Rive-Sud, Hôpital Charles LeMoyne Quebec, Canada.
Pierre DuquetteHôpital Notre Dame Montreal, Canada.
Marc GirardHôpital Notre Dame Montreal, Canada.
Alessandra LugaresiMS Center, Department of Neuroscience and Imaging, University "G. d'Annunzio" Chieti, Italy.
Pierre GrammondCentre de réadaptation déficience physique Chaudière-Appalache Levis, Canada.
Raymond HuppertsOrbis Medical Centre Sittard, The Netherlands.
José Cabrera-GomezCIREN Havana, Cuba.
Celia Oreja-GuevaraUniversity Hospital San Carlos Madrid, Spain.
Cavit BozKaradeniz Technical University Trabzon, Turkey.
Giorgio GiulianiOspedale di Macerata Macerata, Italy.
Ricardo Fernández-BolañosHospital Universitario Virgen de Valme Seville, Spain.
Gerardo IulianoOspedali Riuniti di Salerno Salerno, Italy.
Jeannette Lechner-ScottJohn Hunter Hospital Newcastle, Australia.
Freek VerheulGroene Hart ziekenhuis Gouda, The Netherlands.
Vincent van PeschCliniques Universitaires Saint-Luc Brussels, Belgium.
Tatjana Petkovska-BoskovaJZU Clinic for Neurology Skopje, Republic of Macedonia.
Marcela FiolFLENI Buenos Aires, Argentina.
Fraser MooreJewish General Hospital Montreal, Canada.
Edgardo CristianoHospital Italiano Buenos Aires, Argentina.
Raed AlroughaniAmiri Hospital Kuwait City, Kuwait.
Roberto BergamaschiNeurological Institute IRCCS Mondino Pavia, Italy.
Michael BarnettBrain and Mind Research Institute Sydney, Australia.
Mark SleeFlinders University and Medical Centre Adelaide, Australia.
Norbert VellaMater Dei Hospital Msida, Malta.
Joseph HerbertNew York University Langone Medical Center New York, New York.
Cameron ShawGeelong Hospital Geelong, Australia.
Maria Laura SaladinoINEBA Buenos Aires, Argentina.
Maria Pia AmatoDepartment of Neurology University of Florence Florence, Italy.
Danny LiewMelbourne EpiCentre, University of Melbourne and Melbourne Health Melbourne, Australia.
Damiano PaolicelliDepartment of Basic Medical Sciences, Neuroscience and Sense Organs, University of Bari Bari, Italy.
Helmut ButzkuevenDepartment of Medicine (RMH), The University of Melbourne Parkville, Australia ; Department of Neurology, Royal Melbourne Hospital Parkville, Australia.
Maria TrojanoDepartment of Basic Medical Sciences, Neuroscience and Sense Organs, University of Bari Bari, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess demographic, clinical, magnetic resonance imaging, and treatment exposure predictors of time to 3 or 12-month confirmed disability worsening in clinically isolated syndrome (CIS) and early multiple sclerosis (MS).

methodsWe utilized the MSBase Incident Study (MSBasis), a prospective cohort study of outcome after CIS. Predictors of time to first 3 and 12-month confirmed expanded disability status scale worsening were analyzed using Cox proportional hazards regression.

resultsAbout 1989 patients were analyzed, the largest seen-from-onset cohort reported to-date. A total of 391 patients had a first 3-month confirmed disability worsening event, of which 307 were sustained for 12 months. Older age at CIS onset (adjusted hazard ratio: aHR 1.17, 95% 1.06, 1.30), pyramidal (aHR 1.45, 95% CI 1.13, 1.89) and ambulation (HR 1.60, 95% CI 1.09, 2.34) system dysfunction, annualized relapse rate (aHR 1.20, 95% CI 1.18, 1.22), and lower proportion of observation time on treatment were associated with 3-month confirmed worsening. Predictors of time to 12-month sustained worsening included pyramidal system dysfunction (Hazard ratio: aHR 1.38, 95% CI 1.05, 1.83), and older age at CIS onset (aHR 1.17, 95% CI 1.04, 1.31). Greater proportion of follow-up time exposed to treatment was associated with greater reductions in the rate of worsening.

interpretationThis study provides class IV evidence for a strong protective effect of disease-modifying treatment to reduce disability worsening events in patients with CIS and early MS, and confirms age and pyramidal dysfunction at onset as risk factors.

Identifiers

PMID26000321
PMCPMC4435703

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.