Evidence map›Paper›PMID 39179712›Full record

ArticleJournal of neurology2024

Disability trajectories by progression independent of relapse activity status differ in pediatric, adult and late-onset multiple sclerosis.

Marta Simone, Giuseppe Lucisano, Tommaso Guerra, Damiano Paolicelli, Maria A Rocca, Vincenzo Brescia Morra, Francesco Patti, Pietro Annovazzi, Claudio Gasperini, Giovanna De Luca and 16 more

Abstract read
In one paragraph

Article in Journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–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

9 citing papers in PubMed.

  1. A multicentre, prospective, randomized, open-label pragmatic trial to compare the effectiveness and safety of interferon beta-1a and glatiramer-acetate in paediatric patients affected by Multiple Sclerosis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Trial
  2. Article
  3. Big data in multiple sclerosis.Current opinion in neurology · 2026
    Review
  4. Review
  5. Observational
  6. Review
  7. Review
  8. Review
  9. Article
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

26 authors.

Marta SimoneChild Neuropsychiatry Unit, Department of Precision and Regenerative Medicine, Jonic Area University of Bari "Aldo Moro", Bari, Italy.
Giuseppe LucisanoCORESEARCH, Pescara, Italy.
Tommaso GuerraDepartment of Translational Biomedicine and Neurosciences-DiBraiN, University "Aldo Moro" Bari, Piazza Giulio Cesare 11, 70124, Bari, Italy.
Damiano PaolicelliDepartment of Translational Biomedicine and Neurosciences-DiBraiN, University "Aldo Moro" Bari, Piazza Giulio Cesare 11, 70124, Bari, Italy.
Maria A RoccaDipartimento di Neurologia, Neurofisiologia e Neuroriabilitazione, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.
Vincenzo Brescia MorraDepartment of Neuroscience (NSRO), Multiple Sclerosis Clinical Care and Research Center, Federico II University, Naples, Italy.
Francesco PattiDipartimento di Scienze Mediche e Chirurgiche e Tecnologie Avanzate, GF Ingrassia, Sez. Neuroscienze, Centro Sclerosi Multipla, Università di Catania, Catania, Italy.
Pietro AnnovazziNeuroimmunology Unit - Multiple Sclerosis Centre ASST Valle Olona, Gallarate Hospital, Gallarate, Italy.
Claudio GasperiniDepartment of Neurosciences, S.Camillo Forlanini Hospital, Rome, Italy.
Giovanna De LucaCentro Sclerosi Multipla, Clinica Neurologica, Policlinico SS. Annunziata, Chieti, Italy.
Diana FerraroAzienda Ospedaliera Universitaria di Modena/OCB, UO Neurologia, Milano, Italy.
Lucia MargariChild Neuropsychiatry Unit, Department of Precision and Regenerative Medicine, Jonic Area University of Bari "Aldo Moro", Bari, Italy.
Franco GranellaUnit of Neurosciences, Department of Medicine and Surgery, University of Parma, Parma, Italy.
Carlo PozzilliDepartment of Human Neuroscience, Multiple Sclerosis Center, S. Andrea Hospital, Rome, Italy.
Silvia RomanoDepartment of Neurosciences, Mental Health and Sensory Organs, Centre for Experimental Neurological Therapies (CENTERS), Sapienza University of Rome, Rome, Italy.
Paola PeriniDepartment of Neurosciences, Multiple Sclerosis Centre-Veneto Region (CeSMuV), University Hospital of Padua, Padua, Italy.
Roberto BergamaschiIRCCS Mondino Foundation, Pavia, Italy.
Maria Gabriella ConiglioCenter for Multiple Sclerosis, Hospital ASM "Madonna delle Grazie", 75100, Matera, Italy.
Giacomo LusMultiple Sclerosis Center, II Division of Neurology, Department of Clinical and Experimental Medicine, Second University of Naples, Naples, Italy.
Marika VianelloUnit of Neurology, Cà Foncello Hospital, Treviso, Italy.
Alessandra LugaresiIRCCS Istituto Scienze Neurologiche di Bologna, Bologna, Italy.
Emilio PortaccioDepartment NEUROFARBA, University of Florence, Florence, Italy.
Massimo FilippiDipartimento di Neurologia, Neurofisiologia e Neuroriabilitazione, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.
Maria Pia AmatoDepartment NEUROFARBA, University of Florence, Florence, Italy.
Pietro IaffaldanoDepartment of Translational Biomedicine and Neurosciences-DiBraiN, University "Aldo Moro" Bari, Piazza Giulio Cesare 11, 70124, Bari, Italy. pietro.iaffaldano@uniba.it.ORCID http://orcid.org/0000-0003-2308-1731
Italian Multiple Sclerosis Register

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo compare Expanded Disability Status Scale (EDSS) trajectories over time between Multiple Sclerosis (MS) groups with pediatric (POMS), adult (AOMS) and late (LOMS) onset, and between patients with and without progression independent of relapse activity (PIRA).

methodsPatients with a first visit within 1 year from onset, ≥ 5-year follow-up and ≥ 1 visit every 6 months were selected from the Italian MS Register. Adjusted disability trajectories were assessed by longitudinal models for repeated measures. Comparisons between groups and between patients with and without PIRA in subgroups were performed by evaluating the yearly differences of mean EDSS score changes versus baseline (delta-EDSS). A first CDA event was defined as a 6-months confirmed disability increase from study baseline, measured by EDSS (increase ≥ 1.5 points with baseline EDSS = 0; ≥ 1.0 with baseline EDSS score ≤ 5.0 and ≥ 0.5 point with baseline EDSS > 5.5). PIRA was defined as a CDA event occurring more than 90 days after and more than 30 days before the onset of a relapse.

results3777 MS patients (268 POMS, 3282 AOMS, 227 LOMS) were included. The slope of disability trajectories significantly diverged in AOMS vs POMS starting from the second year of follow-up (Year 2: delta2-EDSS 0.18 (0.05; 0.31), p = 0.0054) and then mean delta2-EDSS gradually increased up to 0.23 (0.07; 0.39, p = 0.004) at year 5. Patients with PIRA had significant (p < 0.0001) steeper increase in EDSS scores than those without PIRA in all groups, although in POMS, the disability trajectories began to diverge later and at a lesser extent with delta-EDSS score of 0.48 vs 0.83 in AOMS and 1.57 in LOMS, at 3 years after the first PIRA.

conclusionsAge is relevant in determining disability progression in MS. POMS shows a less steep increase in EDSS scores over time than older patients. The effect of PIRA in accelerating EDSS progression is less pronounced in POMS than in AOMS and LOMS.

Indexed as

Age of OnsetDisability EvaluationDisease ProgressionMultiple SclerosisAdolescentAdultChildFemaleFollow-Up StudiesHumansItalyLongitudinal StudiesMaleMiddle AgedMultiple Sclerosis, Relapsing-RemittingRecurrenceAOMSDisability trajectoriesLOMSPIRAPOMS

Identifiers

PMID39179712
PMCPMC11447039

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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.