Evidence map›Paper›PMID 41609134›Full record

ReviewRevista de neurologia2026

[XVII Post-ECTRIMS Meeting: Review of the New Developments Presented at the 2024 ECTRIMS Congress (I)].

Óscar Fernández, Adrián Arés, Eduardo Agüera, Yolanda Aladro, Ana Alonso, Rafael Arroyo, Luis Brieva, Carmen Calles, Ana Belén Caminero, Tamara Castillo-Triviño and 14 more

Abstract readReviewEnglish Abstract
In one paragraph

Review in Revista de neurologia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

24 authors.

Óscar FernándezDepartamento de Farmacología, Facultad de Medicina, Instituto de Investigación Biomédica de Málaga (IBIMA), Hospital Universitario Regional de Málaga, Universidad de Málaga, 29010 Málaga, España.
Adrián ArésDepartamento de Neurología, Complejo Asistencial Universitario de León, 24008 León, España.
Eduardo AgüeraServicio de Neurología, Hospital Reina Sofía, 14004 Córdoba, España.
Yolanda AladroServicio de Neurología, Hospital Universitario de Getafe, 28905 Madrid, España.
Ana AlonsoUnidad de Esclerosis Múltiple, Servicio de Neurología, Hospital Regional Universitario de Málaga, 29010 Málaga, España.
Rafael ArroyoServicio de Neurología, Hospital Universitario Quirónsalud, 28223 Madrid, España.
Luis BrievaDepartamento de Medicina, Universitat de Lleida, Hospital Universitari Arnau de Vilanova, 25198 Lleida, España.
Carmen CallesServicio de Neurología, Hospital Universitario Son Espases, 07120 Palma de Mallorca, España.
Ana Belén CamineroDepartamento de Neurología, Complejo Asistencial de Ávila, 05071 Ávila, España.
Tamara Castillo-TriviñoServicio de Neurología, Hospital Universitario Donostia, Grupo de Neuroinmunología, IIS Biogipuzkoa, 20014 Donostia, España.
Lucienne Costa-FrossardCSUR de Esclerosis Múltiple, Hospital Ramón y Cajal, 28034 Madrid, España.
Sara EichauServicio de Neurología, Hospital Universitario Virgen Macarena, 41009 Sevilla, España.
Miguel Ángel HernándezServicio de Neurología, Hospital Nuestra Señora de Candelaria, 38010 Santa Cruz de Tenerife, España.
Lamberto LandeteServicio de Neurología, Hospital Universitario Doctor Peset, 46017 Valencia, España.
Miguel LlanezaServicio de Neurología, Hospital Universitario Central de Asturias, 33011 Oviedo, España.
Sara LlufriuUnidad de Neuroinmunología y Esclerosis Múltiple, Hospital Clínic de Barcelona e IDIBAPS, 08036 Barcelona, España.
José E Meca-LallanaUnidad de Neuroinmunología Clínica y CSUR Esclerosis Múltiple, Servicio de Neurología, Hospital Clínico Universitario Virgen de la Arrixaca (IMIB-Arrixaca), Cátedra de Neuroinmunología Clínica y Esclerosis Múltiple, Universidad Católica San Antonio (UCAM), 30120 Murcia, España.
Virginia Meca-LallanaServicio de Neurología, Hospital Universitario de la Princesa, 28006 Madrid, España.
Ester MoralServicio de Neurología, Complejo Hospitalario Universitario Moisès Broggi, 08970 Barcelona, España.
Celia Oreja-GuevaraServicio de Neurología, Hospital Clínico San Carlos, IdISSC; Departamento de Medicina, Facultad de Medicina, Universidad Complutense de Madrid (UCM), 28040 Madrid, España.
José María PrietoServicio de Neurología, Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), 15706 Santiago de Compostela, España.
Lucía Romero-PinelDepartamento de Neurologia, Hospital Universitari de Bellvitge-IDIBELL, 08908 L'Hospitalet de Llobregat, España.
Andreu VilasecaServei de Neurologia, Hospital Universitario Vall d'Hebron, CEMCAT, 08035 Barcelona, España.
Alfredo Rodríguez-AntigüedadServicio de Neurología, Hospital Universitario Cruces, 48903 Barakaldo, España.

Funding

Merck
6 · The paper itself

Abstract

introductionThe XVII edition of the post-European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) meeting was held on 4-5 October 2024 in Madrid. This event was attended by Spanish neurologists specialized in multiple sclerosis (MS), who presented a summary of the most relevant advances discussed at the ECTRIMS congress, held days before in Copenhagen.

aimTo present new developments in neurodegeneration and progression, the prodromal phase and diagnosis, the clinical use of biomarkers and neuroimaging, as well as the current role of patient-reported outcomes and digital monitoring. Highlights on the risk of infections and comorbidities in MS are also summarized. Content and Conclusions: In active MS lesions, there is no correlation between the myeloid cell phenotype and remyelination, while memory astrocytes, regulated by the CLEC16A gene, are present in chronic active lesions. Gray matter atrophy is associated with disability and progression independent of relapses, whereas cervical spinal cord atrophy predicts the prognosis of progressive forms and may lead to earlier diagnosis. Healthcare resource utilization increases in the years preceding the first demyelinating event, and although prodromal symptoms are highly variable, they are useful in identifying risk factors for the disease. The new McDonald criteria will facilitate the diagnosis of MS in patients with a radiologically isolated syndrome. Glial fibrillary acidic protein complements neurofilaments, and both biomarkers could soon be standardized for use in clinical practice; paramagnetic rim lesions and slowly expanding lesions are promising imaging markers. In another area, patient-reported health outcomes are valuable, although they are subject to selection bias and the need to define boundaries for their use. Finally, the risk of infections increases before diagnosis and may worsen with certain treatments. Comorbidities in MS should be managed as an integral part of disease management.

Indexed as

Multiple SclerosisBiomarkersCongresses as TopicDisease ProgressionHumansBiomarkersECTRIMSmultiple sclerosispost-ECTRIMS

Identifiers

PMID41609134
PMCPMC12873698

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.