Evidence map›Paper›PMID 36388220›Full record

ArticleFrontiers in neurology2022

Oligoclonal M bands and cervical spinal cord lesions predict early secondary progressive multiple sclerosis.

Carmen Alcalá Vicente, Laura Lacruz, Francisco Gascón, Sara Carratalà, Carlos Quintanilla-Bordás, Maria T Sanz, María Carcelén-Gadea, Javier Mallada, Joan Carreres, Laura Gabaldón Torres and 8 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 37% of its field
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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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

18 authors at 6 institutions in 1 country.

Carmen Alcalá VicenteNeuroimmunology Unit, Polytechnic and University Hospital La Fe, Valencia, Spain.
Laura LacruzNeuroimmunology Unit, Polytechnic and University Hospital La Fe, Valencia, Spain.
Francisco GascónNeurology Service, Clinic University Hospital of València, Valencia, Spain.
Sara CarratalàNeuroimmunology Unit, Polytechnic and University Hospital La Fe, Valencia, Spain.
Carlos Quintanilla-BordásNeuroimmunology Unit, Polytechnic and University Hospital La Fe, Valencia, Spain.
Maria T SanzDidactics of Mathematics Department, University of València, Valencia, Spain.
María Carcelén-GadeaNeurology Service, General Hospital of València, Valencia, Spain.
Javier MalladaNeurology Service, General Hospital of Elda, Alicante, Spain.
Joan CarreresRadiology Service, Polytechnic and University Hospital La Fe, Valencia, Spain.
Laura Gabaldón TorresNeurology Service, San Francesc de Borja Hospital, Valencia, Spain.
Jose Andres DominguezNeurology Service, Clinic University Hospital of València, Valencia, Spain.
Emmanuel CañizaresNeurology Service, La Ribera Hospital, Valencia, Spain.
Sara Gil-PerotinNeuroimmunology Unit, Polytechnic and University Hospital La Fe, Valencia, Spain.
Laura CubasNeuroimmunology Unit, Polytechnic and University Hospital La Fe, Valencia, Spain.
Raquel Gasqué RubioNeuroimmunology Unit, Polytechnic and University Hospital La Fe, Valencia, Spain.
Jéssica Castillo-VillalbaNeuroimmunology Unit, Polytechnic and University Hospital La Fe, Valencia, Spain.
Francisco Carlos Pérez-MirallesNeuroimmunology Unit, Polytechnic and University Hospital La Fe, Valencia, Spain.
Bonaventura CasanovaNeuroimmunology Unit, Polytechnic and University Hospital La Fe, Valencia, Spain.
Hospital Universitari i Politècnic La Fe · ESHospital Clínico Universitario de Valencia · ESHospital de La Ribera · ESHospital General de Elda · ESHospital General Universitario De Valencia · ESUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To determine baseline cerebrospinal fluid and magnetic resonance imaging (MRI) variables at the onset of a clinically isolated syndrome (CIS) suggestive of multiple sclerosis (MS) that predict evolution to secondary progressive MS (SPMS). Methods: 276 CIS patients with a minimum follow-up of 10 years were studied. Baseline presence of oligoclonal IgG and IgM bands (OCGB and OCMB respectively); number of brain T2 lesions (B-T2L), brain gadolinium enhancement lesions (brain-GEL), cervical spinal cord T2 lesions (cSC-T2L); and fulfillment of 2017 McDonald criteria among other variables were collected. Results: 14 patients ended up with a non-MS condition. 138/276 CIS patients fulfilled 2017 McDonald criteria. Mean age was 32.4 years, 185 female. 227 received treatment, 95 as CIS. After a mean follow-up of 12 years, 36 patients developed SPMS. Conversion to SPMS was associated with OCGB (p = 0.02), OCMB (p = 0.0001); ≥ 9 B-T2L (p = 0.03), brain-GEL (p = 0.03), and cSC-T2L (p = 0.03). However, after adjusting for sex, age, BT2L, brain-GEL, SC-T2, and OCMB status, only OCMB (HR 4.4, 1.9-10.6) and cSC-T2L (HR 2.2, 1.0-6.2) suggested an independent association with risk of conversion to SPMS. Patients with both risk factors had a HR of 6.12 (2.8-12.9). Discussion: OCMB and SC-T2 lesions are potential independent predictors of conversion to SPMS.

Indexed as

multiple sclerosisOCMBoligoclonal M bandssecondary progressive MSspinal cord

Identifiers

PMID36388220
PMCPMC9650197
OpenAlexW4307702129

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.