Evidence map›Paper›PMID 42307856›Full record

ArticleMolecular neurobiology2026

18:2 Cholesterol Ester is a Novel Prognostic Biomarker of Disease Progression in Multiple Sclerosis.

Pascual Torres, Anna Gil Sánchez, Agustín Sancho-Saldaña, Laura Quibus, Eduardo San Pedro Murillo, Emilio Ruiz-Fernández, Silvia Peralta, Maria José Solana, Luis Brieva, Cristina González-Mingot

Abstract read
In one paragraph

Article in Molecular neurobiology, 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
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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

10 authors.

Pascual TorresMetabolic Physiopathology Group, University of Lleida, IRBLleida, Av. Alcalde Rovira Roure, 80, 25198, Lleida, Spain. pascual.torres@udl.cat.
Anna Gil SánchezNeuroimmunology Group, Department of Medicine, University of Lleida, IRBLleida, Av. Alcalde Rovira Roure, 80, 25198, Lleida, Spain.
Agustín Sancho-SaldañaNeuroimmunology Group, Department of Medicine, University of Lleida, IRBLleida, Av. Alcalde Rovira Roure, 80, 25198, Lleida, Spain.
Laura QuibusNeuroimmunology Group, Department of Medicine, University of Lleida, IRBLleida, Av. Alcalde Rovira Roure, 80, 25198, Lleida, Spain.
Eduardo San Pedro MurilloDepartment of Neurology, Hospital Universitari Arnau de Vilanova, 25198, Lleida, Spain.
Emilio Ruiz-FernándezDepartment of Neurology, Hospital Universitari Arnau de Vilanova, 25198, Lleida, Spain.
Silvia PeraltaNeuroimmunology Group, Department of Medicine, University of Lleida, IRBLleida, Av. Alcalde Rovira Roure, 80, 25198, Lleida, Spain.
Maria José SolanaNeuroimmunology Group, Department of Medicine, University of Lleida, IRBLleida, Av. Alcalde Rovira Roure, 80, 25198, Lleida, Spain.
Luis BrievaNeuroimmunology Group, Department of Medicine, University of Lleida, IRBLleida, Av. Alcalde Rovira Roure, 80, 25198, Lleida, Spain. luis.brieva@udl.cat.
Cristina González-MingotNeuroimmunology Group, Department of Medicine, University of Lleida, IRBLleida, Av. Alcalde Rovira Roure, 80, 25198, Lleida, Spain. cristina.gonzalez@udl.cat.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) presents diverse clinical outcomes. Cholesterol esterification (CE) has been implicated as a disease mechanism involved in the remyelination process. We investigated whether cerebrospinal fluid (CSF) 18:2 cholesterol ester (18:2 CE) levels at diagnosis could predict 10-year MS progression. We aimed to determine if CSF 18:2 CE levels correlate with long-term disease progression. In a retrospective case-control single-centre study with 115 MS patients and 57 controls, we conducted targeted lipidomic analysis of CSF. Clinical data, oligoclonal bands, brain and spinal cord MRI, and CSF 18:2 CE levels were collected. Elevated CSF 18:2 CE levels were significantly associated with a higher risk of 10-year MS progression, with an AUC of 0.91 in a multivariable logistic regression model. Patients initially treated with a high-efficacy drug did not show a worse prognosis despite presenting elevated CE18:2 levels at the time of diagnosis. However, patients treated with a high-efficacy drug as a second or third option showed a positive correlation between CE18:2 levels and EDSS at 10 years. CSF 18:2 CE is a potential prognostic biomarker for predicting long-term MS progression, potentially indicating reduced remyelination capacity. These findings hold promise for improved patient management and warrant prospective validation.

Indexed as

Cholesterol EstersDisease ProgressionMultiple SclerosisAdultBiomarkersCase-Control StudiesFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesBiomarkersCholesterol EstersBiomarkersCholesterolDisease progressionLipidMultiple sclerosisPIRARetrospective study

Identifiers

PMID42307856
PMCPMC13275756

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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.