Evidence map›Paper›PMID 40379482›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2025

Plasma CHI3L1 associates with brain volume loss and glial activation in multiple sclerosis.

Venla Ahola, Maija Saraste, Marjo Nylund, Markus Matilainen, Amelie Luoma, Anna Vuorimaa, Jussi Lehto, Sini Laaksonen, Eeva-Christine Brockmann, Jens Kuhle and 4 more

Abstract read
In one paragraph

Article in Journal of neurology, neurosurgery, and psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

  1. Pooled it
  2. Article
  3. Article
  4. 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

14 authors.

Venla AholaClinical Neurosciences, University of Turku, Turku, Finland.ORCID http://orcid.org/0009-0008-5615-5438
Maija SarasteClinical Neurosciences, University of Turku, Turku, Finland maija.saraste@utu.fi.ORCID http://orcid.org/0000-0002-3424-5976
Marjo NylundClinical Neurosciences, University of Turku, Turku, Finland.ORCID http://orcid.org/0000-0001-6695-5684
Markus MatilainenClinical Neurosciences, University of Turku, Turku, Finland.ORCID http://orcid.org/0000-0002-5597-2670
Amelie LuomaClinical Neurosciences, University of Turku, Turku, Finland.ORCID http://orcid.org/0009-0001-5689-052X
Anna VuorimaaClinical Neurosciences, University of Turku, Turku, Finland.ORCID http://orcid.org/0000-0002-0711-6917
Jussi LehtoTurku PET Centre, University of Turku, Turku University Hospital, and Åbo Akademi University, Turku, Finland.ORCID http://orcid.org/0000-0002-2589-2549
Sini LaaksonenClinical Neurosciences, University of Turku, Turku, Finland.ORCID http://orcid.org/0000-0002-1273-8630
Eeva-Christine BrockmannDepartment of Life Technologies, Division of Biotechnology, University of Turku, Turku, Finland.ORCID http://orcid.org/0009-0005-0362-0402
Jens KuhleDepartment of Neurology, University Hospital and University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0002-6963-8892
David LeppertDepartment of Neurology, University Hospital and University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0001-6172-801X
Tero SoukkaInFLAMES Research Flagship, University of Turku, Turku, Finland.ORCID http://orcid.org/0000-0002-1144-6724
Urpo LamminmäkiInFLAMES Research Flagship, University of Turku, Turku, Finland.ORCID http://orcid.org/0000-0002-6336-1407
Laura AirasClinical Neurosciences, University of Turku, Turku, Finland.ORCID http://orcid.org/0000-0002-9751-5881

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiple sclerosis (MS) progression independent of relapses is driven by brain innate immune cell activation. The aim of this study was to evaluate the association between chitinase-3-like protein 1 (CHI3L1), expressed in brain by astrocytes and microglia, measured from blood and smouldering inflammation measured using 18 kDa translocator protein (TSPO) positron emission tomography (PET) in patients with MS.

methodsThe study cohort included 55 patients with MS (25 progressive MS (PMS) and 30 relapsing remitting MS (RRMS)) and 17 healthy controls (HC). CHI3L1 was measured with commercial ELISA from plasma samples. A subcohort (44 MS and 9 HC) underwent TSPO-PET to assess [

resultsCHI3L1 concentration in plasma was higher in PMS (23.5 ng/mL) compared with HC (16.8 ng/mL, p=0.0055) and RRMS (19.3 ng/mL, p=0.049). CHI3L1 associated with brain [

conclusionsAssociation of CHI3L1 with glial activation and brain volume loss identifies plasma CHI3L1 as a promising biomarker for smouldering inflammation and MS progression-related pathology.

Indexed as

BrainChitinase-3-Like Protein 1Multiple SclerosisMultiple Sclerosis, Chronic ProgressiveMultiple Sclerosis, Relapsing-RemittingNeurogliaAdultFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedOrgan SizePositron-Emission TomographyCHI3L1 protein, humanChitinase-3-Like Protein 1MRIMULTIPLE SCLEROSISNEUROIMMUNOLOGYPET

Identifiers

PMID40379482
PMCPMC12573333

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.