Evidence map›Paper›PMID 31383928›Full record

ArticleScientific reports2019

Lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis.

L Nogueras, H Gonzalo, M Jové, J Sol, A Gil-Sanchez, J V Hervás, P Valcheva, C Gonzalez-Mingot, M J Solana, S Peralta and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 61 citations in OpenAlex.

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  7. Metabolomics: a new frontier in neurodegenerative disease biomarker discovery.Metabolomics : Official journal of the Metabolomic Society · 2025
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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

12 authors at 3 institutions in 1 country.

L NoguerasUniversitat de Lleida (UdL), Lleida, Spain. lara.noguerasp@gmail.com.
H GonzaloInstitut de Recerca Biomèdica de Lleida (IRB-Lleida), Lleida, Spain.
M JovéUniversitat de Lleida (UdL), Lleida, Spain.
J SolUniversitat de Lleida (UdL), Lleida, Spain.
A Gil-SanchezInstitut de Recerca Biomèdica de Lleida (IRB-Lleida), Lleida, Spain.
J V HervásHospital Universitario Arnau de Vilanova Hospital (HUAV), Lleida, Spain.
P ValchevaInstitut de Recerca Biomèdica de Lleida (IRB-Lleida), Lleida, Spain.
C Gonzalez-MingotHospital Universitario Arnau de Vilanova Hospital (HUAV), Lleida, Spain.
M J SolanaHospital Universitario Arnau de Vilanova Hospital (HUAV), Lleida, Spain.
S PeraltaHospital Universitario Arnau de Vilanova Hospital (HUAV), Lleida, Spain.
R PamplonaUniversitat de Lleida (UdL), Lleida, Spain.
L BrievaHospital Universitario Arnau de Vilanova Hospital (HUAV), Lleida, Spain.
Hospital Universitari Arnau de Vilanova · ESBiomedical Research Institute of Lleida · ESUniversitat de Lleida · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is a complex multifactorial neuropathology. Although its etiology remains unclear, it has been demonstrated that the immune system attacks myelin, leading to demyelination and axonal damage. The involvement of lipids as one of the main components of myelin sheaths in MS and other demyelinating diseases has been postulated. However, it is still a matter of debate whether specific alteration patterns exist over the disease course. Here, using a lipidomic approach, we demonstrated that, at the time of diagnosis, the cerebrospinal fluid of MS patients presented differences in 155 lipid species, 47 of which were identified. An initial hierarchical clusterization was used to classify MS patients based on the presence of 25 lipids. When a supervised method was applied in order to refine this classification, a lipidomic signature was obtained. This signature was composed of 15 molecules belonging to five different lipid families including fatty acids (FAs). An FA-targeted approach revealed differences in two members of this family: 18:3n3 and 20:0 (arachidic acid). These results reveal a CSF lipidomic signature in MS patients at the time of diagnosis that might be considered as a potential diagnostic tool.

Indexed as

AdultDisease ProgressionFemaleHumansLipidomicsLipidsMaleMiddle AgedMultiple SclerosisLipids

Identifiers

PMID31383928
PMCPMC6683197
OpenAlexW2965647501

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.