Evidence map›Paper›PMID 40281287›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2025

Coronary artery disease is associated with particular change of serum metabolome: a case-control study.

Marcin Kondraciuk, Małgorzata Chlabicz, Jacek Jamiołkowski, Natalia Zieleniewska, Michał Ciborowski, Adrian Godlewski, Emilia Sawicka-Śmiarowska, Katarzyna Ptaszyńska, Magda Łapińska, Adam Krętowski and 1 more

Abstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Marcin KondraciukPopulation Research Centre, Medical University of Bialystok, Bialystok, Poland.
Małgorzata ChlabiczPopulation Research Centre, Medical University of Bialystok, Bialystok, Poland. mchlabicz@op.pl.
Jacek JamiołkowskiPopulation Research Centre, Medical University of Bialystok, Bialystok, Poland.
Natalia ZieleniewskaDepartment of Population Medicine and Lifestyle Diseases Prevention, Medical University of Bialystok, Bialystok, Poland.
Michał CiborowskiMetabolomics and Proteomics Laboratory, Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.
Adrian GodlewskiMetabolomics and Proteomics Laboratory, Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.
Emilia Sawicka-ŚmiarowskaDepartment of Cardiology, Medical University of Bialystok, Bialystok, Poland.
Katarzyna PtaszyńskaDepartment of Cardiology, Medical University of Bialystok, Bialystok, Poland.
Magda ŁapińskaDepartment of Population Medicine and Lifestyle Diseases Prevention, Medical University of Bialystok, Bialystok, Poland.
Adam KrętowskiMetabolomics and Proteomics Laboratory, Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.
Karol A KamińskiPopulation Research Centre, Medical University of Bialystok, Bialystok, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCardiovascular disease (CVD) is a significant cause of mortality worldwide. Preventive programs are trying to reduce the burden of the disease. Recent advances in metabolomics profiling open a new avenue for developing complementary CVD evaluation strategies.

objectivesThe aim of the study was to investigate whether a metabolomic profile can provide an additional characterisation of individuals with coronary artery disease (CAD).

methodsThe study included 167 participants with CAD aged 41-79 years. A control group was formed of 166 individuals without CAD, gender- and age-matched to the study group. A total of 188 metabolites were profiled in serum by liquid chromatography-tandem mass spectrometry. After clearing the data, associations between 132 metabolites and CAD presence were analysed using multiple linear regression models.

resultsWe observed significant differences in serum metabolic profiles between analysed groups on various levels. However, a deeper analysis revealed sphingomyelin 41:1 (SM 41:1) as the main metabolite independently associated with CAD after correction for classical CV risk factors. Its concentration was lower in the CAD group (median 9.79 µmol/L, interquartile range (IQR) 7.92-12.23) compared to control one (median 13.60 µmol/L, IQR 11.30-16.15) (p < 0.001). Further analysis showed that SM 41:1 concentration was inversely correlated with CAD, current smoking, and hypertension; and positively associated with female gender and non-HDL level.

conclusionsCAD patients present lower plasma concentrations of SM 41:1 than healthy subjects. A better understanding of the biological function of sphingomyelin in CAD patients may help develop therapeutic approaches and risk stratification in this group.

Indexed as

Coronary Artery DiseaseMetabolomeAdultAgedBiomarkersCase-Control StudiesChromatography, LiquidFemaleHumansMaleMetabolomicsMiddle AgedRisk FactorsSphingomyelinsTandem Mass SpectrometryBiomarkersSphingomyelinsCardiovascular diseaseCoronary artery diseaseMetabolomicsPrincipal component analysisSphingomyelin 41:1

Identifiers

PMID40281287
PMCPMC12031763

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.