Evidence map›Paper›PMID 37700226›Full record

ArticleBMC cardiovascular disorders2023

Analysis of circulating ceramides and hexosylceramides in patients with coronary artery disease and type II diabetes mellitus.

Philip Düsing, Nadine N Heinrich, Baravan Al-Kassou, Katharina Gutbrod, Peter Dörmann, Georg Nickenig, Felix Jansen, Andreas Zietzer

Open access · goldAbstract read
In one paragraph

Article in BMC cardiovascular disorders, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  10. The Circulating Lipidome In Severe Obesity.medRxiv : the preprint server for health sciences · 2025
    Article
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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

8 authors at 2 institutions in 1 country.

Philip DüsingHeart Center, Department of Internal Medicine II, University Hospital Bonn, Bonn, Germany.
Nadine N HeinrichHeart Center, Department of Internal Medicine II, University Hospital Bonn, Bonn, Germany.
Baravan Al-KassouHeart Center, Department of Internal Medicine II, University Hospital Bonn, Bonn, Germany.
Katharina GutbrodInstitute of Molecular Physiology and Biotechnology of Plants, University of Bonn, Bonn, Germany.
Peter DörmannInstitute of Molecular Physiology and Biotechnology of Plants, University of Bonn, Bonn, Germany.
Georg NickenigHeart Center, Department of Internal Medicine II, University Hospital Bonn, Bonn, Germany.
Felix JansenHeart Center, Department of Internal Medicine II, University Hospital Bonn, Bonn, Germany.
Andreas ZietzerHeart Center, Department of Internal Medicine II, University Hospital Bonn, Bonn, Germany. andreas.zietzer@ukbonn.de.
University Hospital Bonn · DEUniversity of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiovascular disease (CVD) remains the leading cause of death worldwide. The main driving force behind this association is coronary artery disease (CAD), the manifestation of atherosclerosis in the coronary circulation. Cornerstones in the development of CAD are pathologies in lipid metabolism. In recent years, ongoing research has identified ceramides, a subclass of sphingolipids to be mediators of CVD. The aim of this study is to investigate the influence of type II diabetes mellitus (DM) on circulating ceramides and hexosylceramides (HexCers) in CAD patients.

methods24 patients aged 40-90 years with CAD confirmed by angiography were included into a pilot study. Patients with DM were identified by analysis of discharge letters or other medical documents available at the study center. During coronary angiography, arterial blood samples were collected and quantification of sphingolipids in patient serum was performed by mass spectrometry.

resultsStatistical analysis showed nine significantly different HexCers in CAD patients with DM compared to patients without DM. Among the nine significantly regulated HexCers, we identified seven d18:1 HexCers. This group contributes to the fourth most abundant subgroup of total ceramides and HexCers in this dataset. HexCer-d18:1-23:1(2-OH) showed the strongest downregulation in the patient group with DM.

conclusionThis study suggests that levels of circulating HexCers are downregulated in patients with CAD and concomitant DM compared to patients without DM. Further research is needed to investigate the underlying mechanisms and the suitability of HexCers as possible mediators and/or prognostic markers in CAD.

Indexed as

Cardiovascular DiseasesCoronary Artery DiseaseDiabetes Mellitus, Type 2CeramidesCoronary AngiographyHumansPilot ProjectsSphingolipidsCeramidesSphingolipidsCeramidesCoronary artery diseaseDiabetes mellitus

Identifiers

PMID37700226
PMCPMC10498560
OpenAlexW4386647319

What OpenQuestion holds

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LicenceCC BY
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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.