Evidence map›Paper›PMID 39277188›Full record

ArticleOpen heart2024

Intestinal fatty acid binding protein is associated with infarct size and cardiac function in acute heart failure following myocardial infarction.

Andraž Nendl, Geir Øystein Andersen, Ingebjørg Seljeflot, Marius Trøseid, Ayodeji Awoyemi

Abstract read
In one paragraph

Article in Open heart, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
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

5 authors.

Andraž NendlOslo Center for Clinical Heart Research, Department of Cardiology Ullevaal, Oslo University Hospital, Oslo, Norway andraz.nendl@medisin.uio.no.ORCID 0000-0003-2524-4389
Geir Øystein AndersenDepartment of Cardiology Ullevaal, Oslo University Hospital, Oslo, Norway.
Ingebjørg SeljeflotOslo Center for Clinical Heart Research, Department of Cardiology Ullevaal, Oslo University Hospital, Oslo, Norway.
Marius TrøseidInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
Ayodeji AwoyemiDepartment of Cardiology Ullevaal, Oslo University Hospital, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn acute heart failure (HF), reduced cardiac output, vasoconstriction and congestion may damage the intestinal mucosa and disrupt its barrier function. This could facilitate the leakage of bacterial products into circulation and contribute to inflammation and adverse cardiac remodelling. We aimed to investigate gut leakage markers and their associations with inflammation, infarct size and cardiac function.

methodsWe examined 61 ST-elevation myocardial infarction (STEMI) patients who developed acute HF within 48 hours of successful percutaneous coronary intervention (PCI). Serial blood samples were taken to measure lipopolysaccharide (LPS), LPS-binding protein (LBP), soluble cluster of differentiation 14 (sCD14) and intestinal fatty acid binding protein (I-FABP). Cumulative areas under the curve (AUCs) from baseline to day 5 were calculated. Serial echocardiography was performed to assess left ventricular ejection fraction (LVEF), global longitudinal strain (GLS) and wall motion score index (WMSI). Single-photon emission CT (SPECT) was performed at 6 weeks to determine infarct size and LVEF.

resultsI-FABP

conclusionsIn primary PCI-treated STEMI patients with acute HF, I-FABP, a marker of intestinal epithelial damage, was associated with larger infarct size and worse cardiac function after 6 weeks.

Indexed as

BiomarkersFatty Acid-Binding ProteinsHeart FailurePercutaneous Coronary InterventionST Elevation Myocardial InfarctionVentricular Function, LeftAcute DiseaseAcute-Phase ProteinsAgedCarrier ProteinsEchocardiographyFemaleHumansLipopolysaccharide-Binding ProteinLipopolysaccharide ReceptorsLipopolysaccharidesAcute-Phase ProteinsBiomarkersCarrier ProteinsCD14 protein, humanFABP2 protein, humanFatty Acid-Binding ProteinsLipopolysaccharide-Binding ProteinLipopolysaccharide ReceptorsLipopolysaccharidesMembrane GlycoproteinsBiomarkersHeart FailureInflammationMyocardial Infarction

Identifiers

PMID39277188
PMCPMC11404232

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.