Evidence map›Paper›PMID 26234719›Full record

ArticleAntioxidants & redox signaling2015

Interaction of MIF Family Proteins in Myocardial Ischemia/Reperfusion Damage and Their Influence on Clinical Outcome of Cardiac Surgery Patients.

Christian Stoppe, Steffen Rex, Andreas Goetzenich, Sandra Kraemer, Christoph Emontzpohl, Josefin Soppert, Luisa Averdunk, Yu Sun, Rolf Rossaint, Hongqi Lue and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Antioxidants & redox signaling, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 63 citations in OpenAlex.

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  8. Effect of macrophage migration inhibitory factor on pulmonary vein arrhythmogenesis through late sodium current.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2023
    Article
  9. Observational
  10. The role of CD74 in cardiovascular disease.Frontiers in cardiovascular medicine · 2022
    Review
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  13. TheJournal of clinical medicine · 2020
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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

19 authors at 7 institutions in 4 countries.

Christian Stoppe1 Institute of Biochemistry and Molecular Cell Biology, RWTH Aachen University , Aachen, Germany .
Steffen Rex3 Department of Anesthesiology, University Hospitals Leuven , Leuven, Belgium .
Andreas Goetzenich5 Department of Thoracic, Cardiac and Vascular Surgery, University Hospital, RWTH Aachen University , Aachen, Germany .
Sandra Kraemer1 Institute of Biochemistry and Molecular Cell Biology, RWTH Aachen University , Aachen, Germany .
Christoph Emontzpohl1 Institute of Biochemistry and Molecular Cell Biology, RWTH Aachen University , Aachen, Germany .
Josefin Soppert1 Institute of Biochemistry and Molecular Cell Biology, RWTH Aachen University , Aachen, Germany .
Luisa Averdunk1 Institute of Biochemistry and Molecular Cell Biology, RWTH Aachen University , Aachen, Germany .
Yu Sun1 Institute of Biochemistry and Molecular Cell Biology, RWTH Aachen University , Aachen, Germany .
Rolf Rossaint2 Department of Anesthesiology, University Hospital, RWTH Aachen University , Aachen, Germany .
Hongqi Lue1 Institute of Biochemistry and Molecular Cell Biology, RWTH Aachen University , Aachen, Germany .
Caleb Huang7 Department of Medicine, Yale University School of Medicine , New Haven, Connecticut.
Yan Song7 Department of Medicine, Yale University School of Medicine , New Haven, Connecticut.
Georgios Pantouris8 Department of Pharmacology, Yale University School of Medicine , New Haven, Connecticut.
Elias Lolis8 Department of Pharmacology, Yale University School of Medicine , New Haven, Connecticut.
Lin Leng7 Department of Medicine, Yale University School of Medicine , New Haven, Connecticut.
Wibke Schulte7 Department of Medicine, Yale University School of Medicine , New Haven, Connecticut.
Richard Bucala7 Department of Medicine, Yale University School of Medicine , New Haven, Connecticut.
Christian Weber9 Institute for Cardiovascular Prevention, Ludwig-Maximilians-University Munich , Munich, Germany .
Jürgen Bernhagen1 Institute of Biochemistry and Molecular Cell Biology, RWTH Aachen University , Aachen, Germany .
Yale University · USRWTH Aachen University · DEUniversitätsklinikum Aachen · DEGerman Centre for Cardiovascular Research · DEKU Leuven · BEMunich Cluster for Systems Neurology · DESecond Military Medical University · CN

Funding

MIF AND THE HOST RESPONSE TO INFECTIONR01AI042310 · NIAID · YALE UNIVERSITY · PI BUCALA, RICHARD J · 1998 to 2013
$4.3M
NIAID NIH HHS R01-AI42310
6 · The paper itself

Abstract

aimsCardiac surgery involves myocardial ischemia/reperfusion (I/R) with potentially deleterious consequences. Macrophage migration inhibitory factor (MIF) is a stress-regulating chemokine-like cytokine that protects against I/R damage, but functional links with its homolog, d-dopachrome tautomerase (MIF-2), and the circulating soluble receptor CD74 (sCD74) are unknown. In this study, we investigate the role of MIF, MIF-2, sCD74, and MIF genotypes in patients scheduled for elective single or complex surgical procedures such as coronary artery bypass grafting or valve replacement.

resultsMIF and MIF-2 levels significantly increased intraoperatively, whereas measured sCD74 decreased correspondingly. Circulating sCD74/MIF complexes were detectable in 50% of patients and enhanced MIF antioxidant activity. Intraoperative MIF levels were independently associated with a reduced risk for the development of atrial fibrillation (AF) (odds ratio 0.99 [0.98-1.00]; p=0.007). Circulating levels of MIF-2, but not MIF, were associated with an increased frequency of organ dysfunction and predicted the occurrence of AF (area under the curve [AUC]=0.663; p=0.041) and pneumonia (AUC=0.708; p=0.040). Patients with a high-expression MIF genotype exhibited a reduced incidence of organ dysfunction compared with patients with low-expression MIF genotypes (3 vs. 25; p=0.042). INNOVATION: The current study comprehensively highlights the kinetics and clinical relevance of MIF family proteins and the MIF genotype in cardiac surgery patients.

conclusionOur findings suggest that increased MIF levels during cardiac surgery feature organ-protective properties during myocardial I/R, while the soluble MIF receptor, sCD74, may enhance MIF antioxidant activity. In contrast, high MIF-2 levels are predictive of the development of organ dysfunction. Importantly, we provide first evidence for a gene-phenotype relationship between variant MIF alleles and clinical outcome in cardiac surgery patients.

Indexed as

AgedAnimalsAntigens, Differentiation, B-LymphocyteBiomarkersCell MovementCells, CulturedCoronary Artery BypassFemaleHistocompatibility Antigens Class IIHumansIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMaleMiddle AgedMyocardial Reperfusion InjuryNeutrophilsAntigens, Differentiation, B-LymphocyteBiomarkersdopachrome isomeraseHistocompatibility Antigens Class IIIntramolecular Oxidoreductasesinvariant chainMacrophage Migration-Inhibitory FactorsMIF protein, human

Identifiers

PMID26234719
PMCPMC4615780
OpenAlexW2423947669

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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.