Evidence map›Paper›PMID 32384583›Full record

ReviewJournal of cellular and molecular medicine2020

Cardiac metabolism as a driver and therapeutic target of myocardial infarction.

Coert J Zuurbier, Luc Bertrand, Christoph R Beauloye, Ioanna Andreadou, Marisol Ruiz-Meana, Nichlas R Jespersen, Duvaraka Kula-Alwar, Hiran A Prag, Hans Eric Botker, Maija Dambrova and 5 more

Open access · goldAbstract readReview
In one paragraph

Review in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed, 1 pooled it
13.0field-weighted citation impact, top 1% 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

137 citing papers in PubMed, 1 synthesis or guideline pooled it, 228 citations in OpenAlex.

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77 more citing papers are in PubMed but not listed here.

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

15 authors at 11 institutions in 10 countries.

Coert J ZuurbierDepartment of Anesthesiology, Laboratory of Experimental Intensive Care and Anesthesiology, Amsterdam Infection & Immunity, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Luc BertrandInstitut de Recherche Expérimentale et Clinique, Pole of Cardiovascular Research, Université catholique de Louvain, Brussels, Belgium.
Christoph R BeauloyeInstitut de Recherche Expérimentale et Clinique, Pole of Cardiovascular Research, Université catholique de Louvain, Brussels, Belgium.
Ioanna AndreadouLaboratory of Pharmacology, Faculty of Pharmacy, National and Kapodistrian University of Athens, Athens, Greece.
Marisol Ruiz-MeanaDepartment of Cardiology, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), CIBER-CV, Universitat Autonoma de Barcelona and Centro de Investigación Biomédica en Red-CV, Madrid, Spain.
Nichlas R JespersenDepartment of Cardiology, Aarhus University Hospital, Aarhus N, Denmark.
Duvaraka Kula-AlwarDepartment of Medicine, University of Cambridge, Cambridge, UK.
Hiran A PragDepartment of Medicine, University of Cambridge, Cambridge, UK.
Hans Eric BotkerDepartment of Cardiology, Aarhus University Hospital, Aarhus N, Denmark.
Maija DambrovaPharmaceutical Pharmacology, Latvian Institute of Organic Synthesis, Riga, Latvia.
Christophe MontessuitDepartment of Pathology and Immunology, University of Geneva School of Medicine, Geneva, Switzerland.
Tuuli KaambreLaboratory of Chemical Biology, National Institute of Chemical Physics and Biophysics, Tallinn, Estonia.
Edgars LiepinshPharmaceutical Pharmacology, Latvian Institute of Organic Synthesis, Riga, Latvia.
Paul S BrookesDepartment of Anesthesiology, University of Rochester Medical Center, Rochester, NY, USA.
Thomas KriegDepartment of Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0002-5192-580X
University of Cambridge · GBAarhus University Hospital · DKLatvijas Organiskās Sintēzes Institūts · LVAmsterdam Neuroscience · NLCliniques Universitaires Saint-Luc · BENational and Kapodistrian University of Athens · GRNational Institute of Chemical Physics and Biophysics · EEUCLouvain · BEUniversitat Autònoma de Barcelona · ESUniversity of Geneva · CHUniversity of Rochester Medical Center · US

Funding

NIH HHS R01-HL-071158
6 · The paper itself

Abstract

Reducing infarct size during a cardiac ischaemic-reperfusion episode is still of paramount importance, because the extension of myocardial necrosis is an important risk factor for developing heart failure. Cardiac ischaemia-reperfusion injury (IRI) is in principle a metabolic pathology as it is caused by abruptly halted metabolism during the ischaemic episode and exacerbated by sudden restart of specific metabolic pathways at reperfusion. It should therefore not come as a surprise that therapy directed at metabolic pathways can modulate IRI. Here, we summarize the current knowledge of important metabolic pathways as therapeutic targets to combat cardiac IRI. Activating metabolic pathways such as glycolysis (eg AMPK activators), glucose oxidation (activating pyruvate dehydrogenase complex), ketone oxidation (increasing ketone plasma levels), hexosamine biosynthesis pathway (O-GlcNAcylation; administration of glucosamine/glutamine) and deacetylation (activating sirtuins 1 or 3; administration of NAD

Indexed as

Molecular Targeted TherapyAnimalsEnergy MetabolismHumansMitochondria, HeartMyocardial InfarctionMyocardial Reperfusion InjuryMyocardiumischemiametabolismmitochondria

Identifiers

PMID32384583
PMCPMC7294140
OpenAlexW3022223885

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.