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Impact of quercetin in patients with myocardial infarction. A multicenter, randomized, and open-label pilot study

Sergey Kozhukhov, Alexander Parkhomenko, Yaroslav Lutay, Nataliia Dovganych, Study Investigators
Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese 2024 76:68-74

Bibliography

PubMed
PMID 37567562
Funding
Funding was not specified in the indexed record or the disclosure metadata available for this entry.
Competing interests
A competing-interest declaration was not available in the indexed record or the disclosure metadata used for this entry.

Study snapshot

DesignRandomized open-label multicenter pilot trial
ModelHuman intervention research
Sample143 adults with acute anterior STEMI; 70 intervention and 73 control
InterventionIntravenous quercetin plus standard reperfusion care versus standard care
DurationInfusions before reperfusion and over the following 5 days
EndpointsProtein activity, binding or signaling

What the study showed, in plain terms

Published in 2024, this source examined cardiovascular and metabolic health. Design: Randomized open-label multicenter pilot trial. Sample/model: 143 adults with acute anterior STEMI; 70 intervention and 73 control. The exposure or intervention was Intravenous quercetin plus standard reperfusion care versus standard care. Follow-up or treatment period: Infusions before reperfusion and over the following 5 days.

The intervention reduced enzyme-based infarct-size measures and intramyocardial hemorrhage. Ejection fraction and remodeling measures did not differ.

Hospital-based intravenous formulation and open-label pilot design. Findings cannot be transferred to oral supplement capsules.

Continue with Quercetin Data Center

For topic-level interpretation, read Quercetin for Weight Loss, Blood Sugar and Fatty Liver: Human Evidence. This is a related guide; the citation panel separately identifies articles that directly cite this paper.

Key findings

  • The intervention reduced enzyme-based infarct-size measures and intramyocardial hemorrhage.
  • Ejection fraction and remodeling measures did not differ.
  • The recorded outcome domains were Protein activity, binding or signaling.
  • The result applies to the tested exposure: Intravenous quercetin plus standard reperfusion care versus standard care; Infusions before reperfusion and over the following 5 days.

What this study can and cannot tell us

  • Hospital-based intravenous formulation and open-label pilot design. Findings cannot be transferred to oral supplement capsules.
  • Without a sufficiently blinded concurrent control, time effects, expectations, co-interventions and regression toward the mean can explain part of an apparent improvement.
  • Source basis: Source check: PubMed abstract and indexed metadata; full methods were not independently confirmed for this entry. Missing method details, funding information or participant denominators are not inferred.

Editorial review

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