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Vitamin C may reduce troponin and CKMB levels after PCI and CABG: a meta-analysis
Sander Rozemeijer1,2, Harri Hemilä3, Marlinde van Baaren4
1Department of Intensive Care Medicine, Research VUmc Intensive Care (REVIVE), Amsterdam Cardiovascular Science (ACS), Amsterdam Infection and Immunity Institute (AI&II), Amsterdam Medical Data Science (AMDS), Amsterdam UMC, Location VUmc, Vrije Universiteit Amsterdam, De Boelelaan 1117, Amsterdam, 1081 HV, The Netherlands. s.rozemeijer@amsterdamumc.nl.
Insights
Vitamin C may reduce cardiac enzyme levels following heart procedures like PCI and CABG. This antioxidant effect helps protect against periprocedural myocardial injury, suggesting potential benefits for patients.
Area of Science:
- Cardiology
- Biochemistry
- Nutritional Science
Background:
- Periprocedural myocardial injury (PMI) after PCI or CABG increases cardiovascular risk.
- Biomarkers like troponin (Tn) and creatine kinase-MB (CKMB) indicate PMI.
- Vitamin C's antioxidant properties may mitigate ischemia/reperfusion injury.
Approach:
- Systematic meta-analysis of seven controlled clinical trials.
- Included 872 adult patients undergoing PCI or CABG.
- Analyzed effects of intravenous vitamin C on Tn, CKMB, and oxidative stress biomarkers.
Key Points:
- Vitamin C administration prior to PCI/CABG significantly reduced peak Tn levels by 43% and peak CKMB levels by 14%.
- Intravenous vitamin C, ranging from 1 to 16 g/day, demonstrated efficacy.
- Reduced biomarkers of oxidative stress were also observed.
Conclusions:
- Vitamin C shows potential in decreasing cardiac enzyme levels post-PCI/CABG.
- Antioxidant mechanisms likely contribute to the observed cardioprotective effects.
- Further research is warranted to determine optimal dosing and clinical applications.
Background:
Ischemia/reperfusion injury contributes to periprocedural myocardial injury (PMI) in patients undergoing percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG). PMI can be estimated by the elevation of troponin (Tn) and creatine kinase-MB (CKMB) plasma levels, and it is associated with increased risk of cardiovascular events and mortality. Vitamin C might have a beneficial effect on PMI by improving endothelial function, improving myocardial perfusion, and by reducing oxidative stress generated during/after reperfusion. In several small animal models of cardiac stress, vitamin C reduced the increase in Tn and CKMB levels. The aim of this meta-analysis was to investigate whether vitamin C administration may have an effect on Tn and CKMB levels in patients undergoing PCI or CABG.
Methods:
We searched PubMed, Cochrane, Embase and Scopus databases for controlled clinical trials reporting on Tn and CKMB levels in adult patients who underwent PCI or CABG and received vitamin C. As secondary outcomes we collected data on biomarkers of oxidative stress in the included trials. In our meta-analysis, we used the relative scale and estimated the effect as the ratio of means.
Results:
We found seven controlled trials which included 872 patients. All included trials administered vitamin C intravenously, with a range from 1 to 16 g/day, and all initiated vitamin administration prior to the procedure. Vitamin C decreased peak Tn plasma levels in four trials on average by 43% (95% CI: 13 to 63%, p = 0.01) and peak CKMB plasma levels in five trials by 14% (95% CI: 8 to 21%, p < 0.001). Vitamin C also significantly decreased the biomarkers of oxidative stress.
Conclusions:
Vitamin C may decrease cardiac enzyme levels in patients undergoing elective PCI or CABG. This may be explained partially by its antioxidant effects. Our findings encourage further research on vitamin C administration during cardiac procedures and in other clinical contexts that increase the level of cardiac enzymes. Future studies should search for an optimal dosing regimen, taking baseline and follow-up plasma vitamin C levels into account.
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