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Published on: January 21, 2018
Myocardial inflammation after elective percutaneous coronary intervention
Ioannis Merinopoulos1, U Bhalraam1, Bahman Kasmai2
1Norwich Medical School, University of East Anglia, UK; Department of Cardiology, Norfolk and Norwich University Hospital, UK.
Insights
This study investigated myocardial inflammation after percutaneous coronary intervention (PCI) using ultrasmall superparamagnetic particles of iron oxide (USPIO)-enhanced cardiovascular magnetic resonance (CMR). While a small increase in inflammation was observed, it was not statistically significant, suggesting potential for future research.
Area of Science:
- Cardiology
- Medical Imaging
- Inflammation Research
Background:
- Inflammation is central to percutaneous coronary intervention (PCI) sequelae.
- Myocardial inflammation, beyond the vessel wall, is increasingly recognized.
- Previous studies primarily focused on vascular inflammation post-angioplasty.
Purpose of the Study:
- To investigate myocardial inflammation following elective, uncomplicated PCI.
- To utilize ultrasmall superparamagnetic particles of iron oxide (USPIO)-enhanced cardiovascular magnetic resonance (CMR).
- To assess changes in blood biomarkers alongside CMR findings.
Main Methods:
- USPIO-enhanced CMR was performed on stable angina patients two weeks post-PCI.
- A control group of healthy volunteers was included for comparison.
- Blood biomarkers were measured at baseline, 4 hours, and two weeks post-PCI.
Main Results:
- A small, non-statistically significant increase in R2∗ values was observed in the PCI-affected myocardium.
- No significant difference in R2∗ values was found compared to remote or healthy myocardium.
- PTX3 and IL-6 levels increased significantly, peaking at 4 hours post-PCI.
Conclusions:
- USPIO-enhanced CMR was employed for the first time to assess myocardial inflammation post-elective PCI.
- A minor, non-significant increase in myocardial inflammation was detected.
- This methodology shows promise for future studies targeting post-PCI inflammation.
Objective:
It is well established that inflammation plays a central role in the sequelae of percutaneous coronary intervention (PCI). Most of the studies to date have focused on the inflammatory reaction affecting the vessel wall after angioplasty. However, there are data to suggest that the main foci of inflammation are in fact in the myocardium beyond the vessel wall. The main aim of our study was to investigate the myocardial inflammation after elective, uncomplicated angioplasty with cardiovascular magnetic resonance (CMR) enhanced by ultrasmall superparamagnetic particles of iron oxide (USPIO) and also blood biomarkers. This is the first study to report such findings after elective angioplasty.
Methods:
We assessed patients undergoing elective angioplasty for stable angina with USPIO-enhanced CMR two weeks after the procedure and compared the results with those of healthy volunteers who constituted the control group. We excluded patients with previous myocardial infarction, previous PCI, or any significant inflammatory condition. All patients also underwent blood biomarker testing at baseline (pre-PCI), 4 h, and two weeks later.
Results:
A total of five patients and three controls were scanned. There was a small absolute increase, although statistically insignificant, in R2∗ values in the PCI area compared with either remote myocardium from the same patient (PCI area [left anterior descending artery (LAD)] vs remote myocardium [circumflex area]: 19.3 ± 10.8 vs 9.2 ± 7.9, p = 0.1) or healthy myocardium from healthy volunteers (PCI area [LAD] vs healthy myocardium [LAD]: 19.3 ± 10.8 vs 12.2 ± 4.0, p = 0.2). PTX3 and IL-6 were the only biomarkers that changed significantly from baseline to 4 h and 2 weeks. Both biomarkers peaked at 4 h.
Conclusion:
We used USPIO-enhanced CMR for the first time to assess myocardial inflammation after elective, uncomplicated PCI. We have demonstrated a small numerical increase in inflammation, which was not statistically significant. This study opens the way for future studies to use this method as a means to target inflammation.
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