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Colchicine effect on biomarkers of cardiac remodelling and atherosclerosis in ST-elevation myocardial infarction: A
Hanan Ahmed Hassanain1, Lamia Mohamed El Wakeel2, Hazem Khorshid3
1Ain Shams University Specialized Hospital, Cairo, Egypt.
Insights
Colchicine shows promise in reducing triglyceride levels and the triglyceride/HDL-C ratio in ST-elevation myocardial infarction (STEMI) patients. This anti-inflammatory drug was well-tolerated and may impact atherosclerosis and cardiac remodelling post-STEMI.
Area of Science:
- Cardiology
- Inflammation Research
- Atherosclerosis Studies
Background:
- Atherosclerotic cardiovascular disease, driven by inflammation, is a leading cause of mortality.
- ST-elevation myocardial infarction (STEMI) carries a high risk of subsequent cardiovascular events and mortality.
- Investigating novel therapeutic targets for post-STEMI management is crucial.
Purpose of the Study:
- To evaluate the efficacy of colchicine in mitigating inflammation, cardiac remodelling, and atherosclerotic risk factors in STEMI patients.
- To assess colchicine's impact on specific biomarkers including sST2, interleukin-1β, lipid profiles, and left ventricular ejection fraction.
Main Methods:
- A randomized controlled trial involving 88 STEMI patients post-percutaneous coronary intervention.
- Patients received either standard care or standard care plus 0.5 mg colchicine twice daily for 3 months.
- Key parameters were measured at baseline and after 3 months of treatment.
Main Results:
- Colchicine significantly reduced triglyceride (TG) levels and the TG/high-density lipoprotein cholesterol (HDL-C) ratio.
- No significant changes were observed in sST2, interleukin-1β levels, or left ventricular ejection fraction.
- sST2 levels positively correlated with TG/HDL-C ratio at follow-up.
Conclusions:
- Colchicine demonstrates a beneficial effect on lipid metabolism, specifically reducing TG and TG/HDL-C ratio in STEMI patients.
- The drug was found to be safe and well-tolerated in this patient cohort.
- Larger, long-term studies are warranted to confirm colchicine's clinical impact on cardiac remodelling outcomes post-STEMI.
Aims:
Owing to its underlying inflammatory nature, atherosclerotic cardiovascular disease remains the leading global cause of mortality, particularly post-ST-elevation myocardial infarction (STEMI), a condition with significant risk for further cardiovascular events and mortality. This study aimed to investigate colchicine's effect on inflammation, cardiac remodelling and atherosclerotic risk in STEMI patients.
Methods:
We conducted a randomized controlled study on 88 STEMI patients undergoing percutaneous coronary intervention. Eligible patients were randomly assigned to 1 of 2 groups. The control group received the guideline-directed medical therapy for STEMI, and the test group received guideline-directed medical therapy and 0.5 mg colchicine twice daily for 3 months. The soluble suppressor of tumorigenicity (sST2), interleukin-1β, lipid profile parameters, triglyceride (TG)/high-density lipoprotein (HDL-C) ratio levels and left ventricular ejection fraction were evaluated for patients at baseline and the end of the 3 months.
Results:
No significant effects were reported for colchicine on sST2, interleukin-1β levels or left ventricular ejection fraction. Colchicine significantly lowered TG levels vs. controls, 134 (46-353) vs. 176 (72-825) respectively, P = .02, as well as TG/HDL-C ratio levels, 4.16 (2.75-5.24) vs. 5.11 (3.51-8.33),` respectively, P = .024. sST2 levels of the studied cohort were positively correlated with their TG/HDL-C ratio levels (R = .459, P < .001) at the end of follow-up.
Conclusion:
Our study highlights a promising impact of colchicine on atherosclerosis and cardiac remodelling factors in STEMI patients. Colchicine significantly reduced TG levels and TG/HDL-C ratio and was safe and well tolerated. Larger long-term studies powered to assess clinical outcomes of remodelling are necessary to confirm its beneficial effects in STEMI.
Gov Registration Id:
NCT06054100.
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