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Interleukin-1 blockade treatment decreasing cardiovascular risk
Zi-Heng Zheng1, Xun Zeng1,2, Xiao-Ying Nie1,2
1Department of Cardiology, The First Affiliated Hospital, Sun Yat-Sen University and Key Laboratory on Assisted Circulation, NHC, Guangzhou, China.
Interleukin-1 (IL-1) blockage therapy reduces the risk of major adverse cardiovascular events (MACE), unstable angina, and heart failure. However, it did not significantly impact all-cause death or acute myocardial infarction (MI).
Area of Science:
- Cardiovascular Medicine
- Immunology
- Pharmacology
Background:
- Interleukin-1 (IL-1) is implicated in the pathogenesis of atherosclerosis and cardiovascular events.
- The precise impact of IL-1 blockage on cardiovascular risk reduction requires further clarification.
Purpose of the Study:
- To evaluate the efficacy of Interleukin-1 (IL-1) blockage in reducing the risk of major adverse cardiovascular events (MACE).
- To assess the effect of IL-1 blockage on all-cause death, acute myocardial infarction (MI), unstable angina, and heart failure incidence.
Main Methods:
- A systematic literature search was conducted using MEDLINE from January 1, 2005, to April 1, 2018.
- Included randomized controlled trials (RCTs) provided data on sample size and event occurrences in both treatment and placebo groups.
Main Results:
- Eight RCTs with 15,647 participants were analyzed.
- IL-1 blockage significantly decreased the risk of overall MACE (RR 0.88), unstable angina (RR 0.80), and heart failure recurrence (RR 0.44).
- No significant association was observed for IL-1 blockage with all-cause death (RR 0.91) or acute MI (RR 0.85).
Conclusions:
- IL-1 blockage demonstrates a significant reduction in risks for overall MACE, unstable angina, and heart failure.
- IL-1 blockage therapy did not show a significant effect on reducing all-cause mortality or acute myocardial infarction.
- Specific IL-1 inhibitors like anakinra and canakinumab showed varied effects on different cardiovascular outcomes.
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