Anakinra to Prevent Adverse Post-infarction Remodeling (2)
Overview
- Phase
- Phase 2
- Intervention
- Anakinra
- Conditions
- Acute Myocardial Infarction
- Sponsor
- Virginia Commonwealth University
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Difference Between the Anakinra Arm and the Placebo Arm in Change in Left Ventricular End-systolic Volume Indices
- Status
- Completed
- Last Updated
- 9 years ago
Overview
Brief Summary
Acute myocardial infarction (AMI) remains a major cause of morbidity and mortality. Many patients die early during the course, and those who survive are at risk for dying late from adverse cardiac remodeling and heart failure.
The initial ischemic damage to the myocardium initiates an intense inflammatory response in promoting further cardiac dysfunction and heart failure. The investigators propose that an antiinflammatory strategy based on blockade of Interleukin-1 will quench the inflammatory response and lead to a more favorable cardiac remodeling process.
Detailed Description
Acute myocardial infarction (AMI) remains a major cause of morbidity and mortality. Many patients die early during the course, and those who survive are at risk for dying late from adverse cardiac remodeling and heart failure. The initial ischemic damage to the myocardium initiates an intense inflammatory response in promoting further cardiac dysfunction and heart failure. Interleukin-1 (IL-1) is the prototypical inflammatory cytokine involved in the tissue response to injury. In the experimental model of large anterior wall AMI in the mouse, IL-1 blockade using anakinra, a recombinant human IL-1 receptor antagonist ameliorates cardiac remodeling and improves survival following AMI. Although the mouse AMI model is helpful in understanding the events leading to adverse post-infarction cardiac remodeling and heart failure, the exact role of IL-1 in patients with AMI has not been completely characterized. The investigators propose to address this question by studying patients presenting with ST-segment elevation AMI (STEMI). Such patients are at high risk for in-hospital and long-term mortality and display several markers of inflammation. The investigators hypothesize that IL-1 blockade in patients STEMI with will limit the acute inflammatory response and prevent adverse cardiac remodeling, heart failure, and related morbidity. The investigators hypothesize that treatment with anakinra will lead to more favorable cardiac remodeling. Left ventricular end-systolic volume index (LVESVi) is the preferred clinical marker of adverse cardiac remodeling and a strong predictor of heart failure-related mortality in patients with STEMI, and will be used as primary endpoint of the study. The investigators propose that anakinra will reduce the change in LVESVi from baseline to 10-14 weeks after STEMI, and will prevent, at least in part, other changes in cardiac function and exercise tolerance associated with adverse cardiac remodeling and heart failure.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients with STEMI will be asked to enroll according to the following inclusion criteria:
- •age \> 18 years,
- •acute (\<12 h) onset of chest pain associated with ST segment elevation (\>2 mm) in 2 or more anatomically contiguous leads at ECG,
- •and successful primary percutaneous coronary intervention.
- •Exclusion criteria:
- •inability to give informed consent,
- •late presentation (\>12 h),
- •unsuccessful revascularization procedure,
- •hemodynamic instability including hypotension,
- •prior Q-wave AMI,
Exclusion Criteria
- Not provided
Arms & Interventions
Anakinra
Anakinra 100 mg injectable subcutaneously daily
Intervention: Anakinra
Placebo
0.67 ml of sodium chloride (NaCl) 0.9% solution
Intervention: Placebo
Outcomes
Primary Outcomes
Difference Between the Anakinra Arm and the Placebo Arm in Change in Left Ventricular End-systolic Volume Indices
Time Frame: 10-14 weeks minus baseline
Change in n left ventricular end-systolic volume indices from baseline to follow up exam at cardiac magnetic resonance imaging comparing anakinra- and placebo-treated patients.
Secondary Outcomes
- Difference Between the Anakinra Arm and the Placebo Arm in Change in Left Ventricular End-diastolic Volume Indices From Baseline to Follow up Exam at Cardiac Magnetic Resonance Imaging(10-14 weeks)
- Percentage of Patients in Each Group With Reverse Remodeling (Reduction in LVESVi >5%)(10-14 weeks)
- Median Difference Between the 2 Arms in the Peak Oxygen Consumption (VO2) at 10-14 Weeks(10-14 weeks)
- Incidence of Heart Failure(10-14 weeks)
- Number of Adverse Events in Each Group(10-14 weeks)
- Difference Between the 2 Arm in the Interval Change in Right Ventricular Ejection Fraction (RVEF)(10-14 weeks)
- Difference Between the Anakinra Arm and the Placebo Arm in Change in Left Ventricular Ejection Fraction Values From Baseline to Follow up Exam at Cardiac Magnetic Resonance Imaging(10-14 weeks)
- Median Difference Between the 2 Arms in the Ratio of Minute Ventilation and Carbon Dioxide Production (VE/VCO2 Slope) at 10-14 Weeks(10-14 weeks)
- Percentage of Patients in Each Group With Reverse Remodeling (Reduction in LVESVi >10%)(10-14 weeks)
- Percentage of Patients in Each Group With Adverse Remodeling (LVESVi Increase >5%) Based Upon Cardiac Magnetic Resonance Imaging(10-14 weeks)
- Percentage of Patients in Each Group With Adverse Remodeling (LVESVi Increase >10%)(10-14 weeks)
- Percentage of Patients in Each Group With Left Ventricular Ejection Fraction Change >5%(10-14 weeks)
- Percentage of Patients in Each Group With Left Ventricular Ejection Fraction Change >10%(10-14 weeks)
- Number of Deaths in Each Group(10-14 weeks)
- Number of Adverse Events Requiring Withdrawal in Each Group(10-14 weeks)