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Updated: Jun 28, 2026

A Murine Closed-chest Model of Myocardial Ischemia and Reperfusion
Published on: July 17, 2012
Time-dependent effects of interleukin-1 blockade by anakinra in myocarditis and inflammatory cardiomyopathy
Giovanni Peretto1,2,3, Andrea Villatore1,2,3, Alessia Fausta Trezza3
1Multidisciplinary Disease Unit for Myocarditis and Arrhythmogenic Cardiomyopathies, IRCCS San Raffaele Scientific Institute, Via Olgettina 60, 20132, Milan, Italy.
Aims:
Interleukin-1 (IL-1) plays a central role in myocardial inflammation and adverse remodelling. However, the long-term clinical impact of IL-1 blockade in myocarditis and inflammatory cardiomyopathy (Infl-CMP), particularly according to treatment exposure and discontinuation, remains unclear. We evaluated time-dependent outcomes in patients treated with the IL-1 receptor antagonist anakinra.
Methods And Results:
We included 42 consecutive patients with definite myocarditis or Infl-CMP diagnosed by cardiac magnetic resonance either with or without endomyocardial biopsy. Mean age was 46 ± 17 years, 60% were male, and mean left ventricular ejection fraction (LVEF) at presentation was 43 ± 16%. Patients received anakinra (100 mg/day) for a median of 11 months and were followed for 51 ± 20 months. The primary endpoint was major adverse events (MAE), defined as cardiac death, heart transplantation, major ventricular arrhythmias, hospitalization for acute heart failure, or recurrent myocarditis. Time-updated Kaplan-Meier analysis showed a significant reduction in MAE during anakinra treatment compared with both pre-treatment and post-discontinuation phases (log-rank P < .001). Events were rare during active treatment, whereas most deaths (7/8) and all major ventricular arrhythmias occurred outside the treatment phase. Recurrent myocarditis was reduced during therapy (1/42 vs 9/32 pre-treatment; P = .002) and reappeared after discontinuation (3/37). Cardiac-related hospitalizations decreased during treatment and increased thereafter. These changes were paralleled by improvements in troponin, LVEF (≥5% in one-third), cardiac magnetic resonance inflammatory abnormalities, and arrhythmic burden. Outcomes differed according to aetiology.
Conclusion:
Anakinra was associated with a marked reduction in MAE during active treatment, with re-emergence after discontinuation, supporting a potential role for sustained IL-1 blockade in selected high-risk patients.
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