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Losartan and prednisolone for post-COVID syndrome and cardiac inflammation: a randomized, double-blind,
Valentina O Puntmann1,2, Eike Nagel3,4,5, Dietrich Beitzke6
1DZHK Centre for Cardiovascular Imaging, Institute for Experimental and Translational Cardiovascular Imaging, German Centre for Cardiovascular Research - Partner Site Rhein-Main, Goethe University Frankfurt, Frankfurt am Main, Germany. puntmann@med.uni-frankfurt.de.
Insights
This clinical trial found no significant improvement in left ventricular ejection fraction for post-COVID inflammatory cardiac syndrome treated with losartan and prednisolone. The treatment was safe but did not meet the primary endpoint for cardiac function.
Area of Science:
- Cardiology
- Infectious Diseases
- Immunology
Background:
- Persistent cardiac symptoms are frequent in post-COVID syndrome, linked to immune dysregulation and inflammation.
- Existing treatments for inflammatory cardiac involvement in post-COVID syndrome are lacking.
- Cardiovascular magnetic resonance identifies inflammatory cardiac involvement.
Purpose of the Study:
- To evaluate the efficacy of losartan plus prednisolone versus placebo in treating inflammatory cardiac involvement in post-COVID syndrome.
- To assess the impact of the intervention on left ventricular ejection fraction and other cardiac parameters.
Main Methods:
- A multicenter, double-blind, randomized clinical trial (Myoflame-19) involving 279 participants.
- Participants received either losartan plus prednisolone or matching placebos for 16 weeks.
- The primary endpoint was the change in left ventricular ejection fraction, assessed via cardiovascular magnetic resonance.
Main Results:
- The treatment demonstrated a neutral effect on the primary endpoint (change in left ventricular ejection fraction).
- Secondary endpoints showed numerical improvements in symptoms and imaging, but confidence intervals included the null value.
- The intervention was safe and well-tolerated by participants.
Conclusions:
- Losartan plus prednisolone did not significantly improve left ventricular ejection fraction in patients with inflammatory cardiac involvement post-COVID-19.
- Findings suggest the need for further research into targeted immunomodulation for post-COVID cardiac complications.
- The study provides valuable data for designing future clinical trials in this patient population.
Abstract:
Persistent cardiac symptoms are common in post-COVID syndrome, even without structural heart disease. Evidence implicates immune dysregulation, endothelial dysfunction and low-grade cardiovascular inflammation. Yet no targeted treatment exists. Myoflame-19 is a multicenter, double-blind clinical trial of 279 participants with inflammatory cardiac involvement defined by cardiovascular magnetic resonance, randomized 1:1 to losartan plus prednisolone (n = 139) or matching placebos (n = 140) for 16 weeks. The modified intention-to-treat population comprised 124 and 122 participants. The primary endpoint, change in left ventricular (LV) ejection fraction, was neutral: between-group difference 0.74 percentage points (pp), 95%CI -0.14 to 1.62, p = 0.10, unpaired t-test; supportive baseline-adjusted ANCOVA 0.99, 95%CI 0.15-1.83, p = 0.021. Among prespecified secondary endpoints, several symptom and imaging measures showed numerical differences favoring intervention, including Average Symptom Score components (modified Canadian Chest Pain Scale -4.8 pp, 95%CI -17.3 to 7.6; NYHA class -8.1 pp, -20.6 to 4.3; Long COVID symptom burden -7.7 pp, -18.9 to 3.6), native T1 and T2 values (native T1 -2.46 ms, -8.35 to 3.42; native T2 -0.31 ms, -1.16 to 0.53), and LV end-diastolic volume ( + 1.45 ml/m², -0.09 to 3.00); however, confidence intervals included the null value and these findings should be regarded as hypothesis-generating.Treatment was safe and well-tolerated. These findings indicate a neutral treatment effect on the primary endpoint. They inform targeted immunomodulation and design of future trials in post-COVID syndrome and inflammatory cardiac involvement. Trial registration: EudraCT 2022-001682-12; NCT05619653.
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