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Published on: April 17, 2021
Iron Status and Short-Term Recovery after Non-Severe Acute Myocarditis: A Prospective Observational Study
Paweł Franczuk1,2, Michał Tkaczyszyn1,2, Aneta Kosiorek1
1Institute of Heart Diseases, Wroclaw Medical University, 50-556 Wroclaw, Poland.
Altered iron status in acute myocarditis (MCD) patients normalizes within six weeks. Low iron and transferrin saturation (TSAT) during hospitalization correlate with neurohormonal activation and persistent left ventricular dysfunction.
Area of Science:
- Cardiology
- Hematology
- Pathophysiology
Background:
- Myocarditis (MCD) recovery and progression to cardiomyopathy mechanisms are unclear.
- Iron impacts inflammation and cardiomyocyte energy metabolism, potentially influencing inflammatory myocardial disease.
- Systemic iron parameters' role in MCD pathophysiology requires investigation.
Purpose of the Study:
- To assess the relationship between systemic iron parameters and myocardial dysfunction in acute myocarditis patients.
- To evaluate iron status changes during hospitalization and post-discharge follow-up.
- To correlate iron status with clinical, laboratory, and echocardiographic indices.
Main Methods:
- Prospective enrollment of 42 hospitalized MCD patients and healthy controls.
- Assessment of iron status (serum ferritin, hepcidin, iron, TSAT) during hospitalization and 6 weeks post-discharge.
- Evaluation of clinical, laboratory (NT-proBNP), and echocardiographic (LVEF, GLS) indices.
Main Results:
- MCD patients exhibited higher serum ferritin/hepcidin and lower serum iron/TSAT than controls (p < 0.01).
- Iron status normalized by 6 weeks post-discharge.
- Lower in-hospital serum iron and TSAT correlated with higher NT-proBNP (p < 0.05) and persistent lower LVEF and worse GLS (p < 0.05).
Conclusions:
- Acute MCD alters iron status, which recovers within six weeks.
- Low serum iron and TSAT in acute MCD are linked to increased in-hospital neurohormonal activation.
- These iron derangements correlate with subtle, persistent left ventricular dysfunction post-myocarditis.
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