Related Experiment Video
Updated: Jul 17, 2025

Noninvasive Assessment of Cardiac Abnormalities in Experimental Autoimmune Myocarditis by Magnetic Resonance Microscopy Imaging in the Mouse
Published on: June 20, 2014
Similarities and differences between myocarditis following COVID-19 mRNA vaccine and multiple inflammatory syndrome
Donato Amodio1, Giuseppe Rubens Pascucci1, Nicola Cotugno1
1Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy; Department of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Insights
Cardiac adverse events following COVID-19 immunization (c-AEFI) and multisystem inflammatory syndrome in children (MIS-C) show distinct inflammatory profiles. c-AEFI patients exhibit higher myocardial injury markers and specific androgen levels, persisting over time.
Area of Science:
- Cardiology
- Immunology
- Pediatrics
Background:
- Cardiac adverse Events Following COVID-19 Immunization (c-AEFI) and Multisystem Inflammatory Syndrome in Children (MIS-C) with cardiac involvement are observed, particularly in young adult males.
- Understanding the distinct pathophysiological mechanisms of these post-immunization and post-infectious cardiac conditions is crucial.
Purpose of the Study:
- To compare the inflammatory profiles and specific biomarkers in patients with c-AEFI versus MIS-C with cardiac involvement.
- To investigate the presence of autoantibodies targeting cardiac and endothelial cells in these conditions.
Main Methods:
- Comparative analysis of inflammatory protein profiles between c-AEFI and MIS-C patient cohorts.
- Measurement of serum DHEAS, DHEA, and cortisone levels.
- Screening for anti-heart muscle and anti-endothelial cell antibodies.
Main Results:
- MIS-C patients showed higher levels of systemic inflammation proteins compared to c-AEFI patients.
- c-AEFI patients exhibited elevated levels of proteins associated with myocardial injury.
- Higher levels of DHEAS, DHEA, and cortisone were detected in c-AEFI patients, persisting at follow-up.
- No anti-heart muscle or anti-endothelial cell antibodies were found in either group.
Conclusions:
- c-AEFI and MIS-C with cardiac involvement present with distinct inflammatory and androgen profiles.
- c-AEFI appears to be a localized cardiac condition with a unique hormonal signature.
- These findings suggest different underlying mechanisms for cardiac complications following COVID-19 immunization versus MIS-C.
Abstract:
Despite the multiple benefits of vaccination, cardiac adverse Events Following COVID-19 Immunization (c-AEFI) have been reported. These events as well as the severe cardiac involvement reported in Multisystem inflammatory syndrome in children (MIS-C) appear more frequent in young adult males. Herein, we firstly report on the inflammatory profiles of patients experiencing c-AEFI in comparison with age, pubertal age and gender matched MIS-C with cardiac involvement. Proteins related to systemic inflammation were found higher in MIS-C compared to c-AEFI, whereas a higher level in proteins related to myocardial injury was found in c-AEFI. In addition, higher levels of DHEAS, DHEA, and cortisone were found in c-AEFI which persisted at follow-up. No anti-heart muscle and anti-endothelial cell antibodies have been detected. Overall current comparative data showed a distinct inflammatory and androgens profile in c-AEFI patients which results to be well restricted on heart and to persist months after the acute event.
Related Concept Videos
Myocarditis II: Clinical Features and Diagnostic Tests
Myocarditis I: Introduction
Myocarditis III: Medical Management
Myocarditis IV: Nursing Management
Pericarditis I: Introduction
Pericarditis II: Clinical Features and Diagnostic Tests

