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Updated: May 11, 2025

Noninvasive Assessment of Cardiac Abnormalities in Experimental Autoimmune Myocarditis by Magnetic Resonance Microscopy Imaging in the Mouse
Published on: June 20, 2014
Immune Checkpoint Inhibitor Myocarditis and Left Ventricular Systolic Dysfunction
Yen-Chou Chen1, Charles Dolladille2, Anjali Rao3
1Division of Cardiology, University of California-San Francisco, San Francisco, California, USA; Division of Cardiology and Cardiovascular Research Center, Taipei Medical University Hospital, Taipei, Taiwan; Taipei Heart Institute, Taipei Medical University, Taipei, Taiwan.
Predictors of reduced left ventricular ejection fraction (LVEF <50%) in immune checkpoint inhibitor myocarditis (ICI-M) include dyspnea and prior heart failure. Reduced LVEF may be linked to increased 30-day mortality in ICI-M patients.
Area of Science:
- Cardiology
- Oncology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) have revolutionized cancer therapy.
- Immune checkpoint inhibitor myocarditis (ICI-M) is a serious, potentially fatal complication.
- Understanding predictors of reduced left ventricular ejection fraction (LVEF <50%) in ICI-M is crucial.
Purpose of the Study:
- Identify factors associated with LVEF <50% versus LVEF ≥50% at hospitalization for ICI-M.
- Evaluate the relationship between LVEF and 30-day all-cause mortality in ICI-M patients.
Main Methods:
- Retrospective analysis of the International ICI-Myocarditis Registry (n=757).
- Patients stratified by LVEF (<50% or ≥50%) on admission.
- Cox proportional hazards models and multivariable logistic regression used.
Main Results:
- 35% of patients had LVEF <50%.
- Predictors of LVEF <50% included younger age, lower BMI, chest radiation, BRAF/MEK inhibitors, pre-existing heart failure, dyspnea, and longer time from ICI initiation.
- Myositis symptoms were linked to LVEF ≥50%.
Conclusions:
- Dyspnea, time from ICI initiation, history of heart failure, and prior cardiotoxic therapy predict reduced LVEF in ICI-M.
- Reduced LVEF showed a marginal association with increased 30-day mortality.
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