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Early Gadolinium Enhancement for Determination of Area at Risk: A Preclinical Validation Study
Sophia Hammer-Hansen1, Steve W Leung2, Li-Yueh Hsu3
1Laboratory for Advanced Cardiovascular Imaging, National Heart, Lung, and Blood Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland; Department of Medicine B, The Heart Center, Rigshospitalet, Copenhagen, Denmark.
Early gadolinium enhancement (EGE) on cardiac magnetic resonance (CMR) accurately depicts the area at risk (AAR) in canine myocardial infarction models. EGE reflects both reversible and irreversible myocardial injury, correlating well with microsphere blood flow analysis.
Area of Science:
- Cardiovascular imaging
- Myocardial infarction research
- Diagnostic techniques in cardiology
Background:
- Controversy exists regarding whether cardiac magnetic resonance (CMR) enhancement in acute myocardial infarction solely represents irreversibly injured myocardium.
- Early gadolinium enhancement (EGE) is proposed to measure the area at risk (AAR) in acute myocardial infarction, correlating with T2-weighted imaging, but requires pathological validation.
Purpose of the Study:
- To determine if early gadolinium enhancement (EGE) via cardiac magnetic resonance (CMR) accurately depicts the area at risk (AAR) in a canine model of reperfused myocardial infarction.
- To validate EGE as a measure of AAR using microsphere blood flow analysis.
Main Methods:
- Eleven dogs underwent 2 hours of coronary artery occlusion followed by 48 hours of reperfusion.
- EGE imaging was performed 3 minutes post-contrast, with late gadolinium enhancement imaging between 10-15 minutes.
- Area at risk (AAR) was defined by microsphere blood flow analysis (<2 SD from remote myocardium); infarct size was determined by triphenyltetrazolium chloride.
Main Results:
- EGE size showed no significant difference compared to AAR by microspheres (44.1 ± 15.8% vs. 42.7 ± 9.2%, p=0.61) with strong correlation (r=0.88, p<0.001).
- EGE size was significantly larger than infarct size determined by triphenyltetrazolium chloride and late gadolinium enhancement (p<0.001 for both).
- No difference was observed between EGE size and enhancement on native T1 and T2 maps.
Conclusions:
- Early gadolinium enhancement (EGE) at 3 minutes post-contrast correlates well with the area at risk (AAR) determined by microsphere analysis in reperfused myocardial infarction.
- EGE reflects both reversibly and irreversibly injured myocardium, indicating it represents the AAR rather than solely infarct size.
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