Key result
Unrecognized non-infarct-related myocardial scar linked to ~245% higher MACE risk in AMI patients.
Why the study?
The prognostic impact of unrecognized non-infarct-related myocardial scar detected by cardiac MRI in patients with acute myocardial infarction was unclear.
Does the presence of unrecognized non-infarct-related myocardial scar on cardiac MRI predict MACE in patients with a first clinical episode of acute myocardial infarction?
Cohort (n=269)
Does the presence of unrecognized non-infarct-related myocardial scar on cardiac MRI predict MACE in patients with a first clinical episode of acute myocardial infarction?
Hazard Ratio: 3.45 (95% CI 1.03–11.47)
Absolute Event Rate: 22.9% vs 6.8%
p-value: p=< 0.01
In patients with a first AMI, unrecognized non-infarct-related myocardial scar on cardiac MRI is a strong independent predictor of future major adverse cardiac events.
Aims: Unrecognized myocardial scar by late gadolinium enhancement (LGE) magnetic resonance imaging (MRI) is strongly associated with cardiac event in patients with stable coronary artery disease. The purpose of this study was to evaluate the prognostic impact of unrecognized non-infarct-related LGE (non-IR-LGE) in patients with acute myocardial infarction (AMI). Methods and results: We studied 269 patients with a first clinical episode of AMI underwent cardiac MRI within 6 weeks after onset (209 men; age, 66 ± 12 years). LGE, cine MRI and T2-weighted imaging were obtained to evaluate the presence and extent of LGE and to evaluate cardiac function. Major adverse cardiac events (MACE) were defined as cardiovascular death, non-fatal AMI, unstable angina requiring revascularization, fatal arrhythmia, and heart failure. Unrecognized non-IR LGE was observed in 13.0% of patients. During follow-up periods (median, 22 months; range, 3-95 months), 8.9% of patients experienced MACE in this study. In addition, 22.9% of patients with unrecognized non-IR LGE and 6.8% of patients without unrecognized non-IR-LGE experienced MACE (P < 0.01). The presence of unrecognized non-IR LGE predicted MACE with a hazard ratio of 3.45 (95% confidential interval, 1.03-11.47; P < 0.01). In addition, unrecognized non-IR LGE was the strongest independent predictors of MACE with a hazard ratio of 3.30 by the Cox proportional hazards model (P < 0.01). In contrast, angiography-proven multi-vessel disease and transmural extent of infarct-related LGE were not independently associated with MACE. Conclusion: Among patients with a first clinical episode of AMI, unrecognized non-IR myocardial scar provides incremental prognostic value for predicting MACE beyond that of common clinical, angiographic and functional variables.
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Omori et al. (2017) conducted a cohort in Acute myocardial infarction (n=269). Unrecognized non-infarct-related myocardial scar (non-IR-LGE) vs. Absence of unrecognized non-IR-LGE was evaluated on Major adverse cardiac events (MACE) including cardiovascular death, non-fatal AMI, unstable angina requiring revascularization, fatal arrhythmia, and heart failure (HR 3.45, 95% CI 1.03-11.47, p=< 0.01). Unrecognized non-infarct-related myocardial scar predicted major adverse cardiac events in patients with acute myocardial infarction (22.9% vs 6.8%; HR 3.45; 95% CI 1.03-11.47; P<0.01).
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