Key result
Signal intensity percent infarct mapping (SI-PIM) accurately determined myocardial infarct volume compared to TTC reference regardless of the pathological stage of MI.
Why the study?
Does signal intensity percent infarct mapping (SI-PIM) accurately determine myocardial infarct size compared to TTC staining in a swine model of reperfused MI?
Does signal intensity percent infarct mapping (SI-PIM) accurately determine myocardial infarct size compared to TTC staining in a swine model of reperfused MI?
p-value: p=0.073, 0.091, 0.73
The SI-PIM method using LGE MRI accurately determines myocardial infarct volume regardless of the pathological stage of MI in a swine model.
SI-PIM accurately sizes MI independent of infarct stage in swine; extends validation of partial-volume mapping beyond acute phase for translational research.
PURPOSE: To test whether signal intensity percent infarct mapping (SI-PIM) accurately determines the size of myocardial infarct (MI) regardless of infarct age. MATERIALS AND METHODS: Forty-five swine with reperfused MI underwent 1.5T late gadolinium enhancement (LGE) magnetic resonance imaging (MRI) after bolus injection of 0.2 mmol/kg Gd(DTPA) on days 2-62 following MI. Animals were classified into acute, healing, and healed groups by pathology. Infarct volume (IV) and infarct fraction (IF) were determined by two readers, using binary techniques (including 2-5 standard deviations [SD] above the remote, and full-width at half-maximum) and the SI-PIM method. Triphenyl-tetrazolium-chloride staining (TTC) was performed as reference. Bias (percent under/overestimation of IV relative to TTC) of each quantification method was calculated. Bland-Altman analysis was done to test the accuracy of the quantification methods, while intraclass correlation coefficient (ICC) analysis was done to assess intra- and interobserver agreement. RESULTS: Bias of the MRI quantification methods do not depend on the age of the MI. Full-width at half-maximum (FWHM) and SI-PIM gave the best estimate of MI volume determined by the reference TTC (P-values for the FWHM and SI-PIM methods were 0.183, 0.26, 0.95, and 0.073, 0.091, 0.73 in Group 1, Group 2, and Group 3, respectively), while using any of the binary thresholds of 2-4 SDs above the remote myocardium showed significant overestimation. The 5 SD method, however, provided similar IV compared to TTC and was shown to be independent of the size and age of MI. ICC analysis showed excellent inter- and intraobserver agreement between the readers. CONCLUSION: Our results indicate that the SI-PIM method can accurately determine MI volume regardless of the pathological stage of MI. Once tested, it may prove to be useful for the clinic.
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Lenkey et al. (2015) studied reperfused myocardial infarction (n=45). Signal intensity percent infarct mapping (SI-PIM) vs. Triphenyl-tetrazolium-chloride staining (TTC) was evaluated on Bias (percent under/overestimation of infarct volume relative to TTC) (p=0.073, 0.091, 0.73). Signal intensity percent infarct mapping (SI-PIM) accurately determined myocardial infarct volume compared to TTC reference regardless of the pathological stage of MI.
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