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Updated: Aug 6, 2026

MRI and PET in Mouse Models of Myocardial Infarction
Published on: December 19, 2013
Percent infarct mapping: an R1-map-based CE-MRI method for determining myocardial viability distribution
Pál Surányi1, Pál Kiss, Brigitta C Brott
1Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, Alabama 35294-0005, USA.
Abstract:
Viability detection is crucial for the management of myocardial infarction (MI). Signal intensity (SI)-based MRI methods may overestimate infarct size in vivo. In contrast to SI, the longitudinal relaxation-rate enhancement (DeltaR1) is an intrinsic parameter that is linearly proportional to the concentration of contrast agent (CA). Determining DeltaR1 in the presence of an infarct-avid persistent CA (PCA) allows determination of the per-voxel percentage of infarcted tissue. Introduced here is a DeltaR1-based CE-MRI method, termed percent infarct mapping (PIM), for quantifying myocardial viability following delayed PCA accumulation. In a canine MI model (N=6), PIMs were generated using a persistent CA (PCA) and validated using triphenyltetrazolium-chloride (TTC) histochemistry. Voxel-by-voxel R1 maps of the entire left ventricle (LV) were generated 24 and 48 hr after PCA administration using inversion recovery (IR) with multiple inversion times (TIs). PI values were calculated voxel by voxel. Significant correlations (P<0.01, R=0.97) were obtained for PI per slice (PIS) determined using PIM vs. corresponding TTC-based values. Median deviations of PIS with PIM from that with TTC were only 1.01% and -0.53%, at 24 hr and 48 hr. Median deviations from the true infarction fraction (IF) were 1.23% and 0.49% of LV at 24 hr and 48 hr, respectively. No significant difference was found between PIM24 hr and PIM48 hr. DeltaR1-based PIM is an accurate and reproducible method for quantifying myocardial viability distribution, and thus enhances the clinical utility of CE-MRI.
Insights
Percent infarct mapping (PIM) using longitudinal relaxation-rate enhancement (DeltaR1) accurately quantifies myocardial viability after infarction. This novel method improves cardiac magnetic resonance imaging (CE-MRI) for managing myocardial infarction (MI).
Area of Science:
- Cardiovascular Imaging
- Biomedical Engineering
- Radiology
Background:
- Myocardial infarction (MI) management requires accurate infarct size assessment.
- Current signal intensity (SI)-based MRI methods may overestimate infarct size.
- Longitudinal relaxation-rate enhancement (DeltaR1) offers an intrinsic parameter for precise quantification.
Purpose of the Study:
- To introduce and validate a DeltaR1-based contrast-enhanced MRI (CE-MRI) method called percent infarct mapping (PIM).
- To quantify myocardial viability and infarct size following delayed persistent contrast agent (PCA) accumulation.
- To assess the accuracy and reproducibility of PIM compared to histochemistry.
Main Methods:
- Developed a DeltaR1-based PIM method for CE-MRI.
- Utilized a canine MI model (N=6) with a persistent contrast agent (PCA).
- Generated voxel-by-voxel R1 maps and calculated PI values at 24 and 48 hours post-PCA administration, validated with triphenyltetrazolium-chloride (TTC) histochemistry.
Main Results:
- PIM demonstrated significant correlations (P<0.01, R=0.97) with TTC-based infarct size measurements.
- Median deviations of PIM from TTC were minimal (1.01% at 24 hr, -0.53% at 48 hr).
- Median deviations from the true infarction fraction were low (1.23% at 24 hr, 0.49% at 48 hr), with no significant difference between 24 and 48 hr PIM.
Conclusions:
- DeltaR1-based PIM is an accurate and reproducible method for quantifying myocardial viability distribution.
- PIM enhances the clinical utility of CE-MRI for myocardial infarction assessment.
- This technique provides precise per-voxel percentage of infarcted tissue, improving patient management.
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