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Myocardial Infarction and Functional Outcome Assessment in Pigs
Published on: April 25, 2014
Impact of Subtended Myocardial Mass Assessed by Coronary Computed Tomographic Angiography-Based Myocardial
Soo-Jin Kang1, Young-Hak Kim1, June-Goo Lee2
1Department of Cardiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
Insights
Coronary artery-based myocardial segmentation (CAMS) can predict major adverse cardiac events (MACE) in untreated coronary lesions. This method enhances the identification of ischemia-producing lesions, improving clinical decision-making for revascularization.
Area of Science:
- Cardiology
- Medical Imaging
- Interventional Cardiology
Background:
- Revascularization decisions typically rely on ischemic myocardium extent.
- The prognostic significance of myocardial territories supplied by coronary arteries remains understudied.
Purpose of the Study:
- To assess the clinical impact of coronary artery-based myocardial segmentation (CAMS)-derived myocardial volume subtended to poststenotic segments.
- To identify clinically relevant coronary lesions using CAMS and fractional flow reserve (FFR).
Main Methods:
- Analysis of coronary computed tomography angiography, invasive coronary angiography, and FFR data from 664 deferred and 401 treated lesions.
- Calculation of myocardial volume subtended to stenotic segments (Vsub) using the CAMS method.
- Evaluation of 3-year target vessel-related major adverse cardiac event (MACE) including cardiac death, myocardial infarction, and target vessel revascularization.
Main Results:
- Vsub, FFR, and distal reference luminal diameter independently predicted 3-year MACE in deferred lesions.
- A Vsub ≥ 36.2cc predicted MACE in deferred lesions with 72% sensitivity and 67% specificity (AUC 0.71).
- CAMS-derived Vsub improved the diagnostic performance of angiography for identifying ischemia-producing lesions compared to diameter stenosis and minimal luminal diameter.
Conclusions:
- CAMS-derived Vsub is a valuable predictor of 3-year clinical outcomes in untreated coronary lesions.
- Vsub enhances the ability to identify ischemia-producing lesions, aiding in revascularization decisions.
- This approach offers prognostic information beyond traditional angiographic parameters.
Abstract:
Although decision-making for revascularization is based on the extent of ischemic myocardium, the prognostic implication of supplying myocardial territories has not yet been studied. To evaluate the clinical impact of the coronary artery-based myocardial segmentation (CAMS)-derived myocardial volume subtended to the poststenotic segment, and to determine clinically relevant coronary lesions, coronary computed tomography angiography, invasive coronary angiography, and preprocedure fractional flow reserve (FFR) data were analyzed in 664 deferred lesions (in 577 patients) and 401 treated lesions (in 369 patients) with drug-eluting stent implantation, respectively. Using CAMS method, the myocardial volume subtended to a stenotic coronary segment (Vsub) was assessed. The primary composites included target vessel-related major adverse cardiac event (MACE) including cardiac death, myocardial infarction, and target vessel revascularization over 3 years. Independent predictors of 3-year MACE in deferred lesions were Vsub (adjusted hazard ratio [HR] 1.02), FFR (adjusted HR per 0.1 = 0.60), and distal reference luminal diameter (adjusted HR 2.04, all p < 0.05). A Vsub ≥ 36.2cc was predictive of MACE in deferred lesions with a sensitivity 72% and a specificity 67% (area under curve 0.71, 95% confidence interval 0.67 to 0.74, p < 0.001). Vsub was not associated with target vessel-related MACE. For the prediction of FFR < 0.80, the area under curve of Vsub/MLD4 > 6.3 was greater than those of angiographic diameter stenosis (0.78 vs 0.69) and minimal luminal diameter (0.78 vs 0.71), (all p < 0.05). CAMS-derived Vsub predicted 3-year clinical outcomes in untreated coronary lesions, and improved the diagnostic performance of angiography-derived parameters to identify ischemia-producing lesions.
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