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Updated: Mar 8, 2026

In Vivo Quantitative Assessment of Myocardial Structure, Function, Perfusion and Viability Using Cardiac Micro-computed Tomography
Published on: February 16, 2016
Non-contrast multimodal cardiac MRI for predicting coronary microvascular dysfunction in patients with hypertrophic
Jiaqi Li1, Lingcheng Zhu2, Yangyingqiu Liu2
1School of Medical Imaging, Binzhou Medical University, Guanhai Street No. 346, Laishan District, Yantai 264003, Shandong Province, China.
Insights
A novel non-contrast radiomics model effectively identifies coronary microcirculatory dysfunction (CMD) in hypertrophic cardiomyopathy (HCM) patients. This approach using T1 mapping shows promise for reducing contrast agent use in cardiac magnetic resonance (CMR) imaging.
Area of Science:
- Cardiology
- Medical Imaging
- Artificial Intelligence
Background:
- Coronary microcirculatory dysfunction (CMD) is a key feature in hypertrophic cardiomyopathy (HCM).
- Current detection methods often rely on contrast-enhanced cardiac magnetic resonance (CMR), which carries risks associated with contrast agents.
- There is a need for non-invasive and contrast-agent-sparing techniques for CMD assessment in HCM.
Purpose of the Study:
- To develop and validate a practical non-contrast radiomics model for identifying CMD in HCM patients.
- To minimize the reliance on contrast agents in the diagnostic workflow.
- To assess the diagnostic performance and clinical utility of the developed model.
Main Methods:
- A cohort of 290 HCM patients was divided into training (80%) and testing (20%) sets.
- Radiomics features were extracted from cine, T1 mapping, and T2 fat-saturation CMR images.
- Five machine learning algorithms were used to build radiomics models, with ensemble models also generated.
Main Results:
- The SF2 model, incorporating T1 mapping features, demonstrated the highest diagnostic performance.
- The SF2 model achieved an AUC of 0.90, accuracy of 0.83, sensitivity of 0.87, and specificity of 0.75 in the test set.
- Calibration and decision curve analyses confirmed the model's good calibration and superior clinical utility.
Conclusions:
- The non-contrast SF2 radiomics model effectively detects CMD in HCM patients.
- This radiomics approach offers a promising alternative to contrast-enhanced CMR.
- The findings suggest a potential reduction in contrast agent utilization for CMD assessment.
Objective:
In hypertrophic cardiomyopathy (HCM), detection of coronary microcirculatory dysfunction (CMD) usually relies on contrast-enhanced cardiac magnetic resonance (CMR). This study sought to develop a practical non-contrast radiomics model to identify CMD, minimizing reliance on contrast agents.
Methods:
A total of 290 patients with HCM were stratified by the presence or absence of CMD and randomly allocated into a training set and a test set at an 8:2 ratio. The application of logistic regression was implemented to identify predictive imaging features. Radiomics features were extracted from the end-diastolic four-chamber view of the left ventricle and the end-diastolic short-axis view with maximal wall thickness across cine, T1 mapping, and T2 fat-saturation images. Five distinct machine learning algorithms were then employed to construct radiomics models, and ensemble models were generated by integrating features from different imaging planes. Model performance was evaluated in the test set using receiver operating characteristic (ROC) analysis, calibration curves, and decision curve analysis (DCA).
Results:
Random forest (RF) outperformed other machine learning algorithms. Nine predictive models were constructed: S1(SAX-CINE-clinical model), F1(4CH-CINE-clinical model), and SF1 (SAX-4CH-CINE-clinical model); S2(SAX-T1 mapping-clinical model), F2(4CH-T1 mapping-clinical model), and SF2 (SAX-4CH-T1 mapping-clinical model); and S3(SAX-T2FS-clinical model), F3(4CH-T2FS-clinical model), and SF3 (SAX-4CH-T2FS-clinical model). In the test set, the SF2 model showed the best diagnostic performance, achieving an AUC of 0.90, accuracy of 0.83, sensitivity of 0.87, specificity of 0.75, and an F1 score of 0.87 for detecting coronary microcirculatory dysfunction. Calibration and decision curve analyses further demonstrated that SF2 was well-calibrated and offered superior clinical utility.
Conclusion:
The SF2 radiomics model, integrating T1 mapping features, demonstrated the best diagnostic performance for detecting CMD in HCM patients. These findings indicate that non-contrast radiomics holds promise as a potential alternative to contrast-enhanced CMR, with the capacity to reduce reliance on contrast agents in CMD assessment.
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