Development of physiologically-informed computational coronary artery plaques for use in virtual imaging trials
Thomas J Sauer1, Andrew J Buckler2, Ehsan Abadi1
1Center for Virtual Imaging Trials, Carl E. Ravin Advanced Imaging Laboratories, Department of Radiology, the Duke University Medical Center, Durham, North Carolina, USA.
Medical Physics
|February 2, 2024
Summary
Researchers developed realistic coronary plaque models using deep learning for virtual imaging trials. These models enable quantitative evaluation and optimization of cardiac imaging technologies, offering a faster and more cost-effective alternative to traditional clinical trials for cardiovascular disease.
Area of Science:
- Biomedical imaging
- Computational modeling
- Cardiovascular disease research
Background:
- Cardiovascular disease (CVD) is a leading global cause of death, with coronary artery disease (CAD) being a major contributor.
- Traditional clinical trials for validating cardiac imaging technologies are time-consuming, expensive, and require large patient cohorts.
- Virtual imaging trials (VITs) offer a promising alternative by using virtual patients and accurate imaging device models.
Purpose of the Study:
- To develop physiologically-informed, realistic coronary plaque models for cardiac imaging VITs.
- To create anatomically variable plaque models with clinical realism for simulation purposes.
Main Methods:
- A deep convolutional generative adversarial network (DC-GAN) was trained on high-resolution histology images to generate plaque models.
- Finite element analysis (FEA) was used to assess the stability of the generated plaque models under physiological conditions.
- The plaque models were integrated with the XCAT computational phantom for simulations comparing energy-integrating detector (EID) CT and photon-counting detector (PCD) CT.
Main Results:
- The DC-GAN successfully generated realistic and anatomically diverse coronary plaque models.
- Simulation results demonstrated the utility of these models for comparing different cardiac imaging devices.
Conclusions:
- Generated CAD pathologies can be incorporated into computational phantoms for VITs.
- These models provide a "known truth" for quantitative optimization and evaluation of cardiac imaging technologies.


