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Juhwan Lee, Ph.D.

Assistant Professor, Department of Biomedical Engineering VCU College of Engineering

  • Richmond VA

Dr. Juhwan Lee’s research focuses on artificial intelligence, medical image analysis, and their applications in cardiovascular medicine.

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Biography

I am an Assistant Professor of Biomedical Engineering at VCU with significant experience in medical image processing, machine/deep learning, and their clinical applications. My research focuses on developing AI methods for intravascular imaging, coronary computed tomography angiography, coronary artery calcium scoring, and chest X-ray analysis to predict short- and long-term cardiovascular outcomes. As a translational scientist, I have more than a decade of experience conducting interdisciplinary research that helps cardiologists and radiologists make more informed treatment decisions. Currently, I serve as Principal Investigator on multiple NIH-funded projects. My long-term goal is to develop interpretable AI models that improve personalized cardiovascular care and patient outcomes.

Industry Expertise

Medical Devices

Areas of Expertise

Cardiology
Artificial Intelligence
Machine Learning & Deep Learning
Medical Image Analysis

Education

Case Western Reserve University

Postdoctoral fellowship

Biomedical Engineering

2020

Dongguk University

Ph.D.

Biomedical Engineering

2015

Patents

Prediction of major adverse cardiovascular events (mace) from ai analysis of pericoronary fat in ct images

US12573036B2

2026-03-10

The present disclosure, in some embodiments, relates to a method of generating a prognosis for a patient. The method includes accessing automatically segmented pericoronary adipose tissue (PCAT) corresponding to a patient within an electronic memory. A plurality of non-confounding PCAT features are generated by measuring values of Hounsfield units for an imaging unit within the PCAT. The measured values of the Hounsfield units are predominately free of iodine confounding and artifacts. The plurality of non-confounding PCAT features are provided to a regression model. The regression model is configured to generate a prognosis for the patient using the plurality of non-confounding PCAT features

Plaque segmentation in intravascular optical coherence tomography (OCT) images using deep learning

US11710238B2

2023-07-25

Embodiments discussed herein facilitate segmentation of vascular plaque, training a deep learning model to segment vascular plaque, and/or informing clinical decision-making based on segmented vascular plaque. One example embodiment accessing vascular imaging data for a patient, wherein the vascular imaging data comprises a volume of interest; pre-process the vascular imaging data to generate pre-processed vascular imaging data; provide the pre-processed vascular imaging data to a deep learning model trained to segment a lumen and a vascular plaque; and obtain segmented vascular imaging data from the deep learning model, wherein the segmented vascular imaging data comprises a segmented lumen and a segmented vascular plaque in the volume of interest.

Research Grants

Cardiovascular risk prediction from AI analysis of coronary calcifications

NIH STTR

2025-08-15

We will create software for predicting cardiovascular health from a low-cost (no-cost) CT calcium score examination, which shows calcifications in the coronary arteries. We will use artificial intelligence to greatly improve the existing CT calcium score method, creating a method that physicians and patients can use in shared decision-making to personalize interventions.

Multi-modality evaluation of high-risk coronary atherosclerotic plaque

NIH K01

2024-09-01

We will develop methods for the non-invasive, quantitative evaluation of coronary artery disease in computed tomography angiography images. With success, our research will lead to improved detection of coronary artery disease and evaluation of its severity, paving the way for personalized treatments.

Selected Articles

Sub-Agatston coronary calcification on non-contrast cardiac CT and cardiovascular risk Get access Arrow

European Journal of Preventive Cardiology

Prerna Singh, Ammar Hoori, Juhwan Lee, Michelle C Williams, Sadeer Al-Kindi, David E Newby, Sanjay Rajagopalan, David L Wilson

2026-06-01

Aims
To develop assessments of low-density (‘sub-Agatston’) coronary artery calcification (CAC) on non-contrast CT calcium score (CTCS) examinations to evaluate its association with the risk of atherosclerotic major adverse cardiac events (MACE) and with high-risk plaque (HRP) features from coronary CT angiography (CCTA).

Methods and results
We analysed 1837 asymptomatic individuals from the Community Benefit of No-charge Calcium Score Screening (CLARIFY) CTCS registry (NCT04075162) and 1075 patients presenting at chest-pain clinics from the Scottish COmputed Tomography of the HEART (SCOT-HEART) trial (NCT01149590). MACE comprised death, myocardial infarction, stroke, or revascularization. We developed the vulnerable calcium index (VCI), which quantifies the proportional CAC mass increase after region-growing from 130 Hounsfield Units (HU) (Agatston) to 110 HU. Cox models were adjusted for age, sex, diabetes, hypertension, smoking, baseline statin use, and Agatston score. The association between VCI and CCTA-defined HRP (low-attenuation plaque, positive remodelling, spotty calcifications, mixed plaque, punctate calcification, napkin-ring sign) was assessed in patients with paired CTCS and CCTA in SCOT-HEART. Median follow-up was 4.8 years (CLARIFY) and 4.9 years (SCOT-HEART). VCI was independently associated with MACE in both cohorts: CLARIFY (adjusted hazard ratio [HR] 1.12, 95% confidence interval [CI] 1.02–1.22, P = 0.02) per unit increase in VCI and SCOT-HEART (adjusted HR 1.16, 1.03–1.31, P = 0.02). Patients in the top quartile of adjusted model risk had markedly higher event rates compared with the lowest quartile (CLARIFY HR 25.0; SCOT-HEART HR 33.7 vs. Q1, P < 0.005 for both). Addition of VCI to Agatston significantly improved C-index (CLARIFY: 0.62 to 0.66, P < 0.001; SCOT-HEART: 0.72 to 0.75, P < 0.001) and net reclassification index (CLARIFY: 0.52 [0.40, 0.64], P < 0.005; SCOT-HEART: 0.72 [0.48, 0.94], P < 0.005). In SCOT-HEART, VCI was associated with all HRP features (odds ratio: 1.45–1.85, P < 0.001), adjusted for Agatston score.

Conclusion
VCI captures sub-Agatston CAC linked to HRP and independently improves MACE prediction in both a primary-prevention and a mixed-risk symptomatic chest pain population. Incorporating VCI into CAC reporting may refine preventive risk stratification beyond the conventional Agatston score.

Hybrid deep learning time-to-event modeling of major adverse cardiovascular events using coronary artery calcium score scans

European Journal of Radiology Artificla Intelligence

Justin N Kim, Juhwan Lee, Ammar Hoori, Hao Wu, Tao Hu, Sadeer Al-Kindi, Mohamed Makhlouf, Robert Gilkeson, Sanjay Rajagopalan, David L Wilson

2026-09-07

Background
The Agatston score from non-contrast coronary calcium scoring scan (CACS) is a robust predictor of major adverse cardiovascular events (MACE) but summarizes total calcium burden and may miss other risk-related imaging information in CACS. We hypothesized that a hybrid deep-learning (DL) model integrating image features with clinical, Agatston, and calcium-omics data could improve MACE risk prediction.
Methods
In this retrospective cohort of 1950 patients, a DenseNet-121 encoder extracted DL-derived features from CACS volume, which were fused with tabular data (clinical features, Agatston, and 15 calcium-omics features) within a deep survival model. Performance was assessed via five-fold cross-validation using Harrell’s concordance-index (C-index) and time-dependent area under the curve (AUC), and net reclassification index (NRI), relative to tabular-only baseline.
Results
Expanding the tabular feature set from clinical variables alone to include Agatston and calcium-omics improved discrimination for both tabular-only baseline and hybrid models. Incorporating DL-derived imaging representations consistently outperformed tabular baselines in C-indices (0.802 vs. 0.789 with the full feature set) and yielded higher time-dependent AUCs during first three years of follow-up. The hybrid model also achieved an NRI of 0.119 (p = 0.037). Patients reclassified from low to high risk had a significantly higher event rate (37.5%) compared to those remaining low risk (1.1%, p 

Pericoronary adipose tissue feature analysis in computed tomography calcium score images in comparison to coronary computed tomography angiography

Journal of Medical Imaging

Yingnan Song, Hao Wu, Juhwan Lee, Justin Kim, Ammar Hoori, Tao Hu, Vladislav Zimin, Mohamed Makhlouf, Sadeer Al-Kindi, Sanjay Rajagopalan, Chun-Ho Yun, Chung-Lieh Hung, David L Wilson

2025-01-12

Purpose: We investigated the feasibility and advantages of using non-contrast CT calcium score (CTCS) images to assess pericoronary adipose tissue (PCAT) and its association with major adverse cardiovascular events (MACE). PCAT features from coronary computed tomography angiography (CCTA) have been shown to be associated with cardiovascular risk but are potentially confounded by iodine. If PCAT in CTCS images can be similarly analyzed, it would avoid this issue and enable its inclusion in formal risk assessment from readily available, low-cost CTCS images.

Approach: To identify coronaries in CTCS images that have subtle visual evidence of vessels, we registered CTCS with paired CCTA images having coronary labels. We developed an "axial-disk" method giving regions for analyzing PCAT features in three main coronary arteries. We analyzed hand-crafted and radiomic features using univariate and multivariate logistic regression prediction of MACE and compared results against those from CCTA.

Results: Registration accuracy was sufficient to enable the identification of PCAT regions in CTCS images. Motion or beam hardening artifacts were often prevalent in "high-contrast" CCTA but not CTCS. Mean HU and volume were increased in both CTCS and CCTA for the MACE group. There were significant positive correlations between some CTCS and CCTA features, suggesting that similar characteristics were obtained. Using hand-crafted/radiomics from CTCS and CCTA, AUCs were 0.83/0.79 and 0.83/0.77, respectively, whereas Agatston gave AUC = 0.73.

Conclusions: Preliminarily, PCAT features can be assessed from three main coronary arteries in non-contrast CTCS images with performance characteristics that are at the very least comparable to CCTA.