Abstract 4369876: CT-Based Radiomics Offers Prognostic Insight in Cardiomyopathy Patients Undergoing ICD Implantation

M Maryam Mojarrad Sani (Johns Hopkins University School of Medicine, Baltimore, Maryland, United States) G Ghazal Zandieh (Johns Hopkins University School of Medicine, Baltimore, Maryland, United States) A Ashkan Abdollahi (Johns Hopkins University School of Medicine, Baltimore, Maryland, United States) M Marc Engels (Johns Hopkins University School of Medicine, Baltimore, Maryland, United States) K Katherine Wu J Joao AC Lima (JOHNS HOPKINS UNIVERSITY, Timonium, Maryland, United States) S Stefan Zimmerman (Johns Hopkins University School of Medicine, Baltimore, Maryland, United States) B Bharath Ambale-Venkatesh (Johns Hopkins University School of Medicine, Baltimore, Maryland, United States) J Jonathan Chrispin (Johns Hopkins University School of Medicine, Baltimore)

Abstract

Introduction: Intramyocardial fat and scar burden have been linked to mortality in cardiomyopathy (CM) patients. However, the prognostic value of advanced imaging features derived from cardiac CT remains underexplored. This study evaluated whether radiomic features from cardiac CT improve prediction of all-cause mortality in CM patients receiving a primary prevention implantable cardioverter-defibrillator (ICD). Methods: Patients enrolled in the PROSE-ICD study underwent cardiac CT and were followed for all-cause death. CTs were acquired on 64-slice scanners, and the left ventricle was segmented using 3D Slicer with TotalSegmentator. A total of 92 radiomic features were extracted (PyRadiomics 3.0.1) across four resampling grids (0.5–3 mm) and three bin widths (20–60 HU). The primary endpoint was all-cause mortality; ventricular arrhythmic events (n=6, 11%) were analyzed descriptively due to low counts. A clinical Cox model (age, CM etiology, diabetes) and four radiomics-based survival models were trained using 15×3-fold cross-validation. The best radiomics model (GBS, 0.5 mm grid, 20-HU bin) was combined with clinical variables in a second-stage Cox model. Model discrimination (c-index), calibration, and feature importance were assessed using Python 3.11 (lifelines, scikit-survival). Results: Among 55 patients (mean age 64 ± 9 years; 20% female; 76% White; 65.5% ischemic CM), 13 (24%) died over a median follow-up of 3,284 days (~9 years). Hypertension (89%), hyperlipidemia (95%), and diabetes (47%) were highly prevalent. Mean LVEF was 24 ± 13.7%, and 33% had a history of ventricular arrhythmia. Five-year survival was higher in non-ischemic vs. ischemic CM (89% vs. 74%, p=0.12). Diabetes was the only independent clinical predictor of mortality (HR 5.31, 95% CI 1.14–24.7, p=0.03); age and CM etiology were not significant. The clinical Cox model yielded a c-index of 0.70. The best radiomics model, based on myocardial texture heterogeneity, achieved a c-index of 0.80. Combining radiomics with clinical variables improved discrimination to 0.81 (Δ +0.02, p=0.08) with good five-year calibration (slope = 0.94). Conclusion: Radiomic features derived from high-resolution cardiac CT substantially enhance prediction of long-term mortality in cardiomyopathy patients receiving primary prevention ICDs, offering a promising non-invasive tool for personalized risk stratification.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (9)

M

Maryam Mojarrad Sani

Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

G

Ghazal Zandieh

Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

A

Ashkan Abdollahi

Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

M

Marc Engels

Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

K

Katherine Wu

J

Joao AC Lima

JOHNS HOPKINS UNIVERSITY, Timonium, Maryland, United States

S

Stefan Zimmerman

Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

B

Bharath Ambale-Venkatesh

Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

J

Jonathan Chrispin

Johns Hopkins University School of Medicine, Baltimore