Skip to main navigation Skip to search Skip to main content

Prediction of the development of new coronary atherosclerotic plaques with radiomics

  • Sang Eun Lee
  • , Youngtaek Hong
  • , Jongsoo Hong
  • , Juyeong Jung
  • , Ji Min Sung
  • , Daniele Andreini
  • , Mouaz H. Al-Mallah
  • , Matthew J. Budoff
  • , Filippo Cademartiri
  • , Kavitha Chinnaiyan
  • , Jung Hyun Choi
  • , Eun Ju Chun
  • , Edoardo Conte
  • , Ilan Gottlieb
  • , Martin Hadamitzky
  • , Yong Jin Kim
  • , Byoung Kwon Lee
  • , Jonathon A. Leipsic
  • , Erica Maffei
  • , Hugo Marques
  • Pedro de Araújo Gonçalves, Gianluca Pontone, Sanghoon Shin, Peter H. Stone, Habib Samady, Renu Virmani, Jagat Narula, Leslee J. Shaw, Jeroen J. Bax, Fay Y. Lin, James K. Min, Hyuk Jae Chang
  • Ewha Womans University
  • Yonsei University
  • IRCCS Istituto Ortopedico Galeazzi - Milano
  • University of Milan
  • Houston Methodist
  • The Lundquist Institute
  • Fondazione Monasterio
  • William Beaumont Hospital
  • Pusan National University
  • Seoul National University
  • IRCCS Centro Cardiologico S.P.A. Fondazione Monzino - Milano
  • Casa de Saude São Jose
  • Technical University of Munich
  • University of British Columbia
  • IRCCS SDN Istituto di Ricerca Diagnostica e Nucleare - Napoli
  • Hospital da Luz
  • Brigham and Women’s Hospital
  • Northeast Georgia Health System
  • CVPath Institute, Inc.
  • University of Texas Health Science Center at Houston
  • Icahn School of Medicine at Mount Sinai
  • Leiden University
  • Cleerly, Inc.

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Background: Radiomics is expected to identify imaging features beyond the human eye. We investigated whether radiomics can identify coronary segments that will develop new atherosclerotic plaques on coronary computed tomography angiography (CCTA). Methods: From a prospective multinational registry of patients with serial CCTA studies at ≥ 2-year intervals, segments without identifiable coronary plaque at baseline were selected and radiomic features were extracted. Cox models using clinical risk factors (Model 1), radiomic features (Model 2) and both clinical risk factors and radiomic features (Model 3) were constructed to predict the development of a coronary plaque, defined as total PV ​≥ ​1 ​mm3, at follow-up CCTA in each segment. Results: In total, 9583 normal coronary segments were identified from 1162 patients (60.3 ​± ​9.2 years, 55.7% male) and divided 8:2 into training and test sets. At follow-up CCTA, 9.8% of the segments developed new coronary plaque. The predictive power of Models 1 and 2 was not different in both the training and test sets (C-index [95% confidence interval (CI)] of Model 1 vs. Model 2: 0.701 [0.690–0.712] vs. 0.699 [0.0.688–0.710] and 0.696 [0.671–0.725] vs. 0.0.691 [0.667–0.715], respectively, all p ​> ​0.05). The addition of radiomic features to clinical risk factors improved the predictive power of the Cox model in both the training and test sets (C-index [95% CI] of Model 3: 0.772 [0.762–0.781] and 0.767 [0.751–0.787], respectively, all p ​< ​00.0001 compared to Models 1 and 2). Conclusion: Radiomic features can improve the identification of segments that would develop new coronary atherosclerotic plaque. Clinical Trial Registration: ClinicalTrials.gov NCT0280341.

Original languageEnglish
Pages (from-to)274-280
Number of pages7
JournalJournal of Cardiovascular Computed Tomography
Volume18
Issue number3
DOIs
StatePublished - 1 May 2024

Keywords

  • Coronary artery atherosclerosis
  • Coronary artery disease
  • Coronary computed tomography angiography
  • Radiomics

Fingerprint

Dive into the research topics of 'Prediction of the development of new coronary atherosclerotic plaques with radiomics'. Together they form a unique fingerprint.

Cite this