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AI-Quantitative CT Coronary Plaque Features Associate With a Higher Relative Risk in Women: CONFIRM2 Registry

  • Gudrun M. Feuchtner
  • , Pietro G. Lacaita
  • , Jeroen J. Bax
  • , Fatima Rodriguez
  • , Rine Nakanishi
  • , Gianluca Pontone
  • , Saima Mushtaq
  • , Ronny R. Buechel
  • , Christoph Gräni
  • , Amit R. Patel
  • , Cristiane C. Singulane
  • , Andrew D. Choi
  • , Mouaz Al-Mallah
  • , Daniele Andreini
  • , Ronald P. Karlsberg
  • , Geoffrey Cho
  • , Carlos E. Rochitte
  • , Mirvat Alasnag
  • , Ashraf Hamdan
  • , Filippo Cademartiri
  • Erica Maffei, Hugo Marques, Pedro M. Gonçalves Pereira, Himanshu Gupta, Martin Hadamitzky, Omar Khalique, Dinesh Kalra, James D. Mills, Nick S. Nurmohamed, Paul Knaapen, Matthew Budoff, Kashif Shaikh, Enrico Martin, David M. German, Maros Ferencik, Andrew C. Oehler, Roderick Deaño, Prashant Nagpal, Marly Van Assen, Carlo Nicola De Cecco, Borek Foldyna, Jan Michael Brendel, Victor Y. Cheng, Kelley Branch, Marcio Bittencourt, Sabha Bhatti, Venkateshwar Polsani, George Wesbey, Rhanderson Cardoso, Ron Blankstein, Augustin Delago, Amit Pursnani, Amro Alsaid, Stephen Bloom, Vasileios Kamperidis, Fabian Barbieri, Melissa Aquino, Ibrahim Danad, Alexander van Rosendael
  • Medizinische Universität Innsbruck
  • Leiden University Medical Centre
  • Stanford University School of Medicine
  • Toho University Graduate School of Medicine
  • Istituto di Ricovero e Cura A Carattere Scientifico (IRCCS)
  • University of Milan
  • University Children's Hospital Zurich
  • Inselspital Universitatsspital
  • University of Virginia
  • George Washington University and Complex Systems Institute
  • Methodist Neurological Institute
  • David Geffen School of Medicine at UCLA
  • University of São Paulo
  • King Fahd Armed Forces Hospital
  • Tel Aviv University
  • IRCCS SDN
  • Hospital da Luz
  • Heart and Vascular Institute of New Jersey
  • St. Francis Hospital - The Heart Center
  • University of Louisville School of Medicine
  • West Virginia University School of Medicine Morgantown
  • VU University Amsterdam
  • Department of Pediatrics
  • University of Tennessee Medical Center
  • MercyOne-Iowa Heart Center
  • Oregon Health and Science University
  • Allegheny Health Network
  • University of Wisconsin School of Medicine and Public Health
  • Emory University School of Medicine
  • Harvard Medical School
  • Minneapolis Heart Institute
  • University of Washington School of Medicine
  • University of Pittsburgh
  • National Institute of Cardiovascular Diseases Pakistan
  • Piedmont Heart Institute
  • Scripps Clinic
  • Brigham and Women's Hospital
  • Medical Data Research Collaborative
  • Endeavor NorthShore Cardiovascular Institute
  • Pritzker School of Medicine
  • Scott and White
  • Midwest Heart and Vascular Associates
  • Aristotle University of Thessaloniki
  • German Heart Institute Berlin
  • Cleerly Healthcare
  • Amalia Children's Hospital

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

BACKGROUND: Coronary plaque features are imaging biomarkers of cardiovascular risk, but less is known about sex-specific patterns in their prognostic value. This study aimed to define sex differences in the coronary atherosclerotic phenotypes assessed by artificial intelligence–based quantitative computed tomography (AI-QCT) and the associated risk of major adverse cardiovascular events (MACEs). METHODS: Global multicenter registry including symptomatic patients with suspicion of coronary artery disease referred for coronary computed tomography angiography. AI-QCT analyzed 16 coronary artery disease features. The primary end point was MACE defined as death, myocardial infarction, late revascularization, cerebrovascular events, unstable angina, and congestive heart failure. RESULTS: Among 3551 patients (mean age, 59±12 years; 49.5% women), MACE occurred in 3.2% of women and 6.1% of men during an average follow-up of 4.8±2.2 years. The AI-QCT features total plaque volume, noncalcified plaque, calcified plaque, and percentage atheroma volume were significantly higher in men (P<0.001), and high-risk plaques were more prevalent (9.2% versus 2.5%; P<0.0001). Independent of age and cardiovascular risk factors, the AI-QCT-derived features of total plaque volume, noncalcified plaque, calcified plaque, and percentage atheroma volume conferred a higher relative risk of MACE in women than men. For every 50-mm3 increase in total plaque volume, relative risk increased by 17.7% (95% CI, 1.12–1.24) in women versus 5.3% (95% CI, 1.03–1.07) in men (Pinteraction<0.001); for noncalcified plaque, relative risk increased by 27.1% (95% CI, 1.17–1.38) versus 11.6% (95% CI, 1.08–1.15; Pinteraction=0.0015); and for calcified plaque, relative risk increased by 22.9% (95% CI, 1.14–1.33) versus 5.4% (95% CI, 1.01–1.10; Pinteraction=0.0012), respectively. Similarly, for percentage atheroma volume, the risk was higher in women. The findings remained unchanged when restricted to a secondary composite end point (death and myocardial infarction). CONCLUSIONS: The AI-QCT plaque features, total plaque volume, noncalcified plaque, calcified plaque, and percentage atheroma volume, conferred a higher relative MACE risk in women and may prompt more aggressive antiatherosclerotic therapy and reinforced preventive interventions.

Original languageEnglish
JournalCirculation: Cardiovascular Imaging
Volume18
Issue number6
DOIs
StatePublished - 1 Jun 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • artificial intelligence
  • atherosclerosis
  • computed tomography
  • computed tomography angiography
  • coronary artery disease
  • women’s health

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