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AI-Guided Quantitative Plaque Staging Predicts Long-Term Cardiovascular Outcomes in Patients at Risk for ASCVD
summary
This abstract is available on the publisher's site.
Access this abstract now Full Text Available for ClinicalKey SubscribersBACKGROUND
The recent development of artificial intelligence-guided quantitative coronary computed tomography angiography (CCTA) analysis (AI-QCT) has enabled rapid analysis of atherosclerotic plaque burden and characteristics.
OBJECTIVES
This study set out to investigate the 10-year prognostic value of atherosclerotic burden derived from AI-QCT and to compare the spectrum of plaque to manually assessed CCTA, coronary artery calcium scoring (CACS), and clinical risk characteristics.
METHODS
This was a long-term follow-up study of 536 patients referred for suspected coronary artery disease. CCTA scans were analyzed with AI-QCT and plaque burden was classified with a plaque staging system (stage 0: 0% percentage atheroma volume [PAV]; stage 1: >0%-5% PAV; stage 2: >5%-15% PAV; stage 3: >15% PAV). The primary major adverse cardiac event (MACE) outcome was a composite of nonfatal myocardial infarction, nonfatal stroke, coronary revascularization, and all-cause mortality.
RESULTS
The mean age at baseline was 58.6 years and 297 patients (55%) were male. During a median follow-up of 10.3 (IQR: 8.6-11.5) years, 114 patients (21%) experienced the primary outcome. Compared to stages 0 and 1, patients with stage 3 PAV and percentage of noncalcified plaque volume of >7.5% had a more than 3-fold (adjusted HR: 3.57; 95% CI 2.12-6.00; P < 0.001) and 4-fold (adjusted HR: 4.37; 95% CI: 2.51-7.62; P < 0.001) increased risk of MACE, respectively. Addition of AI-QCT improved a model with clinical risk factors and CACS at different time points during follow-up (10-year AUC: 0.82 [95% CI: 0.78-0.87] vs 0.73 [95% CI: 0.68-0.79]; P < 0.001; net reclassification improvement: 0.21 [95% CI: 0.09-0.38]). Furthermore, AI-QCT achieved an improved area under the curve compared to Coronary Artery Disease Reporting and Data System 2.0 (10-year AUC: 0.78; 95% CI: 0.73-0.83; P = 0.023) and manual QCT (10-year AUC: 0.78; 95% CI: 0.73-0.83; P = 0.040), although net reclassification improvement was modest (0.09 [95% CI: -0.02 to 0.29] and 0.04 [95% CI: -0.05 to 0.27], respectively).
CONCLUSIONS
Through 10-year follow-up, AI-QCT plaque staging showed important prognostic value for MACE and showed additional discriminatory value over clinical risk factors, CACS, and manual guideline-recommended CCTA assessment.
Additional Info
Disclosure statements are available on the authors' profiles:
AI-Guided Quantitative Plaque Staging Predicts Long-Term Cardiovascular Outcomes in Patients at Risk for Atherosclerotic CVD
JACC Cardiovasc Imaging 2023 Jul 07;[EPub Ahead of Print], NS Nurmohamed, MJ Bom, RA Jukema, RJ de Groot, RS Driessen, PA van Diemen, RW de Winter, EL Gaillard, RW Sprengers, ESG Stroes, JK Min, JP Earls, R Cardoso, R Blankstein, I Danad, AD Choi, P KnaapenFrom MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
The increasing use of AI has extended to reading CCTA results, now referred to as AI-guided quantitative analysis (AI-QCT). This now enables rapid analysis of atherosclerotic plaque burden and characteristics. The ability to incorporate plaque burden, types of plaque (ie, vulnerable plaque volume), high-risk plaque features (ie, remodeling and spotty calcification), and location/severity of stenosis will undoubtedly provide clinicians with more information than coronary calcium scoring (CCS) or simple interpretation of stenosis severity based on the Coronary Artery Disease Reporting and Data System 2.0 (CAD-RADS 2.0).
The current study used stored scans from a decade earlier to evaluate the incremental prognostic value of AI-QCT compared with CCS, clinical risk factors, and CAD RADS 2.0. Not surprising, AI-QCT improved a model with clinical risk factors and CCS at 10-year follow-up. Perhaps surprising, there was little incremental value to knowing maximum stenosis severity, with net reclassification improvement being modest (CAD-RADS 2.0, 0.090 [95% CI, −0.02 to 0.29]; and manual QCT, 0.04 [95% CI, −0.05 to 0.27]).
It is likely that, as we learn more about plaque, location, and remodeling, AI can continue to improve risk prediction. It already affords the only practical way to measure plaque burden over time clinically for CCTA, as manual or semi-automated methods take up to 1 hour to perform. The time for AI-QCT is measured in minutes and, as computing gets better, may continue to improve. Thus, patients can get baseline CCTA and have plaque, stenosis, and high-risk features measured by AI-QCT and then follow-up in 1 to 2 years for a repeat test, evaluating whether atherosclerosis has progressed and if high-risk features have developed or resolved over time.
One must remember that it is possible to optimize the AI programs for any given dataset, so prospective evaluation of this performance is necessary. Despite this, we have entered the age of AI in cardiac imaging, which will lead to less reading time, faster and more accurate risk assessment, and the ability to combine multiple different metrics on CCTA to predict events and track atherosclerosis. The role of the expert reader and how they he/she interacts with these interpretations still needs to be worked out as well, both from a liability and work-flow perspective.
Development of these AI programs are just in the infancy, as there are literally thousands of "-omics" available on any given CT scan, involving location (ie, left main vs distal right coronary), plaque assessment (CCS, plaque volume, and type), stenosis severity and location, and eventually other metrics of risk on the scan, such as pericoronary fat attenuation, epicardial (visceral) fat, bone density, aortic atherosclerosis, and valve calcifications.