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American Heart Association

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Final ID: 4335849

Improvements in Diagnostic and Therapeutic Cardiovascular Risk Assessment Through Total Plaque Volume Burden: An Analysis of the Fish&Chips Study

Abstract Body (Do not enter title and authors here): Background:
Quantitative coronary plaque analysis from coronary computed tomographic angiography (CCTA) is a promising strategy for individualized cardiovascular disease (CVD) prevention. More population-level data is needed on how plaque burden can inform lipid lowering strategies to reduce CVD risk reduction.

Objectives:
To evaluate the prognostic utility of a total plaque volume (TPV)-based risk staging system and model its use in guiding lipid-lowering therapy in real-world patients undergoing clinically indicated CCTAs for evaluation of chest pain.

Methods:
We analyzed adult patients across a single-center NHS site who underwent clinically indicated CCTA with available AI-based quantitative plaque analysis. TPV was categorized into four risk stages (DECIDE 1–4) using predefined thresholds (Table 1). The primary outcome was cardiac death or non-fatal MI. Secondary analyses reclassified prior myocardial infarction (MI) or early revascularization into DECIDE Stage 4. We modeled lipid-lowering strategies using both fixed-intensity treatment by DECIDE stage and stage-specific LDL-C goals to estimate risk reduction and number needed to treat (NNT) over 3-to-10-year durations.

Results:
Among the 2,827 patients, mean (SD) age was 58 (13) years, and 51.1% were female. Higher TPV stages were associated with progressively increased risk of CV death or MI (1.7%, 4.9%, 7.4%, 11.1% for stages 1–4, respectively) (Figure 1). The fixed intensity strategy yielded a 10-year NNT of 52, which improved to 42 when using a stage-specific LDL-C goal strategy guided by plaque burden.

Conclusions:
Quantitative plaque burden measured by AI-enabled CCTA identifies patients at elevated long-term cardiovascular risk and may inform a personalized lipid-lowering strategy to mitigate risk.
  • Parsa, Shyon  ( Stanford University Hospital , Stanford , California , United States )
  • Peng, Allison  ( Johns Hopkins School of Medicine , Baltimore , Maryland , United States )
  • Fairbairn, Timothy  ( Liverpool Heart and Chest Hospital , Liverpool , United Kingdom )
  • Bell, Jack  ( Liverpool Heart and Chest Hospital , Liverpool , United Kingdom )
  • Sengupta, Souma  ( Heartflow , San Carlos , California , United States )
  • Mullen, Sarah  ( Heartflow , San Carlos , California , United States )
  • Rogers, Campbell  ( HeartFlow , Westwood , California , United States )
  • Martin, Seth  ( Johns Hopkins School of Medicine , Baltimore , Maryland , United States )
  • Rodriguez, Fatima  ( Stanford University Hospital , Stanford , California , United States )
  • Author Disclosures:
    Shyon Parsa: DO NOT have relevant financial relationships | Allison Peng: DO NOT have relevant financial relationships | Timothy Fairbairn: No Answer | Jack Bell: No Answer | Souma Sengupta: DO have relevant financial relationships ; Employee:Heartflow:Active (exists now) | Sarah Mullen: DO have relevant financial relationships ; Employee:Heartflow:Active (exists now) | Campbell Rogers: DO have relevant financial relationships ; Employee:Heartflow:Active (exists now) ; Individual Stocks/Stock Options:Heartflow:Active (exists now) ; Executive Role:Heartflow:Active (exists now) | Seth Martin: DO have relevant financial relationships ; Consultant:Amgen, Arrowhead Pharmaceuticals, AstraZeneca, Care Access, Chroma, Bristol Myers Squibb, Heartflow, Kaneka, Merck, NewAmsterdam Pharma, Novartis, Novo Nordisk, Premier, Sanofi, Verve Therapeutics, :Past (completed) ; Ownership Interest:Corrie Health, Prevent Medical:Active (exists now) ; Other (please indicate in the box next to the company name):American Heart Association (Immediate Past Chair, EPI Statistics Committee):Active (exists now) ; Other (please indicate in the box next to the company name):National Lipid Association (SELA President):Active (exists now) ; Other (please indicate in the box next to the company name):Editorial Board Member (AJPC, EJPC, JCL):Active (exists now) ; Research Funding (PI or named investigator):National Institutes of Health, Patient-Centered Outcomes Research Institute, American Heart Association, American College of Cardiology:Active (exists now) ; Employee:Johns Hopkins School of Medicine :Active (exists now) ; Other (please indicate in the box next to the company name):National Institutes of Health Data Safety and Monitoring Board:Active (exists now) | Fatima Rodriguez: DO have relevant financial relationships ; Consultant:HealthPals:Past (completed) ; Consultant:Cleerly Health:Active (exists now) ; Consultant:Amgen:Active (exists now) ; Consultant:iRhythm:Active (exists now) ; Consultant:HeartFlow:Active (exists now) ; Consultant:Arrowhead Pharmaceuticals:Active (exists now) ; Consultant:Edwards:Active (exists now) ; Consultant:Inclusive Health:Active (exists now) ; Consultant:Esperion Therapeutics:Past (completed) ; Consultant:Kento Health:Active (exists now) ; Consultant:Movano Health:Active (exists now) ; Consultant:NovoNordisk:Past (completed) ; Consultant:Novartis:Active (exists now)
Meeting Info:

Scientific Sessions 2025

2025

New Orleans, Louisiana

Session Info:
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