Abstract 4335849: Improvements in Diagnostic and Therapeutic Cardiovascular Risk Assessment Through Total Plaque Volume Burden: An Analysis of the Fish&Chips Study

S Shyon Parsa (Stanford University Hospital, Mountain View, California, United States) A Allison Peng (Johns Hopkins School of Medicine, Baltimore, Maryland, United States) T Timothy Fairbairn (Liverpool Heart and Chest Hospital, Liverpool, United Kingdom) J Jack Bell (Liverpool Heart and Chest Hospital, Liverpool, United Kingdom) S Souma Sengupta (Heartflow Inc, Mountain View, California, United States) S Sarah Mullen (Heartflow, San Carlos, California, United States) C Campbell Rogers (Heartflow, San Carlos, California, United States) S Seth Martin (Johns Hopkins School of Medicine, Baltimore, Maryland, United States) F Fatima Rodriguez

Abstract

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.

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)

S

Shyon Parsa

Stanford University Hospital, Mountain View, California, United States

A

Allison Peng

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

T

Timothy Fairbairn

Liverpool Heart and Chest Hospital, Liverpool, United Kingdom

J

Jack Bell

Liverpool Heart and Chest Hospital, Liverpool, United Kingdom

S

Souma Sengupta

Heartflow Inc, Mountain View, California, United States

S

Sarah Mullen

Heartflow, San Carlos, California, United States

C

Campbell Rogers

Heartflow, San Carlos, California, United States

S

Seth Martin

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

F

Fatima Rodriguez