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American Heart Association

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Final ID: MP2292

Evaluation of the PREVENT Risk Assessment Tool and Visceral Adiposity: Insights from the UK Biobank

Abstract Body (Do not enter title and authors here): Background: Visceral adipose tissue (VAT) is a metabolically active fat depot strongly associated with cardiometabolic disease. This study evaluates whether MRI-derived VAT enhances the discrimination and calibration of the PREVENT model for atherosclerotic cardiovascular disease (ASCVD) heart failure (HF), and total cardiovascular disease (CVD) in a large, population-based cohort.
Methods: We included 38,373 UK Biobank participants who underwent abdominal MRI and had no known CVD at baseline. We assessed whether adding VAT to PREVENT would improve model performance using C-statistics and net reclassification improvement (NRI).
Results: The mean age was 54.86 years (SD 7.49), and 52% of participants were female. The median VAT volume was 3.58L (IQR:2.14-5.33). Using the overall median VAT value as the threshold, higher visceral adiposity (>3.58L) was associated with significantly increased risk of ASCVD (HR: 1.32, 95% CI: 1.15–1.51), heart failure (HR: 1.55, 95% CI: 1.27–1.89), and total CVD (HR: 1.38, 95% CI: 1.23–1.55) adjusting for age and sex (Figure 1). Adding VAT to the PREVENT model did not significantly improve discrimination for ASCVD (C-statistic 0.731 vs. 0.729, p = 0.85), nor for HF or total CVD. However, VAT significantly improved reclassification: NRI for ASCVD was 0.37 (95% CI: 0.30–0.33), for HF was 0.48 (95% CI: 0.35–0.61), and for total CVD was 0.37 (95% CI: 0.28–0.46) (Table 1). The association between VAT and all outcomes remained robust after adjustment for age and sex.
Conclusions: MRI-measured visceral adiposity is associated with increased risk of ASCVD, HF, and total CVD. While VAT did not improve overall discrimination of the PREVENT model, it significantly enhanced reclassification—particularly for HF. This suggests that VAT may improve individualized cardiovascular risk stratification and inform targeted preventive strategies.
  • Alebna, Pamela  ( Virginia Commonwealth University , Chester , Virginia , United States )
  • Salloum, Fadi  ( VIRGINIA COMMONWEALTH UNIV , Richmond , Virginia , United States )
  • Shapiro, Michael  ( Wake Forest Univ School of Medicine , Winston Salem , North Carolina , United States )
  • Mehta, Anurag  ( Virginia Commonwealth University , Chester , Virginia , United States )
  • Ambrosio, Matthew  ( Virginia Commonwealth University , Chester , Virginia , United States )
  • Dod, Rohan  ( Virginia Commonwealth University , Chester , Virginia , United States )
  • Campbell, Matthew  ( VCU Health , Richmond , Virginia , United States )
  • Carbone, Salvatore  ( Eastern Virginia Medical School , Norfolk , Virginia , United States )
  • Chew, Nicholas  ( Department of Cardiology, National University Heart Centre, National University Health System, Singapore , Singapore , Singapore )
  • Pagidipati, Neha  ( DCRI , Durham , North Carolina , United States )
  • Quyyumi, Arshed  ( EMORY UNIVERSITY , Atlanta , Georgia , United States )
  • Sperling, Laurence  ( EMORY UNIV , Atlanta , Georgia , United States )
  • Author Disclosures:
    Pamela Alebna: DO NOT have relevant financial relationships | Fadi Salloum: DO have relevant financial relationships ; Research Funding (PI or named investigator):NIH:Active (exists now) ; Advisor:NovoMedix, Inc:Active (exists now) ; Research Funding (PI or named investigator):AHA:Active (exists now) | Michael Shapiro: DO have relevant financial relationships ; Consultant:Ionis:Past (completed) ; Consultant:Arrowhead:Past (completed) ; Consultant:Regeneron:Past (completed) ; Researcher:New Amsterdam:Active (exists now) ; Researcher:Merck:Active (exists now) ; Researcher:Novartis:Active (exists now) ; Researcher:Esperion:Active (exists now) ; Researcher:Cleerly:Active (exists now) ; Researcher:Amgen:Active (exists now) ; Consultant:Novo Nordisk:Active (exists now) ; Consultant:Tourmaline:Active (exists now) ; Consultant:Merck:Active (exists now) ; Consultant:New Amsterdam:Past (completed) ; Consultant:Novartis:Active (exists now) | Anurag Mehta: DO have relevant financial relationships ; Research Funding (PI or named investigator):Amgen:Active (exists now) ; Research Funding (PI or named investigator):Novartis:Active (exists now) | Matthew Ambrosio: DO NOT have relevant financial relationships | Rohan Dod: DO NOT have relevant financial relationships | Matthew Campbell: DO NOT have relevant financial relationships | Salvatore Carbone: No Answer | Nicholas Chew: No Answer | Neha Pagidipati: DO have relevant financial relationships ; Research Funding (PI or named investigator):Alnylam:Active (exists now) ; Consultant:Esperion:Active (exists now) ; Consultant:Eli Lilly:Active (exists now) ; Consultant:Corsera:Active (exists now) ; Consultant:Corcept:Active (exists now) ; Consultant:Boehringer Ingelheim:Active (exists now) ; Consultant:Bayer:Active (exists now) ; Consultant:Amgen:Active (exists now) ; Research Funding (PI or named investigator):Merck:Active (exists now) ; Research Funding (PI or named investigator):Novo Nordisk:Active (exists now) ; Research Funding (PI or named investigator):Novartis:Active (exists now) ; Research Funding (PI or named investigator):Eli Lilly:Active (exists now) ; Research Funding (PI or named investigator):Boehringer Ingelheim:Active (exists now) ; Research Funding (PI or named investigator):Bayer:Active (exists now) ; Research Funding (PI or named investigator):Amgen:Active (exists now) | Arshed Quyyumi: DO NOT have relevant financial relationships | Laurence Sperling: DO NOT have relevant financial relationships
Meeting Info:

Scientific Sessions 2025

2025

New Orleans, Louisiana

Session Info:

Charting the Future: Cardiovascular Disease Risk Prediction

Monday, 11/10/2025 , 10:45AM - 12:00PM

Moderated Digital Poster Session

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