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Updated: May 23, 2026

Inducing and Characterizing Vesicular Steatosis in Differentiated HepaRG Cells
Published on: July 18, 2019
Hepatic Steatosis Is Associated With Increased Cardiovascular Risk Through Adverse Coronary Plaque Composition
Jan M Brendel1, Thomas Mayrhofer2, Nóra M Kerkovits3
1Department of Radiology, Cardiovascular Imaging Research Center (CIRC), Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; Department of Radiology, University of Tuebingen, Tuebingen, Germany.
Insights
Hepatic steatosis (fatty liver disease) is linked to a higher risk of major adverse cardiovascular events (MACE). This risk is partly explained by increased noncalcified plaque burden in coronary arteries, suggesting vulnerable atherosclerosis.
Area of Science:
- Cardiology
- Radiology
- Hepatology
Background:
- Hepatic steatosis is independently linked to major adverse cardiovascular events (MACE).
- The precise relationship between hepatic steatosis, coronary plaque characteristics, and MACE remains incompletely understood.
- Understanding this link is crucial for cardiovascular risk stratification.
Purpose of the Study:
- To investigate the association between hepatic steatosis and coronary plaque composition.
- To determine if hepatic steatosis predicts MACE independently of traditional risk factors and plaque burden.
- To explore the mediating role of coronary plaque characteristics in the hepatic steatosis-MACE relationship.
Main Methods:
- Analysis of 3,637 patients from the PROMISE trial randomized to the CT arm.
- Hepatic steatosis assessed via non-contrast CT using hepatic and splenic attenuation.
- Coronary CT angiography quantified plaque volume and burden; multivariable regression and mediation analyses assessed outcomes.
Main Results:
- 25.5% of patients had hepatic steatosis, associated with higher MACE rates.
- Hepatic steatosis correlated with greater noncalcified plaque burden (NCPB) after risk factor adjustment.
- Hepatic steatosis independently predicted increased MACE risk, with NCPB mediating 11% of this association.
Conclusions:
- Hepatic steatosis is associated with increased noncalcified plaque burden and MACE risk.
- Noncalcified plaque burden partially mediates the relationship between hepatic steatosis and MACE.
- Findings suggest a link between hepatic steatosis and vulnerable coronary atherosclerosis, supporting integrated cardiometabolic risk assessment.
Background & Aims:
Hepatic steatosis has been associated with major adverse cardiovascular events independently of other cardiovascular risk factors and the severity of coronary artery disease. Nevertheless, the relationship between hepatic steatosis, coronary plaque composition, and major adverse cardiovascular events remains unclear.
Methods:
A central core laboratory analyzed Prospective Multicenter Imaging Study for Evaluation of Chest Pain (PROMISE) participants randomized to the computed tomography arm. Hepatic steatosis was assessed on noncontrast computed tomography using standard hepatic and splenic attenuation methods. Coronary computed tomography angiography was used to quantify total, calcified, noncalcified, and low-attenuation plaque volume and burden (% vessel volume). Multivariable regression and mediation analyses assessed relationships between hepatic steatosis, plaque components, and major adverse cardiovascular events (death, myocardial infarction, unstable angina hospitalization). The median follow-up was 25 months (interquartile range, 18-33 months).
Results:
Among 3637 patients (age, 60.6 ± 8.2 years; 51.4% female), 25.5% had hepatic steatosis and were slightly younger, more often male, had more cardiovascular risk factors, and had a higher rate of major adverse cardiovascular events (4.1% vs 2.5%) (all P < .05). After adjustment for clinical risk factors, hepatic steatosis was associated with greater noncalcified plaque burden (β, 0.15%; 95% confidence interval, 0.04-0.27; P = .008). Hepatic steatosis was associated with increased risk of major adverse cardiovascular events independent of atherosclerotic cardiovascular disease risk score, obesity, obstructive stenosis, and noncalcified plaque burden (adjusted hazard ratio, 1.69; 95% confidence interval, 1.12-2.54; P = .012), whereas noncalcified plaque burden mediated 11% of the association between hepatic steatosis and major adverse cardiovascular events.
Conclusions:
Hepatic steatosis was associated with greater noncalcified plaque burden and increased risk of major adverse cardiovascular events, with noncalcified plaque burden accounting for a portion of this association, suggesting a link between hepatic steatosis and vulnerable coronary atherosclerosis. These findings support integrated cardiometabolic risk assessment in patients undergoing coronary computed tomography angiography.
Clinicaltrials:
gov number, NCT01174550.
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