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Published on: August 28, 2018
Coronary Artery Disease and Major Adverse Cardiovascular Events in People With Hepatic Steatosis at Low
Julia Karady1,2, Thomas Mayrhofer1,3, Borek Foldyna1
1Cardiovascular Imaging Research Center, Harvard Medical School-Massachusetts General Hospital, Boston, Massachusetts, USA.
Insights
Hepatic steatosis (HS) increases cardiovascular event risk, even in individuals with low atherosclerotic cardiovascular disease (ASCVD) risk. This finding highlights HS as a significant, independent predictor of major adverse cardiovascular events (MACE).
Area of Science:
- Cardiology
- Hepatology
- Preventive Medicine
Background:
- Hepatic steatosis (HS) and a 10-year atherosclerotic cardiovascular disease (ASCVD) risk of ≥7.5% are independently associated with an elevated risk of cardiovascular events.
- Understanding the interplay between HS, ASCVD risk, and cardiovascular outcomes is crucial for risk stratification and preventive strategies.
Purpose of the Study:
- To evaluate the prevalence of underlying coronary artery disease (CAD) and the incidence of major adverse cardiovascular events (MACE) in patients with and without HS across different ASCVD risk strata.
- To determine if HS is an independent predictor of MACE in patients with low ASCVD risk.
Main Methods:
- Analysis of stable chest pain patients from the PROMISE trial who underwent coronary computed tomography (CT).
- HS and CAD were assessed using coronary CT. MACE included unstable angina, non-fatal myocardial infarction, and all-cause death.
- Multivariable Cox regression was employed to assess the association between HS and MACE, adjusting for CAD characteristics, particularly in patients with ASCVD risk <7.5%.
Main Results:
- Of 3702 patients, 1204 (32.5%) had ASCVD risk <7.5%, with 20.3% (244/1204) of these having HS.
- Patients with HS were younger, more frequently male, and had more risk factors compared to those without HS.
- Despite similar CAD characteristics, patients with HS exhibited significantly higher MACE rates compared to non-HS patients, both in the low (<7.5%) and high (≥7.5%) ASCVD risk groups. Notably, in the low ASCVD risk group, HS independently predicted MACE (aHR: 2.34, 95% CI: 1.01-5.43).
Conclusions:
- Individuals with hepatic steatosis and low ASCVD risk (<7.5%) have similar coronary artery disease characteristics as those without HS but experience a comparable rate of major adverse cardiovascular events as individuals with high ASCVD risk (≥7.5%).
- Hepatic steatosis is an independent predictor of MACE in patients with low ASCVD risk, suggesting it should be considered in cardiovascular risk assessment.
Background:
Hepatic steatosis (HS) and 10-year atherosclerotic cardiovascular disease (ASCVD) risk ≥ 7.5% are associated with increased risk for cardiovascular events.
Aim:
To assess underlying coronary artery disease (CAD) and major adverse cardiovascular event (MACE) among those with and without HS at different ASCVD risk.
Methods:
We evaluated stable chest pain patients receiving coronary computed tomography (CT) in the PROMISE trial. HS and CAD endpoints were defined on coronary CT. MACE was defined as unstable angina, non-fatal myocardial infarction, and all-cause death. Multivariable Cox regression, adjusting for CAD characteristics, assessed the association of HS with MACE for ASCVD < 7.5%.
Results:
One thousand two hundred and four of 3702 (32.5%) patients were at ASCVD < 7.5% and 20.3% (244/1204) of them had HS. Individuals with HS were younger (54.3 ± 5.2 vs. 55.8 ± 5.2; p < 0.001), more often males (40.2% [98/244] vs. 27.1% [260/960]; p < 0.001), had more risk factors/person (2.06 ± 0.89 vs. 1.93 ± 0.91; p = 0.047). CAD characteristics were similar between HS vs. non-HS patients at ASCVD < 7.5% and ASCVD ≥ 7.5% (all p > 0.05). Patients with HS had greater MACE rate compared to non-HS patients (ASCVD < 7.5%: 3.75%[9/244] vs. 1.5% [14/960]; p = 0.027 and ASCVD ≥ 7.5%: 4.7% [33/696] vs. 3.1% [56/1802]; p = 0.043). In patients without HS, MACE rate was higher in the ASCVD ≥ 7.5% vs. < 7.5% (3.1% [56/1802] vs. 1.5% [14/960]; p = 0.011). In patients with HS, MACE rates were not significantly different between ASCVD ≥ 7.5% vs. < 7.5% (4.7% [33/696] vs. 3.7% [9/244]; p = 0.484). In ASCVD < 7.5%, HS predicted MACE (aHR:2.34, 95%CI:1.01-5.43; p = 0.048), independent of CAD characteristics.
Conclusions:
Individuals with HS at ASCVD < 7.5% risk had similar CAD characteristics as patients without HS at < 7.5% ASCVD risk, yet experienced comparable MACE rates as those at ASCVD ≥ 7.5%.
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