Key result
Hepatic steatosis on coronary CTA is linked to ~300% higher MACE risk in suspected stable CAD.
Why the study?
The study aimed to evaluate whether concurrent assessment of hepatic steatosis during coronary CTA provides additional risk stratification in patients with suspected stable CAD.
Does concurrent assessment of hepatic steatosis during coronary CTA improve risk stratification for MACE in outpatients with suspected stable CAD?
Population
1148 Japanese outpatients without CAD history undergoing coronary CTA for suspected stable CAD
Comparison
Presence vs absence of hepatic steatosis
Design
Prospective study
Follow-up
Median 3.9 years
Authors
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Concurrent evaluation of hepatic steatosis during coronary CTA provides incremental prognostic value for MACE over standard CTA findings and clinical risk scores in patients with suspected stable CAD.
Cohort (n=1,148)
Outcome assessors blinded
No
Does concurrent assessment of hepatic steatosis during coronary CTA improve risk stratification for MACE in outpatients with suspected stable CAD?
Hazard Ratio: 4.01 (95% CI 2.12–7.59)
Absolute Event Rate: 9.3% vs 1.9%
p-value: p=<0.001
Concurrent evaluation of hepatic steatosis during coronary CTA provides incremental prognostic value for MACE over standard CTA findings and clinical risk scores in patients with suspected stable CAD.
Ichikawa et al. (2021) conducted a cohort in Suspected stable coronary artery disease (n=1,148). Hepatic steatosis vs. Absence of hepatic steatosis was evaluated on Major adverse cardiac events (MACE), a composite of cardiac death, acute coronary syndrome, and late revascularization (HR 4.01, 95% CI 2.12-7.59, p=<0.001). Hepatic steatosis concurrently assessed during coronary CTA was independently associated with a significantly increased risk of major adverse cardiac events (HR 4.01) in patients with suspected stable CAD.
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