Key result
Higher CT-derived EATVI linked to ~45% higher post-PCI MACE risk per SD in AMI.
Why the study?
MACE remain common after successful PCI in patients with AMI. Although EATVI from routine non-contrast chest CT may reflect residual cardiometabolic and inflammatory risk, its association with post-PCI MACE and incremental prognostic value beyond conventional clinical risk markers remain incompletely understood.
Does non-contrast chest CT-derived epicardial adipose tissue volume index (EATVI) predict major adverse cardiovascular events and improve risk stratification beyond conventional clinical markers in patients with acute myocardial infarction undergoing PCI?
Cohort (n=367)
Blinded outcome adjudication
No
Does non-contrast chest CT-derived epicardial adipose tissue volume index (EATVI) predict major adverse cardiovascular events and improve risk stratification beyond conventional clinical markers in patients with acute myocardial infarction undergoing PCI?
Answers are grounded in this paper and cite their sources.
Routine non-contrast chest CT-derived epicardial adipose tissue volume index (EATVI) is independently associated with post-PCI MACE in acute myocardial infarction patients and provides modest incremental prognostic value beyond the GRACE score and conventional clinical risk factors.
Background Major adverse cardiovascular events (MACE) remain common after successful percutaneous coronary intervention (PCI) in patients with acute myocardial infarction (AMI). Epicardial adipose tissue volume index (EATVI) derived from routine non-contrast chest computed tomography (CT) may reflect residual cardiometabolic and inflammatory risk, but its association with post-PCI MACE and its incremental prognostic value beyond conventional clinical risk markers remain incompletely understood. Methods The final cohort comprised 367 patients with AMI who underwent PCI and non-contrast chest CT between January 2023 and December 2024. EATVI was calculated by indexing semi-automatically segmented EAT volume to body surface area. The endpoint was first major adverse cardiovascular event (MACE), comprising cardiac death, recurrent myocardial infarction, or rehospitalization for heart failure or unstable or progressive angina. Kaplan–Meier analysis, restricted cubic splines, and sequential Cox models assessed associations. Machine-learning-assisted screening informed a four-variable model that was internally validated using 1,000 bootstrap resamples and converted into an integer score. We compared the model with the Global Registry of Acute Coronary Events (GRACE) score alone and GRACE plus EATVI. Results During a median 26.38-month follow-up, 91 patients (24.8%) experienced MACE. Event rates increased from 16.3% to 31.1% across EATVI tertiles (log-rank P = 0.018). Each 22.9 mL/m² increase in EATVI was independently associated with MACE in the fully adjusted model (hazard ratio 1.47, 95% confidence interval 1.18–1.84; P < 0.001). Adding EATVI increased the GRACE C-index from 0.527 to 0.601 ( P = 0.033). The simplified model achieved a C-index of 0.682 (bootstrap-corrected: 0.671) and bootstrap-corrected 6-, 12-, and 24-month areas under the curve of 0.725, 0.709, and 0.690. The integer score separated low-, intermediate-, and high-risk groups, with MACE rates of 11.3%, 24.5%, and 48.1%, respectively (log-rank P < 0.001). Conclusions Routine non-contrast chest CT-derived EATVI identified residual risk after PCI for AMI and improved prognostic assessment beyond GRACE. The simplified model showed moderate internally validated discrimination, but external validation is required before clinical use.
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Zhang et al. (2026) conducted a cohort in Acute myocardial infarction undergoing percutaneous coronary intervention (n=367). Epicardial adipose tissue volume index (EATVI, per 1-SD [22.91 mL/m²] increase) vs. Lower EATVI / T1 reference (≤65.27 mL/m²) was evaluated on First post-discharge major adverse cardiovascular event (MACE: cardiovascular death, recurrent myocardial infarction, heart-failure hospitalization, ischemia-driven unplanned coronary revascularization, or hospitalization for unstable angina) (HR 1.45, 95% CI 1.17-1.79, p=<0.001). Each 1-SD (22.9 mL/m²) increase in non-contrast chest CT-derived EATVI was independently associated with higher post-PCI MACE risk in AMI patients (HR 1.45, 95% CI 1.17-1.79; P<0.001).
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