Key result
Top cholesterol-HDL-glucose index quartile linked to ~176% higher 30-day mortality in AMI patients.
Why the study?
The prognostic relevance of the cholesterol-HDL-glucose index during acute myocardial infarction remains uncertain.
Does an elevated cholesterol-HDL-glucose (CHG) index predict increased 30-day and 365-day mortality in patients with acute myocardial infarction?
Cohort (n=5,187)
Yes
Does an elevated cholesterol-HDL-glucose (CHG) index predict increased 30-day and 365-day mortality in patients with acute myocardial infarction?
Hazard Ratio: 2.76 (95% CI 1.57–4.86)
p-value: p=<0.001
An elevated cholesterol-HDL-glucose (CHG) index is associated with increased 30-day and 365-day all-cause mortality in patients with acute myocardial infarction, providing complementary prognostic information to established risk scores like GRACE.
Elevated CHG index may aid AMI risk stratification; hypothesis-generating and requires prospective validation before practice change.
The cholesterol–HDL–glucose (CHG) index integrates total cholesterol, HDL-C, and glucose, but its prognostic relevance during acute myocardial infarction (AMI) remains uncertain. We evaluated its associations with 30-day and 365-day mortality and compared its prognostic performance with conventional metabolic markers and GRACE. This retrospective two-cohort study included 4,167 clinical-cohort patients with AMI and 1,020 patients in a supportive MIMIC-IV replication cohort. CHG was modeled continuously and by clinical-cohort quartiles. The clinical-cohort upper-quartile cutoff was applied unchanged in MIMIC-IV as a grouping rule; cohort-specific models were fitted. Analyses included multivariable Cox regression, restricted cubic splines, subgroup and sensitivity analyses, time-dependent ROC, and nested GRACE comparisons. In the clinical cohort, the fully adjusted hazard ratios (HRs) for the highest versus lowest CHG quartile were 2.76 (95% CI, 1.57–4.86) for 30-day mortality and 2.40 (95% CI, 1.50–3.86) for 365-day mortality (both P < 0.001). The corresponding HRs per 1-unit increase were 2.16 (95% CI, 1.54–3.02) and 1.88 (95% CI, 1.41–2.51), respectively (both P < 0.001). CHG remained associated with both outcomes after accounting for GRACE, and adding CHG improved model fit. In MIMIC-IV, applying the clinical-cohort cutoff classified 40.6% of patients as high CHG. For 30-day mortality, the fully adjusted Cox estimate was HR 1.41 (95% CI, 0.98–2.04; P = 0.066), and the fixed-horizon logistic sensitivity estimate was OR 1.60 (95% CI, 1.02–2.52; P = 0.041). No significant 365-day association was observed in MIMIC-IV. Elevated CHG was associated with 30-day and 365-day mortality in the clinical AMI cohort and retained prognostic information alongside GRACE. As a readily calculable composite of routine glucose and lipid measurements, CHG may provide complementary information for metabolic risk assessment after AMI.
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Zhao et al. (2026) conducted a cohort in Acute Myocardial Infarction (n=5,187). Cholesterol-HDL-Glucose (CHG) index vs. Lowest CHG quartile was evaluated on 30-day all-cause mortality (HR 2.76, 95% CI 1.57-4.86, p=<0.001). The highest quartile of the cholesterol-HDL-glucose index was associated with a significantly increased risk of 30-day mortality (HR 2.76) compared to the lowest quartile in patients with acute myocardial infarction.
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