Key result
Elevated albumin-corrected anion gap linked to ~6.5-fold higher ICU mortality in diabetic AMI patients.
Why the study?
Does the albumin-corrected anion gap (ACAG) predict ICU and in-hospital all-cause mortality in elderly critically ill diabetic patients with acute myocardial infarction?
Cohort (n=834)
Yes
Does the albumin-corrected anion gap (ACAG) predict ICU and in-hospital all-cause mortality in elderly critically ill diabetic patients with acute myocardial infarction?
Elevated albumin-corrected anion gap (ACAG) is an independent linear predictor of ICU and in-hospital all-cause mortality in elderly diabetic patients with severe AMI, and a clinical nomogram incorporating ACAG provides strong predictive discrimination for mortality risk.
May support ACAG for mortality risk stratification in elderly diabetic AMI; leaves open prospective validation before clinical adoption.
Objective Metabolic acidosis is a frequent acid-base imbalance in critically ill patients and is often associated with poor prognosis. This study aimed to evaluate the prognostic value of the albumin-corrected anion gap (ACAG) in predicting poor prognosis among diabetic patients with severe acute myocardial infarction (AMI). Methods A retrospective analysis was conducted using clinical data from 834 patients with AMI and comorbid diabetes mellitus, sourced from the Medical Information Mart for Intensive Care-IV (MIMIC-IV) database in the United States. Patients were classified into survival and non-survival groups based on intensive care unit (ICU) outcomes and further stratified into quartiles according to ACAG levels. Kaplan–Meier survival analysis and log-rank tests were used to assess the association between ACAG and short-term (7-day) and long-term mortality. Cox proportional hazard models were applied to evaluate the independent prognostic value of ACAG. Restricted cubic spline (RCS) analysis was used to visualize the non-linear relationship between ACAG and all-cause mortality in ICU and in-hospital settings. A nomogram prediction model incorporating ACAG was also constructed and validated. Results Among the 834 enrolled patients (61.05% male), the in-hospital and ICU mortality rates were 22.10% and 15.16%, respectively. Patients with ACAG values > 18.75 had significantly higher mortality compared to those with values < 15.75. After adjustment for potential confounders, elevated ACAG remained independently associated with an increased risk of death. RCS analysis revealed a positive linear association between ACAG levels and in-hospital and ICU mortality. Based on these findings, a nomogram prediction model incorporating ACAG was developed to estimate mortality risk in diabetic patients with acute AMI. Conclusion ACAG was significantly associated with both in-hospital and ICU all-cause mortality in diabetic patients with severe AMI. These findings suggest that ACAG may be a valuable prognostic biomarker for identifying high-risk individuals in this critically ill population.
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Zhan et al. (2026) conducted a cohort in Severe acute myocardial infarction with comorbid diabetes mellitus (n=834). Elevated albumin-corrected anion gap (ACAG, Quartile 4: 22.75-55.75 mmol/L) vs. Lowest ACAG quartile (Quartile 1: 8.25-15.75 mmol/L) was evaluated on Intensive care unit (ICU) all-cause mortality (HR 6.50, 95% CI 3.25-13.00, p=<0.001). Elevated albumin-corrected anion gap (Q4 vs Q1) was independently associated with higher ICU all-cause mortality (34.40% vs 5.98%; adjusted HR 6.50, 95% CI 3.25-13.00, P<0.001) in elderly diabetic AMI patients.
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