Is acute cholecystitis associated with an increased Electrical Risk Score and altered electrocardiographic markers of ventricular repolarization heterogeneity compared to healthy controls?
253 adults (153 with acute cholecystitis and 100 age- and sex-matched healthy controls), mean age 50.9 in the patient group, 58.2% female. Excluded: <18 years, pregnant, history of cardiac surgery, diagnosed malignancy, chronic heart disease, electrolyte imbalance, bundle branch block or arrhythmia on ECG, or receiving antiarrhythmic therapy.
Acute cholecystitis (observational exposure)
Age- and sex-matched healthy controls without acute inflammatory disease or known structural heart disease, with normal baseline ECG
Electrical Risk Score (ERS) derived from 12-lead ECG (sum of 6 binary parameters: heart rate, QTc interval, Tp-e interval, LVH, QRS transition zone, and frontal QRS-T angle)surrogate
Acute cholecystitis is associated with elevated electrocardiographic markers of ventricular repolarization heterogeneity, suggesting a cross-sectional electrophysiological impact of acute systemic inflammation.
This study investigated the association between the Electrical Risk Score (ERS), derived from 12-lead electrocardiography (ECG), and electrocardiographic markers related to ventricular arrhythmia risk in patients with acute cholecystitis (AC), using conventional statistical analyses and machine learning–based exploratory analyses. Given the cross-sectional study design, clinical cardiovascular outcomes and longitudinal prognostic effects were not assessed. In this prospective cross-sectional study, 153 patients diagnosed with AC and 100 age- and sex-matched healthy controls were enrolled. The ERS was calculated as the sum of six binary ECG parameters (range 0–6), and its individual components were compared between groups. The Tp–e interval (reflecting transmural dispersion of ventricular repolarization) and the frontal QRS–T angle (representing spatial heterogeneity between depolarization and repolarization vectors) were also analyzed. Six ensemble ML models including CatBoost and XGBoost were trained to estimate ERS variability using demographic, laboratory, and ECG variables. Model interpretation was performed using SHAP (Shapley Additive Explanations) analysis to improve transparency of model behavior. ERS was significantly higher in the AC group (2.1 ± 1.0) compared with controls (1.36 ± 0.71; p < 0.001). QT and QTc intervals, frontal QRS–T angle, and delayed QRS transition zone were significantly increased in AC patients. Laboratory markers including glucose, AST, ALT, hs-CRP, and WBC counts were also elevated in the AC group. Multivariate regression analysis identified AC, age, and AST as independent factors associated with ERS. Among ML models, CatBoost demonstrated the highest internal predictive performance for ERS estimation (R² = 0.9929, RMSE = 0.0578). Because ERS is derived from electrocardiographic parameters that were also included among model inputs, these predictive metrics should be interpreted cautiously. SHAP analysis indicated that heart rate, Tp–e interval, QTc interval, and frontal QRS–T angle were the most influential contributors to ERS estimation. Sensitivity analyses excluding ERS component variables suggested that systemic factors such as electrolyte balance and inflammatory markers may contribute to ERS variability, although their influence was weaker than that of electrophysiological parameters. Clinical endpoints such as arrhythmia, sudden cardiac death, or mortality were not evaluated. ERS values were significantly elevated in patients with AC and were associated with ECG markers reflecting ventricular repolarization heterogeneity. These findings indicate a cross-sectional electrophysiological association rather than evidence of prognostic utility. The integration of explainable ML techniques provided an interpretable exploratory framework for examining ERS variability, although no inference regarding prediction of future cardiovascular events can be drawn from the present data. Prospective longitudinal studies are required to determine whether ERS has independent clinical or prognostic relevance in this population.
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Yönder et al. (Sat,) studied this question.
www.synapsesocial.com/papers/69eefd9bfede9185760d4583 — DOI: https://doi.org/10.1186/s12872-026-05893-8
Hüseyin Yönder
Mustafa Beğenç Taşcanov
Gencay Sarıışık
BMC Cardiovascular Disorders
Harran University
Kahramanmaraş Sütçü İmam University
Samsun University
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