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Published on: June 10, 2025
Lactate dehydrogenase-to-albumin ratio and adverse outcomes in patients with HFrEF and HFmrEF
Yaping Zhang1,2,3, Qianyu Ma1,2,3, Nana Hu1,2,3
1First Clinical Medical College, Lanzhou University, Lanzhou, Gansu Province, China.
Objective:
This study investigated the association between lactate dehydrogenase-to-albumin ratio (LAR) and adverse outcomes in patients with heart failure with reduced ejection fraction (HFrEF) and heart failure with mildly reduced ejection fraction (HFmrEF).
Methods:
This retrospective cohort study included 1,084 hospitalised patients with HFrEF or HFmrEF. It was approved by the Ethics Committee. Associations between LAR and endpoint events(HF-related readmissions, all-cause deaths, composite endpoints) were assessed using Cox regression, Kaplan-Meier curves, and restricted cubic spline analysis. The Fine-Grey model was applied for HF-related readmission to account for competing mortality. Subgroup and sensitivity analyses were performed to evaluate the robustness of the findings. Incremental predictive value of LAR was assessed using C-index, NRI, and IDI.
Results:
During a mean follow-up of 29.3 months, higher LAR was independently associated with increased risks of HF-related readmissions(HR:1.602, 95% CI:1.088-2.359), all-cause mortality (HR:2.008, 95% CI:1.155-3.492), and the composite endpoint (HR:1.648, 95% CI:1.184-2.295) (all P < 0.05). Kaplan-Meier analysis confirmed the highest cumulative event incidence in the highest LAR tertile (Log-rank P < 0.001). Restricted cubic spline analysis revealed a nonlinear relationship between LAR and all-cause mortality, with risk significantly increasing at LAR ≥ 4.82 (P-nonlinear < 0.001). The robustness of these findings was supported by multivariate subgroup and sensitivity analyses.
Conclusion:
Baseline LAR level is an independent predictor of HF readmission, all-cause mortality, and the combined endpoint in both HFrEF and HFmrEF patients, demonstrating clinical value for risk stratification.
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