Key result
Higher neutrophil percentage-to-albumin ratio is linked to ~62% higher mortality in HFpEF.
Why the study?
Does an elevated neutrophil percentage-to-albumin ratio predict diuretic resistance and mortality in patients with heart failure with preserved ejection fraction?
Cohort (n=1,487)
No
Does an elevated neutrophil percentage-to-albumin ratio predict diuretic resistance and mortality in patients with heart failure with preserved ejection fraction?
NPAR is a simple, accessible biomarker that independently predicts diuretic resistance and mid-term mortality in patients with HFpEF, highlighting the role of systemic inflammation in disease progression.
BACKGROUND: Heart failure with preserved ejection fraction (HFpEF) is increasingly recognized as a systemic inflammatory and metabolic disorder. Diuretic resistance remains a major therapeutic challenge in this population. The neutrophil percentage-to-albumin ratio (NPAR), a novel marker of systemic inflammation, may serve as a predictor of diuretic resistance and adverse outcomes in HFpEF. METHODS: This retrospective cohort study included 1 487 HFpEF patients treated between January 2017 and August 2022. Patients were divided into 2 groups: those with and without diuretic resistance. Clinical, laboratory, and echocardiographic parameters were compared between groups. Receiver-operating characteristic (ROC) analysis, logistic regression, and Kaplan-Meier survival analyses were used to determine predictive and prognostic factors. RESULTS: Patients with diuretic resistance exhibited significantly higher NPAR values, H2FPEF scores, NT-proBNP levels, and echocardiographic indices of diastolic dysfunction. ROC analysis identified an NPAR cut-off of 13.98 for predicting diuretic resistance (AUC = 0.892, 95% CI: 0.741-0.993, P < .01). Multiple Cox's proportional hazard regression analysis revealed that NPAR, hs-C-reactive protein, sodium, NT-proBNP, left atrial volume index, and E/e' were independent predictors of diuretic resistance. Kaplan-Meier analysis demonstrated increased mid-term mortality in patients with NPAR > 13.98 (log-rank P < .001). Elevated NPAR independently predicted mortality in the diuretic-resistant HFpEF subgroup (OR = 1.95, 95% CI: 1.80-2.22, P < .001). CONCLUSION: NPAR is a simple and accessible inflammatory biomarker that independently predicts diuretic resistance and mortality in HFpEF. The findings underscore the role of systemic inflammation in HFpEF pathophysiology and highlight NPAR as a potential tool for early risk stratification and therapeutic decision-making.
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Vural et al. (2026) conducted a cohort in Heart failure with preserved ejection fraction (HFpEF) (n=1,487). Neutrophil percentage-to-albumin ratio (NPAR) vs. Lower NPAR was evaluated on Mid-term all-cause mortality (HR 1.62, 95% CI 1.31-1.94, p=<0.001). Elevated neutrophil percentage-to-albumin ratio independently predicted mid-term all-cause mortality (HR 1.62) and diuretic resistance in patients with heart failure with preserved ejection fraction.
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