Key result
Pan-immune-inflammation value fails to independently predict mortality on multivariable analysis.
Why the study?
The study investigated the association between the pan-immune-inflammation value (PIV) and mortality in patients with heart failure with reduced ejection fraction (HFrEF).
Does the pan-immune-inflammation value (PIV) predict all-cause mortality in patients with heart failure with reduced ejection fraction (HFrEF)?
Cohort (n=419)
Yes
Does the pan-immune-inflammation value (PIV) predict all-cause mortality in patients with heart failure with reduced ejection fraction (HFrEF)?
In patients with chronic HFrEF, the pan-immune-inflammation value (PIV) is not an independent predictor of all-cause mortality when adjusted for established clinical and biochemical risk factors such as LVEF, NYHA class, NT-proBNP, BMI, sodium, and lymphocyte count.
PIV >696 should not guide mortality risk assessment in HFrEF; leaves open whether inflammation indices add value beyond established predictors.
Objective: We aimed to investigate the association between the pan-immune-inflammation value (PIV) and mortality in patients with heart failure with a reduced ejection fraction (HFrEF), along with clinical and biochemical parameters. Methods: In this retrospective cohort study, 419 patients diagnosed with HFrEF between January 2014 and December 2023 were analyzed. Data on demographic features, comorbidities, cardiac parameters [New York Heart Association (NYHA) classification, left ventricular ejection fraction (LVEF), ventricular dimensions], medication use, and laboratory findings (PIV, N-terminal pro-B-type natriuretic peptide [NT-proBNP], electrolytes, and complete blood count) were collected from institutional and national records. Results: Mortality occurred in 22.91% of patients. PIV > 696 was significantly associated with mortality (sensitivity: 37.5%, specificity: 78.64%, p = 0.006), but it was not an independent predictor in multivariate analysis. Instead, low body mass index (BMI), increased end-systolic diameter, reduced LVEF, advanced NYHA class (III/IV), elevated NT-proBNP, hyponatremia, and lymphopenia were identified as independent predictors (all p < 0.001). Conclusions: Although PIV was associated with mortality in patients with HFrEF, it did not independently predict outcomes beyond established risk factors. These results suggest that while inflammation may contribute to HFrEF pathophysiology, traditional clinical and biochemical markers remain more reliable for prognostication.
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Derviş et al. (2025) conducted a cohort in Heart failure with reduced ejection fraction (HFrEF) (n=419). Pan-immune-inflammation value (PIV) vs. Lower PIV (≤696) or survivor group was evaluated on All-cause mortality (AUC 0.592, 95% CI 0.527-0.658, p=0.006). Pan-immune-inflammation value >696 was associated with mortality in univariate ROC analysis (AUC 0.592, p=0.006), but failed to independently predict mortality in multivariable analysis (p=0.873).
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