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. 2025 Jul 26:18:9935-9949.
doi: 10.2147/JIR.S532319. eCollection 2025.

Association of Neutrophil Percentage-to-Albumin Ratio with All-Cause and Cardiovascular Mortality in Maintenance Hemodialysis Patients: A Retrospective Study

Affiliations

Association of Neutrophil Percentage-to-Albumin Ratio with All-Cause and Cardiovascular Mortality in Maintenance Hemodialysis Patients: A Retrospective Study

Hongying Jiang et al. J Inflamm Res. .

Abstract

Aim: Patients undergoing maintenance hemodialysis (MHD) are prone to chronic inflammation, which often leads to the elevation of various inflammatory biomarkers. This study aims to investigate whether the neutrophil percentage-to-albumin ratio (NPAR), a novel biomarker linked to inflammation, increases the likelihood of both overall and cardiovascular mortality in these patients.

Methods: This retrospective cohort study, conducted across multiple centers, utilized data from the China Renal Data System (CRDS) Database collected between 2010 and 2022. A total of 10,067 eligible participants were included, with follow-up data available until December 31, 2022. Univariate and multivariate Cox regression analyses, Kaplan-Meier survival curves, competing risk plots, and restricted cubic splines were applied to investigate the association between NPAR and both overall and cardiovascular mortality in patients undergoing MHD. Additionally, time-dependent ROC analysis and C-index were employed to assess the predictive ability of NPAR for short-term and long-term outcomes in MHD patients.

Results: Among 10,067 eligible individuals, 1759 deaths from any cause were recorded over a median follow-up period of 50.9 months, with 453 of these deaths attributed to cardiovascular causes. Multivariate Cox regression models revealed that high NPAR levels were significantly associated with both all-cause mortality (HR 3.73, 95% CI 2.94-4.73) and cardiovascular mortality (HR 2.38, 95% CI 1.50-3.79). In subgroup analysis, the effect of elevated NPAR levels on the prediction of all-cause mortality was consistent across the seven pre-specified subgroup strata (all P for interaction > 0.05). Sensitivity analysis confirmed that NPAR remained significantly associated with all-cause mortality. Time-dependent ROC analysis showed that the AUC for NPAR in predicting all-cause mortality at overall, 1, 3, 5, and 10 years was 0.69, 0.70, 0.68, 0.65, and 0.62, respectively. For cardiovascular mortality, the corresponding values were 0.65, 0.68, 0.65, 0.64, and 0.61, respectively. For all-cause mortality, the adjusted C-index was 0.76 (95% CI: 0.74-0.78), while for cardiovascular mortality, the adjusted C-index was 0.82 (95% CI: 0.79-0.85).

Conclusion: In MHD patients, elevated NPAR levels were significantly associated with an increased risk of both overall and cardiovascular mortality, and demonstrated greater accuracy in predicting short-term outcomes.

Keywords: China renal data system database; all-cause mortality; cardiovascular mortality; hemodialysis; neutrophil percentage-to-albumin ratio.

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Conflict of interest statement

The authors report no conflicts of interest in this work.

Figures

Figure 1
Figure 1
Flowchart of sample selection from the CRDS.
Figure 2
Figure 2
Kaplan-Meier analysis of all-cause mortality in NPAR quartile subgroups (P for Log-rank< 0.0001).
Figure 3
Figure 3
Competing risk analysis of cumulative incidence of cardiovascular disease mortality (Gray = 87.78, p<0.001).
Figure 4
Figure 4
Restricted cubic spline for NPAR and all-cause and cardiovascular mortality. (A) all-cause mortality, P for nonlinear<0.001, P for overall < 0.001, knot = 18.88). (B) cardiovascular mortality, P for nonlinear<0.014, P for overall <0.001, knot = 18.88.
Figure 5
Figure 5
Subgroup analysis of the relationship between NPAR and all-cause mortality.
Figure 6
Figure 6
Time-dependent ROC curve for all-cause mortality and cardiovascular mortality in MHD. (A) all-cause mortality). (B) cardiovascular mortality.
Figure 7
Figure 7
Time-dependent AUC curves for all-cause and cardiovascular mortality in MHD. (A) all-cause mortality). (B) cardiovascular mortality.

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