Key result
Higher baseline NPAR linked to ~18% higher all-cause mortality in stroke survivors with elevated TyG.
Why the study?
The association between neutrophil percentage-to-albumin ratio (NPAR) and all-cause mortality in stroke survivors, and its variation across triglyceride-glucose index (TyG) strata, was unclear.
Is higher baseline neutrophil percentage-to-albumin ratio associated with increased all-cause mortality in stroke survivors stratified by triglyceride-glucose index?
Cohort (n=1,187)
Yes
Is higher baseline neutrophil percentage-to-albumin ratio associated with increased all-cause mortality in stroke survivors stratified by triglyceride-glucose index?
Hazard Ratio: 1.18
p-value: p=<.001
Higher neutrophil percentage-to-albumin ratio is independently associated with increased long-term all-cause mortality in stroke survivors, specifically those with intermediate to high insulin resistance as measured by the triglyceride-glucose index.
The neutrophil percentage-to-albumin ratio (NPAR) is a novel inflammatory biomarker with prognostic value in critical illnesses, but its association with outcomes in stroke survivors remains unclear. No prior study has explored whether this association differs across triglyceride-glucose index (TyG) strata, a surrogate marker of insulin resistance (IR) and metabolic disturbance in cardiovascular disease. Data from the National Health and Nutrition Examination Survey 1999 to 2018 were analyzed for 1187 stroke survivors aged 40 to 80 years. Kaplan-Meier curves, multivariate Cox models, restricted cubic spline (RCS) analysis, and subgroup analyses were used to examine the relationship between baseline NPAR and all-cause mortality across TyG levels. Over a median follow-up of 86 months, 496 (41.79%) of the 1187 participants died; median survival was 133 months. Kaplan-Meier analysis showed significant mortality differences across NPAR tertiles in all participants and within intermediate- and high-IR groups (all P < .001). As a continuous variable, NPAR was significantly associated with mortality in the intermediate-risk (hazard ratio = 1.18) and high-risk (hazard ratio = 1.10) groups, but not in the low-risk group. As a categorical variable, the highest NPAR tertile (T3) was associated with higher mortality across all adjustment models in IR intermediate- and high-risk groups, whereas in the IR low-risk group, significance was observed only in the minimally adjusted model. Restricted cubic spline analysis revealed a linear association between NPAR and mortality in all participants (P for nonlinear = .291), as well as in IR intermediate- and high-risk groups, but no association in the IR low-risk group (P for overall = .187). Subgroup analyses showed significant interactions across TyG subgroups (P for interaction = .047). Two sensitivity analyses confirmed the stability of the main findings. Monitoring NPAR levels alongside TyG-based stratification may facilitate comprehensive risk assessment and inform targeted management strategies for stroke survivors.
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Liu et al. (2026) conducted a cohort in Stroke (n=1,187). Neutrophil percentage-to-albumin ratio (NPAR) vs. Lower NPAR levels was evaluated on All-cause mortality (HR 1.18, p=<.001). Higher baseline neutrophil percentage-to-albumin ratio was associated with increased all-cause mortality in stroke survivors with intermediate (HR 1.18) and high (HR 1.10) triglyceride-glucose levels.
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