Mode
Text Size
Log in / Sign up

Higher systemic immune-inflammation index associated with increased mortality in interstitial lung diseaseCould a simple blood test help predict survival in serious lung disease?

AI-generated summary of the cited source, checked by automated accuracy review. How we work

Key Takeaway
Consider SII as a potential prognostic marker in ILD, but recognize this is an observational association requiring validation.

A retrospective cohort study investigated the association between the systemic immune-inflammation index (SII) and all-cause mortality in 366 patients with interstitial lung disease (ILD). The median follow-up was 20.6 months. The primary outcome was all-cause mortality, which occurred in 91 patients (24.9%). The study did not report a specific comparator group.

The main results showed that median SII was higher in deceased patients (1471.14) compared to survivors (1017.21). The SII demonstrated a statistically significant discriminatory ability for mortality, with an area under the curve (AUC) of 0.658 (95% CI 0.594–0.723). Survival was significantly lower in the high SII group compared to the low SII group (log-rank p < 0.001). No effect sizes for mortality risk were reported.

Safety and tolerability data were not reported. The study has several key limitations: it is a retrospective observational study, which establishes association but not causation. The generalizability is unclear as the clinical setting was not reported. The funding sources and potential conflicts of interest were also not reported.

For clinical practice, this study identifies a potential prognostic biomarker in ILD. However, the SII's clinical utility for risk stratification or guiding therapy remains unproven. The findings should be interpreted as hypothesis-generating, requiring validation in prospective studies before any consideration for integration into clinical decision-making.

Living with interstitial lung disease (ILD) means facing a lot of uncertainty. It's a group of serious conditions that scar the lungs, and doctors are always looking for better ways to understand how the disease might progress for each person. A new study looked back at the medical records of 366 ILD patients to see if a simple number calculated from a routine blood test—called the systemic immune-inflammation index (SII)—was connected to survival.

The findings show a clear link. Over a median follow-up of about 20 months, nearly a quarter of the patients died. Those who died had a significantly higher median SII level compared to those who survived. The analysis found that a higher SII score was statistically associated with a greater risk of death from any cause. The SII's ability to distinguish between higher and lower risk was modest but significant.

It's crucial to understand what this study does and doesn't tell us. This was a retrospective look at past data, which means it can only show an association, not prove that a high SII causes worse outcomes. The study didn't report on safety or side effects, as the SII is just a calculation from existing tests, not a treatment. The results are a promising signal that inflammation, as measured by this index, plays a role in ILD, but much more research is needed to see if this marker could ever be useful for guiding care in a doctor's office.

What this means for you:
A blood marker linked to inflammation is associated with higher mortality in interstitial lung disease.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
ObjectiveTo investigate the association between the systemic immune-inflammation index (SII) and all-cause mortality in patients with interstitial lung disease (ILD).MethodsThis retrospective cohort study included 366 patients with ILD. SII was calculated using peripheral blood counts and analyzed as both a continuous and categorical variable based on the optimal cutoff value determined by receiver operating characteristic (ROC) analysis. Kaplan–Meier survival curves were used to compare survival between SII groups. Univariable and multivariable Cox proportional hazards models were applied to evaluate the association between SII and all-cause mortality. Restricted cubic spline (RCS) analysis was performed to assess the dose–response relationship. Subgroup analyses were conducted to examine the robustness of the association.ResultsOver a median follow-up of 20.6 months, the primary outcome of all-cause mortality occurred in 91 patients (24.9%). The median SII was significantly higher in deceased patients compared with survivors (1471.14 vs. 1017.21). ROC analysis showed a statistically significant discriminatory ability of SII for mortality prediction (AUC = 0.658, 95% CI 0.594–0.723). Kaplan–Meier analysis demonstrated significantly lower survival in patients with high SII (log-rank p 
Free Newsletter

Clinical research that matters. Delivered to your inbox.

Join thousands of clinicians and researchers. No spam, unsubscribe anytime.