# Admission systemic immune-inflammatory index predicts long-term mortality in patients with acute ischemic stroke: a retrospective analysis of the MIMIC-III database

**Authors:** Xiao Su, Xiuqing Tong, Ning Li, Boran Wang, Wei Gao, Yanmo Wang

PMC · DOI: 10.1186/s40635-026-00878-5 · Intensive Care Medicine Experimental · 2026-03-09

## TL;DR

A new inflammation-based index predicts long-term survival in stroke patients using hospital data.

## Contribution

This is the first study to show that the Aggregate Index of Systemic Inflammation (AISI) predicts stroke patient mortality over two years.

## Key findings

- High AISI levels correlate with 31% higher 90-day mortality in stroke patients.
- AISI above 5841.5 shows a gradual increase in mortality risk over two years.
- AISI is a promising predictor of long-term stroke outcomes.

## Abstract

The Aggregate Index of Systemic Inflammation (AISI) is a novel index based on platelets, neutrophils, and lymphocytes associated with the prognosis of patients with cancer and infectious diseases. However, its application in acute ischemic stroke (AIS) has rarely been reported. This study evaluated stroke prognosis using AISI by examining the relationship between levels of systemic immunoinflammatory indices at admission and patient outcomes at different times after onset.

This was a retrospective cohort study. The data from 1222 stroke patients were obtained from multiparameter intelligent monitoring in the Intensive Care III database (MIMIC-III). Cox proportional risk model was conducted to estimate the relation between AISI, all-cause mortality, and ischemic. The findings were further validated with restricted cubic spline (RCS) and subgroup analyses.

A total of 1222 patients with AIS were classified into tertiles based on AISI levels, tertile 1: low AISI, AISI levels less than 3881 (n = 408), tertile 2: medium AISI, AISI levels 3881 to 8354 (n = 408), and tertile 3: high AISI, AISI levels greater than 8354 (n = 407). After adjusting for multiple covariates, it was found that AISI was related to all-cause mortality in stroke patients. Patients with high AISI had a 31% increased risk of death after 90 days (HR = 1.31, 95% CI 1.03–1.67, P = 0.03) compared to patients with low AISI. Patients with high AISI had a 27% increased risk of death after 365 days (HR = 1.27, 95% CI 1.03–1.58, P = 0.029) than low AISI patients. Furthermore, compared with patients with low AISI, patients with high AISI had a 30% increased risk of death after two years (HR = 1.30, 95% CI 1.05–1.60, P = 0.014). During the 2-year follow-up period, the use of RCS showed that the mortality rate gradually increased with the increase of AISI value after 5841.5.

Systemic immunoinflammatory indices are related to long-term adverse outcomes in patients with AIS. Therefore, AISI is a promising inflammatory index for predicting the long-term prognosis of stroke.

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}
- **Diseases:** dyslipidemia (MESH:D050171), death (MESH:D003643), brain injury (MESH:D001930), hypertension (MESH:D006973), artery atherosclerosis (MESH:D050197), coronary atherosclerotic heart disease (MESH:D003327), brain damage (MESH:D001925), viral infections (MESH:D014777), chronic hepatitis (MESH:D006521), AISI (MESH:D007249), acute respiratory infections (MESH:D012141), thrombosis (MESH:D013927), microvascular occlusion (MESH:D017566), hyperlipidemia (MESH:D006949), rheumatoid arthritis (MESH:D001172), endothelial injury (MESH:D057772), central nervous system injury (MESH:D002493), infections (MESH:D007239), cardiovascular and inflammatory diseases (MESH:D002318), coagulation (MESH:D001778), CAP failure (MESH:D051437), cancer (MESH:D009369), ischemic stroke (MESH:D002544), diabetes (MESH:D003920), lymphopenia (MESH:D008231), post-stroke infection (MESH:D000094025), ischemic injury (MESH:D017202), endothelial dysfunction (MESH:D014652), ischemic (MESH:D002545), chronic obstructive pulmonary disease (MESH:D029424), systemic (MESH:D015619), atherosclerotic stroke (MESH:D002537), Stroke (MESH:D020521), TIA (MESH:D002546), inflammatory bowel disease (MESH:D015212), organ damage (MESH:D000092124), tissue damage (MESH:D017695), systemic lupus erythematosus (MESH:D008180), disability (MESH:D009069), CAP (MESH:C535672), neurological impairment (MESH:D009422), Coma (MESH:D003128), infectious diseases (MESH:D003141), sepsis (MESH:D018805), ischemia (MESH:D007511), neurological deficit (MESH:D009461), AIS (MESH:D000083242), acute (MESH:D000208)
- **Chemicals:** K (MESH:D011188), phosphate (MESH:D010710), TG (MESH:D013866), NA (MESH:D012964), TC (MESH:D013667), TG.HDL.LDL (-), triglyceride (MESH:D014280), lactate (MESH:D019344), urea (MESH:D014508), Mg (MESH:D008274), cholesterol (MESH:D002784), creatinine (MESH:D003404), chloride (MESH:D002712), reactive oxygen species (MESH:D017382)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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Source: https://tomesphere.com/paper/PMC12968109