# Association between the systemic inflammation response index and the prognosis of patients with myocardial infarction: a systematic review and meta-analysis

**Authors:** Yedan Wu, Rong Zheng, Yuling Lin, Zhiqing Shen, Hong Shi

PMC · DOI: 10.3389/fcvm.2026.1755442 · Frontiers in Cardiovascular Medicine · 2026-02-16

## TL;DR

This study finds that higher systemic inflammation response index (SIRI) is linked to worse outcomes in heart attack patients, suggesting SIRI could help predict risks.

## Contribution

The study is the first to systematically evaluate SIRI as a prognostic biomarker in myocardial infarction patients using a meta-analysis.

## Key findings

- Elevated SIRI is associated with increased risk of major adverse cardiovascular events (OR = 1.42).
- Higher SIRI correlates with increased all-cause mortality (OR = 1.28) and stroke (OR = 1.11).
- SIRI is strongly linked to higher Gensini scores (OR = 6.89), indicating more severe coronary artery disease.

## Abstract

The systemic inflammation response index (SIRI), a novel biomarker integrating neutrophil, monocyte, and lymphocyte counts, has been implicated in cardiovascular disease prognosis. This study aimed to systematically evaluate the association between SIRI and clinical outcomes in patients with myocardial infarction (MI).

A comprehensive literature search was conducted across multiple databases up to July 2025. Observational studies reporting odds ratios (ORs) with 95% confidence intervals (CIs) for the association between SIRI and post-MI outcomes were included. Pooled ORs were calculated using random-effects models. Heterogeneity and publication bias were assessed.

Twelve comparative groups (6,751 participants) showed that elevated SIRI was possibly associated with an increased risk of major adverse cardiovascular events (MACE) (OR = 1.42, 95% CI: 1.27–1.58). SIRI was also potentially associated with higher all-cause mortality (OR = 1.28), stroke (OR = 1.11), subsequent AMI (OR = 1.21), and the Gensini score (OR = 6.89). Significant heterogeneity was observed for some outcomes. Subgroup analyses indicated that study sample size and SIRI cut-off values were potential sources of heterogeneity.

An elevated SIRI is consistently associated with an increased risk of adverse clinical outcomes in patients with MI, underscoring its potential value as a readily accessible prognostic biomarker for risk stratification.

https://www.crd.york.ac.uk/PROSPERO/, identifier CRD420251169048.

## Linked entities

- **Diseases:** myocardial infarction (MONDO:0005068), stroke (MONDO:0005098)

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}
- **Diseases:** ACS (MESH:D000168), Cardiovascular Strokes (MESH:D009203), Cardiovascular Events (MESH:D002318), MINOCA (MESH:D000088442), acute coronary syndrome (MESH:D054058), ASCVD (MESH:D050197), Inflammation (MESH:D007249), pericarditis (MESH:D010493), reperfusion injury (MESH:D015427), stent thrombosis (MESH:D013927), atherosclerotic plaque (MESH:D058226), myocardial injury (MESH:D009202), stroke (MESH:D020521), CAD (MESH:D003324), STEMI (MESH:D000072657), infarction (MESH:D007238), heart failure (MESH:D006333), arrhythmias (MESH:D001145), bleeding (MESH:D006470)
- **Chemicals:** ROS (MESH:D017382), lipids (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12950576/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950576/full.md

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Source: https://tomesphere.com/paper/PMC12950576