Association Between Systemic Immune-Inflammation Index and Outcomes of Acute Myocardial Infarction: A Systemic Review and Meta-Analysis
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Published on: September 20, 2024
Wen Sun1, Zheye Chen2, Yi Luo1
1EICU, Changxing People's Hospital of Zhejiang, Huzhou City, China.
Insights
The systemic immune-inflammation index (SII) is linked to higher risks of major adverse cardiovascular events (MACE), contrast-induced nephropathy (CIN), and mortality in acute myocardial infarction (AMI) patients. This highlights SII as a potential prognostic marker.
Area of Science:
- Cardiology
- Biomarkers
- Inflammation
Background:
- The systemic immune-inflammation index (SII) is a marker reflecting systemic inflammation.
- Acute myocardial infarction (AMI) is a leading cause of cardiovascular mortality.
- Predictive markers for adverse outcomes in AMI are crucial for patient management.
Purpose of the Study:
- To evaluate the association between the systemic immune-inflammation index (SII) and the risk of major adverse cardiovascular events (MACE), contrast-induced nephropathy (CIN), and overall mortality in patients with acute myocardial infarction (AMI).
Main Methods:
- A systematic review and meta-analysis of observational studies was conducted using data from PubMed, EMBASE, Web of Science, and Scopus.
- Studies included adult patients with AMI, assessing the association of SII with MACE, CIN, and mortality.
- Random-effects models were used to calculate pooled relative risks (RR) with 95% confidence intervals (CI). Subgroup analyses and GRADE assessments were performed.
Main Results:
- Twenty-three studies were included in the analysis.
- Elevated SII was significantly associated with increased risks of MACE (RR 2.95), overall mortality (RR 2.59), and CIN (RR 4.58) in AMI patients.
- Publication bias was detected for MACE and overall mortality, but not for CIN. Associations remained consistent in subgroup analyses.
Conclusions:
- Higher systemic immune-inflammation index (SII) levels in patients with acute myocardial infarction (AMI) are associated with elevated risks of major adverse cardiovascular events (MACE), contrast-induced nephropathy (CIN), and overall mortality.
- The SII demonstrates potential as a valuable prognostic biomarker for predicting adverse outcomes in AMI patients.
- Further research may validate the clinical utility of SII in AMI risk stratification and management.
Abstract:
Objective: To assess the link between systemic immune-inflammation index (SII) and risk of major adverse cardiovascular events (MACE), contrast-induced nephropathy (CIN), and overall mortality in patients with acute myocardial infarction (AMI). Patients and Methods: Electronic search of PubMed, EMBASE, Web of Science, and Scopus databases was done for observational studies with the data on the association of SII and outcomes, such as MACE, and CIN in adult (≥18 y) patients with AMI. A random-effects model was used, and the pooled effect sizes were expressed as relative risk (RR) with corresponding 95% confidence intervals (CI). Subgroup analysis was conducted on the basis of the type of AMI (ST elevation myocardial infarction and non-ST elevation myocardial infarction), sample size (≥500 and <500), and study design. GRADE assessment was used to evaluate the certainty of the evidence. Results: The analysis included 23 studies. Most studies were conducted in China (n = 13), followed by Turkey (n = 10). Majority of the studies (n = 20) had a retrospective cohort design. Patients with high SII had increased risk of MACE (RR 2.95, 95% CI: 1.25, 6.99; n = 5, I2 = 97.5%), overall mortality (RR 2.59, 95% CI: 1.64, 4.07; n = 6, I2 = 58.0%), and CIN (RR 4.58, 95% CI: 3.44, 6.10; n = 4, I2 = 0.0%), compared with patients with lower SII. Egger's test detected publication bias for MACE (p = 0.047) and overall mortality (p = 0.012) but not for CIN. These associations remained valid in subgroup analysis. Conclusion: Findings suggest that higher SII in patients with AMI is associated with increased risks of MACE, CIN, and overall mortality. This underscores SII's potential as a prognostic marker in AMI.
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