Key result
High systemic immune-inflammation index linked to ~65% greater MACCE risk.
Why the study?
The prognostic value of the systemic immune inflammation index (SII) for long-term outcomes in patients with three-vessel disease after revascularization was unknown.
Does a high systemic immune-inflammation index predict increased risk of MACCE and all-cause death in patients with three-vessel coronary disease after revascularization?
Cohort (n=3,561)
Does a high systemic immune-inflammation index predict increased risk of MACCE and all-cause death in patients with three-vessel coronary disease after revascularization?
Effect estimate: HR 1.65 (95% CI 1.23-2.21)
p-value: p=0.001
A high systemic immune-inflammation index (≥ 694.3 × 10^9 /L) is an independent predictor of MACCE and all-cause death in patients with three-vessel coronary disease following revascularization, improving risk stratification beyond traditional factors.
May refine post-revascularization prognostication in three-vessel disease; leaves open causal role and therapeutic targeting of systemic inflammation.
Objective: This study aimed to investigate the prognostic value of systemic immune inflammation index (SII) concerning long-term outcomes in patients with the three-vessel disease (TVD) after revascularization in a large cohort. Methods: In total, 3561 TVD patients who had undergone revascularization between 2013 and 2018 were included in the study. Patients were divided into the low SII (< 694.3 × 10 9 /L) (n = 2556, 71.8%) and the high SII (≥ 694.3 × 10 9 /L) group (n = 1005, 28.2%). The C-index, net reclassification improvement (NRI), and integrated discrimination improvement (IDI) were calculated to assess whether the addition of SII to a baseline model with traditional risk factors improved the accuracy of cardiac event prediction. The primary outcome was the frequency of major adverse and cerebrovascular events (MACCE). The secondary outcome was the incidence of all-cause death. Results: After 2.4 years of follow-up, the Cox proportional hazard regression model analysis displayed that high SII was independently associated with an increased risk of developing future MACCE (hazard ratio [HR] 1.65, 95% confidence interval [CI] 1.23– 2.21, p = 0.001) and all-cause death (HR: 2.96; 95% CI: 1.19– 7.32, p = 0.019). The addition of SII significantly improved the reclassification beyond the baseline model with traditional risk factors (MACCE: NRI, 0.115; p = 0.0001; all-cause death: NRI, 0.369; p = 0.0001). Reclassification with the addition of SII also demonstrated an IDI of 0.0022 (p = 0.006) in MACCE and 0.0033 (p = 0.014) in all-cause death. Conclusion: In TVD patients after revascularization, increased SII is an independent prognostic factor for long-term outcomes of MACCE and death. Compared to traditional risk factors, SII improved the risk prediction of major cardiovascular events in TVD patients who underwent revascularization.
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Zhao et al. (2022) conducted a cohort in Three-vessel coronary disease after revascularization (n=3,561). High systemic immune-inflammation index (≥ 694.3 × 10^9/L) vs. Low systemic immune-inflammation index (< 694.3 × 10^9/L) was evaluated on Major adverse and cerebrovascular events (MACCE) (HR 1.65, 95% CI 1.23-2.21, p=0.001). A high systemic immune-inflammation index (≥694.3 × 10^9/L) was associated with an increased risk of MACCE compared to a low index (HR 1.65; 95% CI 1.23-2.21; p=0.001).
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