High Systemic Immune-Inflammatory Index (OR 3.102) and low Geriatric Nutritional Risk Index (OR 2.863) independently predicted an increased risk of major adverse cardiovascular events within one year in elderly patients with acute coronary syndromes.
Observational (n=827)
No
Does the combination of Geriatric Nutritional Risk Index (GNRI) and Systemic Immune-Inflammatory Index (SII) predict the risk of major adverse cardiovascular events within one year in elderly patients undergoing PCI for acute coronary syndromes?
Combining the Geriatric Nutritional Risk Index (GNRI) and Systemic Immune-Inflammatory Index (SII) provides a simple, cost-effective model that outperforms the GRACE score in predicting 1-year MACE risk in elderly ACS patients after PCI.
Odds Ratio: 3.102 (95% CI 2.213–4.348)
p-value: p=0.001
The objective of this study was to evaluate the predictive value of the Geriatric Nutritional Risk Index (GNRI) combined with the Systemic Immunoinflammatory Index (SII) for the risk of major adverse cardiovascular events (MACE) following percutaneous coronary intervention in elderly patients with acute coronary syndrome (ACS). We retrospectively reviewed the medical records of 1202 elderly patients with acute coronary syndromes divided into MACE and non-MACE groups according to whether they had a MACE. The sensitivity analysis utilized advanced machine learning algorithms to preliminarily identify the critical role of GNRI versus SII in predicting MACE risk. We conducted a detailed analysis using a restricted cubic spline approach to investigate the nonlinear relationship between GNRI, SII, and MACE risk further. We constructed a clinical prediction model based on three key factors: GNRI, SII, and Age. To validate the accuracy and usefulness of this model, we compared it to the widely used GRACE score using subject work and recall curves. Additionally, we compared the predictive value of models and GRACE scores in assessing the risk of MACE using the Integrated Discriminant Improvement Index (IDI) and the Net Reclassification Index (NRI). This study included 827 patients. The GNRI scores were lower in the MACE group than in the non-MACE group, while the SII scores were higher in the MACE group (P < 0.001). The multifactorial analysis revealed a low GNRI (OR = 2.863, 95% CI: 2.026-4.047, P = 0.001), High SII (OR = 3.102, 95% CI: 2.213-4.348, P = 0.001). The area under the curve (AUC) for the predictive model was 0.778 (95% CI: 0.744-0.813, P = 0.001), while the AUC for the GRACE score was 0.744 (95% CI: 0.708-0.779, P = 0.001). NRI was calculated to be 0.5569, with NRI + at 0.1860 and NRI- at 0.3708. The IDI was found to be 0.0571, with a P-value of less than 0.001. These results suggest that the newly developed prediction model is more suitable for use with the population in this study than the GRACE score. The model constructed using GNRI and SII demonstrated good standardization and clinical impact, as evidenced by the standard, DCA, and clinical impact curves. The study shows that combining GNRI and SII can be a simple, cost-effective, and valuable way to predict the risk of MACE within one year in elderly acute coronary syndromes.
Zhu et al. (Wed,) conducted a observational in Acute coronary syndromes (n=827). High Systemic Immune-Inflammatory Index (SII) vs. Low Systemic Immune-Inflammatory Index was evaluated on Major adverse cardiovascular events (MACE) within 1 year (OR 3.102, 95% CI 2.213-4.348, p=0.001). High Systemic Immune-Inflammatory Index (OR 3.102) and low Geriatric Nutritional Risk Index (OR 2.863) independently predicted an increased risk of major adverse cardiovascular events within one year in elderly patients with acute coronary syndromes.