Key result
Higher systemic immune-inflammation index is linked to more severe coronary stenosis in males with ACS.
Why the study?
Elevated systemic immune-inflammation index (SII) correlates with CAD prevalence and severity in ACS, prompting evaluation of the influence of sex on SII and its association with coronary stenosis.
Cross-Sectional (n=130)
Single-blind (coronary angiography results independently evaluated by two cardiovascular experts blinded to clinical data)
No
Answers are grounded in this paper and cite their sources.
The systemic immune-inflammation index (SII) is independently associated with the severity of coronary artery stenosis in male patients with acute coronary syndrome, but not in female patients, highlighting the need to account for sex differences when using inflammatory biomarkers for risk stratification.
BACKGROUND: Elevated systemic immune-inflammation index (SII) correlates with increased coronary artery disease (CAD) prevalence and severity in acute coronary syndrome (ACS). The aim of this study was to evaluate the influence of sex on SII and its association with coronary stenosis in ACS. METHODS: A total of 130 patients with ACS, who had performed coronary angiography, were enrolled. Gensini Score (GS) was used to reflect the degree of coronary stenosis. The association of SII and GS were studied. RESULTS: The mean values of SII and GS were significantly higher (p = 0.048 and 0.001, respectively) in male individuals compared with female counterparts. There was a significant correlation between SII and GS (r = 0.306, p = 0.006) in male participants. However, the positive correlation between SII and GS was not found in female subjects. SII was independently associated with GS (B = 0.030, p = 0.007) after controlling for age, smoking, and low-density lipoprotein cholesterol (LDL-C) in male participants. LDL-C (B = 11.741, p = 0.003), smoking (B = 39.018, p = 0.016) and age (B = 1.139, p = 0.030), but not SII (B = 0.027, p = 0.101) were found to be independently correlated with the degree of coronary stenosis in females. CONCLUSIONS: SII was a associated marker for evaluating the extent of coronary lesions in male subjects with ACS, but not in female counterparts.
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Hong et al. (2026) conducted a cross-sectional in Acute coronary syndrome (ACS) (n=130). Systemic immune-inflammation index (SII) stratified by sex vs. Female patients with ACS (N=50) vs Male patients with ACS (N=80) was evaluated on Degree of coronary artery stenosis quantified by the Gensini Score (GS) (B = 0.030 (in males), 95% CI 0.009 to 0.052, p=0.007). Systemic immune-inflammation index was independently associated with coronary stenosis severity (Gensini Score) in males with ACS (B=0.030, p=0.007), but not in females (B=0.027, p=0.101).
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