Please cite this article as: LIU DS, LIU D, SONG HX, LI J, QIU MH, MA CQ, MU XF, ZHOU SX, DUAN YX, LI YY, LI Y, HAN YL. The systemic inflammatory response index as a risk factor for all-cause and cardiovascular mortality among individuals with coronary artery disease: evidence from the cohort study of NHANES 1999–2018. J Geriatr Cardiol 2025; 22(7): 668−677. DOI: 10.26599/1671-5411.2025.07.002.
Citation: Please cite this article as: LIU DS, LIU D, SONG HX, LI J, QIU MH, MA CQ, MU XF, ZHOU SX, DUAN YX, LI YY, LI Y, HAN YL. The systemic inflammatory response index as a risk factor for all-cause and cardiovascular mortality among individuals with coronary artery disease: evidence from the cohort study of NHANES 1999–2018. J Geriatr Cardiol 2025; 22(7): 668−677. DOI: 10.26599/1671-5411.2025.07.002.

The systemic inflammatory response index as a risk factor for all-cause and cardiovascular mortality among individuals with coronary artery disease: evidence from the cohort study of NHANES 1999–2018

  • Background The association of systemic inflammatory response index (SIRI) with prognosis of coronary artery disease (CAD) patients has never been investigated in a large sample with long-term follow-up. This study aimed to explore the association of SIRI with all-cause and cause-specific mortality in a nationally representative sample of CAD patients from United States.
    Methods A total of 3386 participants with CAD from the National Health and Nutrition Examination Survey (NHANES) 1999–2018 were included in this study. Cox proportional hazards model, restricted cubic spline (RCS), and receiver operating characteristic curve (ROC) were performed to investigate the association of SIRI with all-cause and cause-specific mortality. Piece-wise linear regression and sensitivity analyses were also performed.
    Results During a median follow-up of 7.7 years, 1454 all-cause mortality occurred. After adjusting for confounding factors, higher lnSIRI was significantly associated with higher risk of all-cause (HR = 1.16, 95% CI: 1.09–1.23) and CVD mortality (HR = 1.17, 95% CI: 1.05–1.30) but not cancer mortality (HR = 1.17, 95% CI: 0.99–1.38). The associations of SIRI with all-cause and CVD mortality were detected as J-shaped with threshold values of 1.05935 and 1.122946 for SIRI, respectively. ROC curves showed that lnSIRI had robust predictive effect both in short and long terms.
    Conclusions SIRI was independently associated with all-cause and CVD mortality, and the dose-response relationship was J-shaped. SIRI might serve as a valid predictor for all-cause and CVD mortality both in the short and long terms.
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