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Published on: January 28, 2020
Association of Systemic Inflammation Indices With Mortality in Coronary Atherosclerosis Patients With and Without
Weiren Yan1, Bingqian Zhang1, Xiaoyan Zhang2
1Department of Cardiology, The First Affiliated Hospital of Dalian Medical University, Dalian, China, dlmedu.edu.cn.
Insights
Inflammation markers, systemic immune inflammatory index (SII) and systemic inflammatory response index (SIRI), predict mortality in coronary heart disease (CHD) patients, regardless of standard modifiable risk factors (SMuRFs). Higher SII and SIRI levels are linked to increased all-cause mortality in both SMuRF-present and SMuRF-less CHD groups.
Area of Science:
- Cardiovascular Medicine
- Inflammation Research
- Public Health Epidemiology
Background:
- Standard modifiable risk factors (SMuRFs) are key drivers of coronary atherosclerosis.
- A subset of individuals develop coronary atherosclerosis without identifiable SMuRFs, suggesting alternative etiological pathways.
- Inflammation is recognized as a significant contributor to atherosclerosis development and progression.
Purpose of the Study:
- To investigate the association between novel inflammatory markers, systemic immune inflammatory index (SII) and systemic inflammatory response index (SIRI), and mortality in coronary heart disease (CHD) patients.
- To examine these associations separately in patients with and without SMuRFs.
- To explore the role of inflammation as a potential driver of poor prognosis in SMuRF-less CHD patients.
Main Methods:
- Analysis of 1708 CHD participants from the National Health and Nutrition Examination Survey (NHANES) (1999-2018).
- Categorization of participants into '≥1 SMuRF' and 'SMuRF-less' groups based on questionnaires and serologic testing.
- Assessment of mortality risk using multivariate weighted Cox regression and restricted cubic spline (RCS) analysis for SII and SIRI, stratified by SMuRF status.
Main Results:
- In patients with ≥1 SMuRF, higher quartiles of SII and SIRI were significantly associated with increased all-cause and cardiovascular mortality.
- In SMuRF-less patients, elevated SII and SIRI levels were significantly linked to higher all-cause mortality, with SIRI also showing a significant association with cardiovascular mortality.
- RCS analysis revealed a positive linear trend between higher SII/SIRI levels and all-cause mortality in both SMuRF groups, and cardiovascular mortality in the SMuRF-present group.
Conclusions:
- SII and SIRI are independently associated with all-cause mortality in CHD patients, irrespective of SMuRF status.
- Inflammation, as indicated by SII and SIRI, may play a crucial role in the adverse outcomes of patients with CHD, particularly those lacking traditional risk factors.
- Further prospective studies are warranted to confirm these findings and elucidate the underlying mechanisms.
Background:
Standard modifiable risk factors (SMuRFs) are important causative factors leading to coronary atherosclerosis. However, a significant number of individuals develop coronary atherosclerosis despite the absence of SMuRFs. Inflammation is another major cause of atherosclerosis, and this study aims to investigate the association of the novel inflammatory markers systemic immune inflammatory index (SII) and systemic inflammatory response index (SIRI) with mortality in patients with coronary heart disease (CHD) with and without SMuRFs.
Methods:
In this study, we included 1708 CHD participants from the 1999-2018 National Health and Nutrition Examination Survey (NHANES). Patients were categorized into ≥ 1SMuRF and SMuRF-less groups by questionnaire and serologic testing. SII and SIRI were categorized into four groups according to quartiles. Multivariate weighted Cox regression was used to explore the risk factors associated with mortality in patients with or without SMuRFs. Restricted cubic spline (RCS) curve was used to assess their nonlinear correlation.
Results:
In patients with ≥1 SMuRF, all-cause mortality (SII:hazard ratio [HR] 1.47, 95% confidence interval [CI] 1.18-1.84, p < 0.001; SIRI:HR 1.66, 95%CI 1.31-2.10, p < 0.001) and cardiovascular mortality (SII:HR 1.52, 95%CI 1.07-2.17, p = 0.020; SIRI:HR 1.63, 95%CI 1.11-2.38, p = 0.011) were significantly higher in the SII Q4 and SIRI Q4 group compared to the SII Q1 and SIRI Q1 group, respectively. In patients with SMuRF-less, the incidence of all-cause mortality was also significantly higher in the group with higher levels of SII, SIRI (SII:HR 3.32, 95%CI 1.45-7.59, p = 0.004; SIRI:HR 4.25, 95%CI 1.67-10.80, p = 0.002), but no significant difference was observed in cardiovascular mortality for SII (SII:HR 2.21, 95%CI 0.54-8.97, p = 0.272), while a significant association was found for SIRI (SIRI:HR 11.69, 95%CI 1.43-95.21, p = 0.028). The RCS analysis showed a linear trend between high levels of SII, SIRI, and elevated all-cause mortality, and cardiovascular mortality in patients with ≥1 SMurRF. In contrast, a positive linear trend between SII, SIRI, and all-cause mortality, but no significant association with cardiovascular mortality was observed in the group with SMuRF-less.
Conclusions:
The findings showed that SII and SIRI were positively associated with all-cause mortality in a population with CHD irrespective of the presence or absence of SMuRFs. The present study suggests that inflammation may be an important factor in the poor prognosis of patients with no specific cardiovascular risk factors, which needs to be further argued by more prospective studies.
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