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Published on: January 28, 2020
Association between inflammatory burden index and prognosis in patients with coronary heart disease: A retrospective
Wen Lu1, Xiaoqin Liao2,3, Yan Jiang1
1School of Nursing, Fujian Medical University, Fuzhou, Fujian, China.
Insights
The inflammatory burden index (IBI) is a novel biomarker indicating higher risks for adverse outcomes in coronary heart disease (CHD) patients. Higher IBI levels are linked to increased major adverse cardiovascular and cerebrovascular events (MACCEs).
Area of Science:
- Cardiology
- Biomarkers
- Systemic Inflammation
Background:
- Systemic inflammation is a significant factor in the adverse prognosis of coronary heart disease (CHD).
- The inflammatory burden index (IBI) is a novel biomarker reflecting systemic inflammation.
- Investigating the association between IBI and CHD patient prognosis is crucial.
Purpose of the Study:
- To investigate the association between the inflammatory burden index (IBI) and the prognosis of coronary heart disease (CHD) patients.
- To determine if IBI can predict adverse cardiovascular and cerebrovascular events (MACCEs) in CHD patients.
- To explore the relationship between IBI levels and specific adverse outcomes like new-onset atrial fibrillation (NOAF) and contrast-induced nephropathy (CIN).
Main Methods:
- Retrospective analysis of 2453 CHD patients from December 2017 to December 2022.
- IBI calculated as neutrophil/lymphocyte*C-reactive protein, with patients grouped by baseline IBI quartiles.
- Multivariate logistic regression and restricted cubic spline (RCS) analysis used to assess IBI's predictive value for MACCEs, NOAF, and CIN.
Main Results:
- Higher IBI levels, particularly IBI ≥ 45.68, were associated with an increased risk of MACCEs.
- Baseline IBI independently predicted new-onset atrial fibrillation (NOAF) (OR: 2.05) and contrast-induced nephropathy (CIN) (OR: 1.95) in CHD patients.
- RCS analysis confirmed a linear relationship between IBI and NOAF, and a nonlinear relationship with CIN.
Conclusions:
- The inflammatory burden index (IBI) is a promising biomarker for systemic inflammation in CHD patients.
- Elevated IBI levels are associated with an adverse prognosis and increased risk of MACCEs.
- These findings support the use of IBI for precise clinical decision-making to improve CHD patient outcomes.
Background:
Increasing evidences indicate that systemic inflammation plays a significant role of adverse prognosis in patients with coronary heart disease (CHD). The inflammatory burden index (IBI) is a novel biomarker that reflects systemic inflammation. The aim of this study was to investigate the association between IBI and prognosis of CHD patients.
Methods:
In this retrospective analysis, data from 2453 CHD patients enrolled from December 2017 to December 2022.IBI was defined as neutrophil/lymphocyte*C-reactive protein, with patients categorized into four groups based on quartiles of baseline IBI levels. The primary outcome was adverse cardiovascular and cerebrovascular events (MACCEs) occurring during hospitalization, which included repeat revascularization, new-onset atrial fibrillation (NOAF), stroke, and all-cause in-hospital mortality. Multivariate logistic regression models and restricted cubic spline (RCS) analysis were used to investigate the association between IBI and prognosis of CHD patients.
Results:
High levels of IBI were associated with higher risk of MACCEs, especially when IBI ≥ 45.68, patients exhibited a higher risk of MACCEs (P < 0.05). After adjusting for baseline confounders, multivariate logistic regression analysis demonstrated that baseline IBI was an independent predictor for NOAF (Odds Ratio (OR): 2.05; 95% confidence interval (CI): 1.30-3.24; P = 0.002) and contrast-induced nephropathy (CIN) (OR: 1.95; 95%CI: 1.16-3.28; P = 0.012) in CHD patients, mainly driven by the highest quartile. In addition, RCS confirmed a linear relationship between IBI and NOAF (P for non-linear = 0.425) and a nonlinear relationship with CIN (P for non-linear = 0.032).
Conclusion:
IBI is a promising biomarker of systemic inflammation in CHD patients, where higher IBI levels are associated with adverse prognosis. These findings may aid clinicians in precise decision-making to improve outcomes in patients with CHD.
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