Related Experiment Video
Updated: Apr 20, 2026

Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Usefulness of S100A12 as a prognostic biomarker for adverse events in patients with heart failure
Yun-Yun He1, Wei Yan2, Chun-Lei Liu2
1Department of Cardiology, Chinese PLA General Hospital, Beijing China; School of Medicine, Nankai University, Tianjin China.
Insights
Elevated S100A12 protein levels are linked to chronic heart failure (CHF) and predict major cardiovascular events (MCE) in patients. This finding highlights S100A12 as a potential biomarker for CHF prognosis.
Area of Science:
- Biochemistry
- Cardiology
- Immunology
Background:
- S100A12 protein is implicated in granulocyte-mediated inflammation.
- Chronic heart failure (CHF) is a significant cardiovascular condition with ongoing research into its underlying mechanisms and biomarkers.
Purpose of the Study:
- To investigate the association between S100A12 protein levels and chronic heart failure (CHF).
- To determine if S100A12 can serve as a predictive biomarker for major cardiovascular events (MCE) in CHF patients.
Main Methods:
- Plasma S100A12 and high-sensitivity C-reactive protein (hs-CRP) levels were measured in 177 CHF patients and 66 controls.
- CHF patients were followed for 18 months to record major cardiovascular events (MCE), including cardiac death and heart failure rehospitalization.
- Statistical analyses, including correlation and Cox regression, were employed to assess relationships and predictive value.
Main Results:
- Plasma S100A12 levels were significantly elevated in CHF patients compared to controls (P<0.001).
- S100A12 levels positively correlated with hs-CRP (r=0.316, P<0.001).
- Higher S100A12 levels were associated with an increased risk of MCE in CHF patients, with S100A12 identified as an independent risk factor (P=0.009).
Conclusions:
- S100A12 is a potential biomarker for chronic heart failure (CHF).
- S100A12 levels provide valuable information for predicting major cardiovascular events (MCE) in patients with CHF.
Objectives:
S100A12 has been proposed as a novel pivotal factor in inflammation produced by granulocytes. The purpose of this study was to investigate the relationship between S100A12 and chronic heart failure (CHF).
Design And Methods:
One hundred and seventy-seven patients with CHF and 66 subjects without CHF were included in this study. Plasma levels of S100A12 and high-sensitivity C-reactive protein (hs-CRP) were measured in all participants. After a follow-up period of 18months for CHF patients, major cardiovascular events (MCE), including cardiac death and rehospitalization for heart failure, were recorded.
Results:
Plasma levels of S100A12 were significantly higher in CHF patients than in control subjects (P<0.001) and positively correlated with hs-CRP (r=0.316, P<0.001). S100A12 levels were also higher in MCE patients than in MCE-free patients. The occurrence of MCE increased with advancing plasma S100A12 levels by stratification according to quartiles (Q4 vs Q1, P=0.015). Cox proportional hazards regression analysis revealed that S100A12 was an independent risk factor for MCE in CHF patients (P=0.009).
Conclusions:
S100A12 is a potential biomarker of CHF that may provide important information regarding the prediction of MCE in patients with CHF.
Related Concept Videos
Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers
These markers indicate stress or strain on the heart muscle:
Natriuretic Peptides (BNP)
Cardiac myocytes produce these hormones in response to ventricular stretching...
Blood Studies for Cardiovascular System I: Cardiac Biomarkers
The essential diagnostic tools for detecting myocardial necrosis and monitoring individuals suspected of having acute coronary syndrome (ACS) include:
Troponins
Troponins, particularly cardiac troponins I and T, are the most precise and sensitive markers of myocardial injury. They are detectable within 4-6 hours of myocardial injury and remain...
Acute Coronary Syndrome III: Diagnostic Studies
Heart Failure II: Pathophysiology
