Exploration of the Potential Biomarker FNDC5 for Discriminating Heart Failure in Patients with Coronary Atherosclerosis
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Updated: Jul 2, 2025

Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Hongchao Zheng1, Yuntao Zheng2, Wei Huang2
1Biomarker Exploring Program, Shanghai Xuhui Central Hospital/Zhongshan-Xuhui Hospital, Fudan University, 966 Middle Huaihai Road, Shanghai, 200031, China.
Insights
Fibronectin type III domain containing 5 (FNDC5) and B-type natriuretic peptide (BNP) can help identify heart failure (HF) in patients with coronary atherosclerosis. Reduced FNDC5 and elevated BNP levels indicate HF risk.
Area of Science:
- Cardiology
- Biomarker Discovery
- Atherosclerosis Research
Background:
- Coronary atherosclerosis is a primary cause of ischemic heart disease and subsequent heart failure (HF).
- Identifying reliable biomarkers for early HF detection in atherosclerotic patients is crucial for timely intervention.
- Current diagnostic methods may require enhancement for precise HF discrimination in this population.
Purpose of the Study:
- To investigate novel biomarkers for differentiating heart failure (HF) in patients diagnosed with coronary atherosclerosis.
- To assess the potential of B-type natriuretic peptide (BNP), fibronectin type III domain containing 5 (FNDC5), and Phosphodiesterase 9A (PDE9A) as HF discriminators.
- To evaluate the correlation and diagnostic value of these biomarkers in atherosclerotic individuals with and without HF.
Main Methods:
- Study included 40 consecutive atherosclerotic patients undergoing angiography.
- Assessed serum concentrations of BNP, FNDC5, and PDE9A in 20 HF patients and 20 non-HF controls.
- Employed Pearson correlation and Receiver Operating Characteristics (ROC) analysis to evaluate biomarker performance.
Main Results:
- Elevated circulating BNP levels were observed in atherosclerotic patients with HF symptoms/signs.
- Reduced FNDC5 levels were detected in atherosclerotic patients presenting with HF symptoms/signs.
- Pearson correlation revealed a significant association between FNDC5 and BNP; ROC analysis confirmed their ability to discriminate HF.
Conclusions:
- FNDC5 and BNP show independent value as biomarkers for discriminating heart failure in patients with coronary atherosclerosis.
- The combined assessment of FNDC5 and BNP may improve HF diagnosis accuracy in this cohort.
- Further research into FNDC5's role in HF pathogenesis within atherosclerotic disease is warranted.
Abstract:
Coronary atherosclerosis leading to ischemic artery disease is one of the etiological factors to develop heart failure (HF). This study aimed to investigate potential biomarkers for discriminating HF in atherosclerotic patients. This study included 40 consecutive atherosclerotic patients who underwent angiography. Concentrations of B-type natriuretic peptide (BNP), fibronectin type III domain containing 5 (FNDC5), and Phosphodiesterase 9A (PDE9A) were measured in 20 atherosclerotic patients with HF symptoms/signs and 20 without HF symptoms/signs. Circulating BNP levels were elevated, while FNDC5 levels were reduced in atherosclerotic patients with HF symptoms/signs compared to those without HF symptoms/signs. Pearson correlation analysis showed a significant correlation between FNDC5 and BNP. Receiver Operating Characteristics analysis indicated that both FNDC5 and BNP were able to discriminate HF in atherosclerotic patients. Our findings suggest that FNDC5, along with BNP, has independent value as a biomarker for discriminating HF in patients with coronary atherosclerosis.
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