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Updated: Dec 13, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Cardiac biomarkers of heart failure in chronic kidney disease
Xiaorong Han1, Shuai Zhang1, Zhongbo Chen1
1Department of Cardiovascular Centre, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
Insights
Heart failure biomarkers are challenging in chronic kidney disease (CKD) due to renal insufficiency. This review explores biomarker groups and suggests combining multiple biomarkers monitored over time for better clinical impact in CKD patients.
Area of Science:
- Cardiology
- Nephrology
- Biomarker Research
Background:
- Heart failure poses a significant risk to patients with chronic kidney disease (CKD).
- Traditional heart failure biomarkers are often unreliable in CKD patients due to impaired renal function.
- Accurate diagnosis and prognosis of heart failure in CKD require specialized biomarker approaches.
Purpose of the Study:
- To review existing and emerging heart failure biomarkers applicable to CKD patients.
- To discuss the challenges posed by renal insufficiency on biomarker interpretation.
- To highlight the need for adjusted biomarker thresholds and combination strategies.
Main Methods:
- Exploration of four major groups of heart failure biomarkers: myocardial stretch, myocyte injury, fibrosis/inflammation, and renal function.
- Review of classic biomarkers with adjusted critical values for glomerular filtration rate (GFR).
- Summary of recent research on novel biomarkers and future research directions.
Main Results:
- Biomarkers for myocardial stretch (e.g., BNP, NT-proBNP), myocyte injury (e.g., hsTnT), fibrosis/inflammation (e.g., sST2, Gal-3), and renal function (e.g., NGAL, KIM-1) were analyzed.
- Classic biomarkers require GFR-adjusted thresholds for reliable interpretation in CKD.
- Emerging biomarkers show promise but require further validation.
Conclusions:
- Interpreting heart failure biomarkers in CKD necessitates consideration of renal function.
- Combining multiple biomarkers and monitoring them longitudinally offers greater clinical utility than single measurements.
- Future research should focus on developing and validating novel biomarkers and combination strategies tailored for CKD populations.
Abstract:
Heart failure remains a continuing threat to patients with chronic kidney disease (CKD). Although various heart failure biomarkers have been applied for early detection, diagnosis and prognosis in CKD, these are easily affected by renal insufficiency thus limiting use in these patients. In this review, the major four groups of heart failure biomarkers are explored. These include those associated with: myocardial stretch, ie, brain natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP) and mid-regional proatrial natriuretic peptide (MR-proANP); myocyte injury, ie, high-sensitivity troponin T (hsTnT), heart-type fatty acid-binding protein (H-FABP); fibrosis, matrix remodelling and inflammation, ie, soluble growth stimulating gene 2 (sST2), galectin-3 (Gal-3), growth differentiation factor-15 (GDF-15); and renal function, ie, neutrophil gelatinase-associated lipocalin (NGAL) kidney injury molecule-1 (KIM-1), cystatin C (CysC), urinary sodium and urinary albumin. This review highlights classic heart failure biomarkers with critical values adjusted to glomerular filtration rate, summarizes research progress of new heart failure biomarkers and future research directions. Because diagnostic and prognostic usefulness of a single time point biomarker is limited, biomarkers should be combined and monitored at multiple times for optimal clinical impact.
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