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Clinical Implications of Uric Acid in Heart Failure: A Comprehensive Review
Marko Kumrić1, Josip A Borovac1,2, Tina Tičinović Kurir1,3
1Department of Pathophysiology, University of Split School of Medicine, 21000 Split, Croatia.
Insights
Uric acid (UA) is a key prognostic biomarker for heart failure (HF), predicting mortality and incidence. Emerging research suggests UA may also be a therapeutic target in HF management.
Area of Science:
- Cardiology
- Biomarkers
- Metabolic Syndrome
Background:
- Heart failure (HF) affects over 26 million globally, posing a significant health burden.
- Existing prognostic biomarkers for HF lack definitive clinical utility, necessitating cost-effective alternatives.
- Uric acid (UA), a product of purine metabolism, has a debated role in cardiovascular health.
Purpose of the Study:
- To review the prognostic significance of uric acid (UA) in heart failure (HF).
- To explore the potential of UA as a therapeutic target in HF.
- To discuss the role of UA and xanthine oxidase in HF pathogenesis.
Main Methods:
- Review of large population studies and emerging data on uric acid in HF.
- Analysis of UA as a predictor of mortality and incidence in acute and chronic HF.
- Discussion of xanthine oxidase's role and therapeutic implications in HF.
Main Results:
- Uric acid is an independent predictor of mortality in both acute and chronic heart failure.
- High serum UA levels are associated with an increased incidence of HF.
- Emerging evidence implicates UA in the pathogenesis of HF, suggesting it as a therapeutic target.
Conclusions:
- Uric acid demonstrates significant prognostic value in heart failure.
- UA's role in HF pathogenesis highlights its potential as a therapeutic target.
- Further research is needed to clarify the benefits of targeting UA and xanthine oxidase in HF patients.
Abstract:
Affecting more than 26 million people worldwide and with rising prevalence, heart failure (HF) represents a major global health problem. Hence, further research is needed in order to abate poor HF outcomes and mitigate significant expenses that burden health care systems. Based on available data, experts agree that there is an urgent need for a cost-effective prognostic biomarker in HF. Although a significant number of biomarkers have already been investigated in this setting, the clinical utility of adding biomarker evaluation to routine HF care still remains ambiguous. Specifically, in this review we focused on uric acid (UA), a purine metabolism detriment whose role as cardiovascular risk factor has been exhaustingly debated for decades. Multiple large population studies indicate that UA is an independent predictor of mortality in acute and chronic HF, making it a significant prognostic factor in both settings. High serum levels have been also associated with an increased incidence of HF, thus expanding the clinical utility of UA. Importantly, emerging data suggests that UA is also implicated in the pathogenesis of HF, which sheds light on UA as a feasible therapeutic target. Although to date clinical studies have not been able to prove the benefits of xanthine oxidase in HF patients, we discuss the putative role of UA and xanthine oxidase in the pathophysiology of HF as a therapeutic target.
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