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Uric acid levels and vascular disease
S S Daskalopoulou1, V G Athyros, M Elisaf
1Department of Clinical Biochemistry (Vascular Disease Prevention Clinics), Royal Free Hospital, Royal Free and University College Medical School, London, UK.
Insights
Serum uric acid (SUA) levels are linked to vascular event risk. Lowering SUA through common medications may significantly reduce vascular disease and mortality, supported by trial data.
Area of Science:
- Cardiology
- Vascular Medicine
- Pharmacology
Background:
- Serum uric acid (SUA) levels are recognized as a predictor of vascular events.
- Previous studies, such as the LIFE trial, suggest a link between reduced SUA and improved cardiovascular outcomes.
- The GREACE study also provides insights into the relationship between SUA levels and treatment strategies.
Purpose of the Study:
- To examine the SUA-lowering effects of commonly prescribed medications for vascular disease.
- To discuss how these reductions might impact vascular morbidity and mortality.
- To propose that judicious drug use can lead to significant reductions in vascular risk.
Main Methods:
- Review of findings from completed clinical trials, including the LIFE and GREACE studies.
- Discussion of the SUA-lowering effects of various drug classes (statins, fibrates, antihypertensives).
- Consideration of potential benefits from combining different therapeutic agents.
Main Results:
- Evidence suggests that SUA levels predict vascular event risk.
- A significant portion of outcome improvements in trials like LIFE can be attributed to SUA reduction.
- Commonly prescribed drugs, including statins and antihypertensives, can lower SUA levels.
Conclusions:
- Judicious use of medications, alone or in combination, can achieve modest reductions in SUA.
- These SUA reductions may translate into substantial decreases in vascular event risk.
- Further prospective studies are needed to confirm the association between SUA lowering and reduced vascular morbidity and mortality.
Abstract:
There is evidence showing that serum uric acid (SUA) levels predict the risk for vascular events. For example, up to 29% of the reduction in the primary composite endpoint seen in the LIFE trial (favouring losartan versus atenolol) can be attributed to a fall in SUA levels. We also discuss the findings of the GREACE study (treating to target with atorvastatin versus 'usual' care) in relation to SUA levels. In this brief comment we extend this argument to consider the SUA-lowering effect of other drugs commonly prescribed in patients with vascular disease (e.g. statins, fibrates and antihypertensive agents). A judicious use of drugs (alone or in combination) will result in small reductions in SUA levels. These changes may translate into a substantial reduction in the risk of vascular events. Results retrieved from completed trials together with new prospective findings will support or refute the proposed association between lowering SUA levels and reducing vascular morbidity and mortality.
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