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Updated: Feb 15, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
[Hyperuricaemia and Chronic Kidney Disease]
Carlo Garofalo1, Toni De Stefano1, Carlo Vita1
1Cattedra di Nefrologia-Università degli studi della Campania "Luigi Vanvitelli"; P.O. S.M.d.P. Incurabili, Napoli.
High serum uric acid (hyperuricemia) is linked to cardiovascular disease and chronic kidney disease. Febuxostat shows promise in managing hyperuricemia, with ongoing studies evaluating its kidney-protective effects.
Area of Science:
- Nephrology
- Cardiology
- Metabolic Disorders
Background:
- Hyperuricemia, defined as serum uric acid > 6 mg/dl, results from overproduction or reduced renal excretion.
- Prevalence in Italy is ~12%, rising to 60% in renal disease patients.
- Uric acid is implicated in arterial hypertension, arteriosclerosis, and increased cardiovascular risk.
Purpose of the Study:
- To review the role of hyperuricemia in cardiovascular and kidney disease.
- To compare febuxostat with allopurinol for hyperuricemia management.
- To discuss the potential of urate-lowering therapy in reducing cardiovascular events and slowing chronic kidney disease progression.
Main Methods:
- Review of experimental and observational studies.
- Analysis of randomized controlled trials (RCTs) comparing febuxostat and allopurinol.
- Discussion of ongoing RCTs focused on nephroprotective effects of urate-lowering treatments.
Main Results:
- Febuxostat demonstrated superior hyperuricemia control compared to allopurinol in RCTs.
- Observational studies suggest urate-lowering treatment may reduce cardiovascular events.
- Urate-lowering therapies may slow the progression of chronic kidney disease.
Conclusions:
- Hyperuricemia is an independent risk factor for de novo chronic kidney disease.
- Febuxostat offers effective hyperuricemia management.
- Further research, including ongoing RCTs, is needed to confirm the nephroprotective benefits of urate-lowering treatments.
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