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Updated: Mar 15, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Vascular Function and Uric Acid-Lowering in Stage 3 CKD
Diana I Jalal1,2, Emily Decker1, Loni Perrenoud1
1Division of Renal Diseases and Hypertension, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado
Insights
Allopurinol effectively lowers serum uric acid in patients with stage 3 chronic kidney disease (CKD). However, this study found it did not improve endothelial dysfunction, despite a trend in non-diabetic participants.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Pharmacology
Background:
- Hyperuricemia is linked to endothelial dysfunction in chronic kidney disease (CKD).
- Targeting serum uric acid may offer a therapeutic strategy for CKD complications.
Purpose of the Study:
- To investigate if allopurinol reduces serum uric acid and improves endothelial function in stage 3 CKD patients.
- To assess the impact of allopurinol on blood pressure and markers of inflammation and oxidative stress.
Main Methods:
- A double-blind, placebo-controlled trial involving 80 adults with stage 3 CKD and asymptomatic hyperuricemia.
- Participants received either allopurinol or placebo for 12 weeks.
- Vascular endothelial function was measured using brachial artery flow-mediated dilation.
Main Results:
- Allopurinol significantly reduced serum uric acid levels compared to placebo.
- No significant improvement in endothelial function (flow-mediated dilation) was observed with allopurinol.
- A non-significant trend towards improved flow-mediated dilation was noted in participants without diabetes mellitus.
Conclusions:
- Allopurinol is effective and safe for lowering serum uric acid in stage 3 CKD patients with hyperuricemia.
- Allopurinol did not demonstrate a significant benefit in improving endothelial function in this patient cohort.
Abstract:
Hyperuricemia may contribute to endothelial dysfunction in CKD. We evaluated whether lowering serum uric acid levels with allopurinol improves endothelial dysfunction in 80 participants ≥18 years of age with stage 3 CKD and asymptomatic hyperuricemia (≥7 mg/dl in men and ≥6 mg/dl in women) randomized in a double-blinded manner to receive placebo or allopurinol for 12 weeks. Randomization was stratified according to presence or absence of diabetes mellitus. We measured vascular endothelial function by brachial artery flow-mediated dilation. No significant differences existed between groups at baseline; 61% of the participants had diabetes mellitus in both groups. The placebo and the allopurinol groups had baseline serum uric acid levels (SDs) of 8.7 (1.6) mg/dl and 8.3 (1.4) mg/dl, respectively, and baseline flow-mediated dilation values (SDs) of 6.0% (5.0%) and 4.8% (5.0%), respectively. Compared with placebo, allopurinol lowered serum uric acid significantly but did not improve endothelial function. In participants without diabetes mellitus, allopurinol associated with a trend toward improved flow-mediated dilation (+1.4% [3.9%] versus -0.7% [4.1%] with placebo), but this was not statistically significant (P=0.26). Furthermore, we did not detect significant differences between groups in BP or serum levels of markers of inflammation and oxidative stress. In conclusion, allopurinol effectively and safely lowered serum uric acid levels in adults with stage 3 CKD and asymptomatic hyperuricemia but did not improve endothelial function in this sample of patients.
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