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Updated: Jan 23, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Urate-lowering agents for asymptomatic hyperuricemia in stage 3 - 4 chronic kidney disease: Controversial role of
Hee Jung Jeon1, Jieun Oh1, Dong Ho Shin1
1Department of Internal Medicine, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Republic of Korea.
Insights
Pharmacologic urate-lowering therapy did not significantly impact kidney survival or slow disease progression in patients with stage 3-4 chronic kidney disease (CKD) and asymptomatic hyperuricemia. Further research is needed to confirm its efficacy.
Area of Science:
- Nephrology
- Internal Medicine
- Pharmacology
Background:
- Hyperuricemia is linked to chronic kidney disease (CKD) progression, but its causal role in asymptomatic patients is debated.
- Serum uric acid levels rise as glomerular filtration rate (GFR) declines, a hallmark of CKD.
Purpose of the Study:
- To investigate the effect of pharmacologic urate-lowering therapy on kidney survival and GFR decline in patients with stage 3-4 CKD and asymptomatic hyperuricemia.
Main Methods:
- Propensity score matching created 165 pairs of patients treated versus untreated with urate-lowering agents.
- Kaplan-Meier curves and Cox regression analyzed kidney survival.
- Linear mixed models assessed GFR changes over time.
Main Results:
- No significant difference in end-stage kidney disease (ESKD) incidence or kidney survival between treated and untreated groups.
- Pharmacologic urate-lowering therapy was not a predictor of kidney survival.
- Overall GFR decline rates were comparable between groups (P=0.13).
Conclusions:
- Pharmacologic urate-lowering therapy's efficacy in delaying CKD progression in this patient group remains controversial.
- Heart failure and low estimated GFR (eGFR) were significant prognostic factors for kidney survival.
- Further randomized controlled trials are necessary to confirm efficacy.
Abstract:
Because the serum uric acid level increases as the glomerular filtration rate (GFR) decreases, hyperuricemia is associated with chronic kidney disease (CKD). Although hyperuricemia is a risk factor for CKD progression, the causal role of uric acid remains controversial in patients with CKD and asymptomatic hyperuricemia. This study included 588 patients with stage 3-4 CKD and asymptomatic hyperuricemia. Using propensity score matching, 165 pairs treated and untreated with pharmacologic urate-lowering therapy were matched. Kaplan-Meier curves were constructed to determine the effect of urate-lowering agents on kidney survival. The prognostic value for kidney survival was ascertained using Cox regression analysis. The GFR changes over time between the patients treated and untreated with urate-lowering agents were assessed using a linear mixed model analysis. The mean age of the matched patients was 63.2 ± 12.7 years, and 52 (15.8%) patients had diabetic nephropathy. The mean estimated GFR (eGFR) and serum uric acid level were 36.7 mL/min/1.73 m2 and 7.8 mg/dL, respectively. During a mean follow-up period of 41.9 months, 87 developed end-stage kidney disease (ESKD). The incidence rates of ESKD were comparable between the patients treated and untreated with urate-lowering agents. The Kaplan-Meier analysis indicated that kidney survival was also comparable between them. In the multivariate analysis, heart failure and low eGFR were the significant prognostic factors for kidney survival. However, pharmacologic urate-lowering therapy was not predictive of kidney survival. The overall GFR decline rate was also comparable between the groups (P = 0.13). The efficacy of pharmacologic urate-lowering therapy in delaying CKD progression remains controversial. Therefore, further randomized controlled trials are needed to confirm its efficacy in attenuating kidney function deterioration in patients with stage 3-4 CKD.
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