Urate lowering agents don't slow progression of CKD in hyperuricemia, finds study
Hyperuricemia is very common in CKD patients because of reduced urinary excretion of uric acid. The role of uric acid in the development CKD and whether urate-lowering therapy (ULT) is warranted for its treatment are controversial issues.A new study by Xiang Liu, and team reported that febuxostat showed a tendency to be superior to allopurinol on lowering the decline of eGFR and increment...
Hyperuricemia is very common in CKD patients because of reduced urinary excretion of uric acid. The role of uric acid in the development CKD and whether urate-lowering therapy (ULT) is warranted for its treatment are controversial issues.
A new study by Xiang Liu, and team reported that febuxostat showed a tendency to be superior to allopurinol on lowering the decline of eGFR and increment of proteinturia, but showed lesser statistical significance. This study is published in Frontiers in Pharmacology.
The objective of the study was to summarize and compare the clinical outcomes and adverse events (AEs) of three common ULT drugs, we performed a systematic review and network meta-analysis of randomized clinical trials (RCTs).
The study used online platforms like PubMed, MEDLINE, Clinical Trials.gov, EMBASE, and the Cochrane Central Register of Controlled Trials electronic databases. The network meta-analysis was performed using the "gemtc 0.8-7" and its dependent packages in R software. The primary outcome was the change of renal function and uric acid; creatinine, proteinuria, blood pressure, and adverse events were assessed as the secondary outcomes.
The results of the study were found to be
• Out of 16 RCTs involving 1,943 patients were included in the final network analysis. Febuxostat, allopurinol, and benzbromarone were not found to exert superior effects over placebo upon renoprotective effect.
• With respect to lowering urate, the three drugs showed to be statistically superior to placebo, while febuxostat could better lower urate than allopurinol (MD: −1.547; 95% CrI: −2.473 to −0.626).
• It is also indicated that febuxostat was superior to placebo at controlling blood pressure, while no differences were observed when allopurinol and benzbromarone were compared to placebo. These results are stable in subgroup analysis.
Liu and team concluded that "There is insufficient evidence to support the renoprotective effects of the three urate-lowering agents in CKD patients with hyperuricemia; febuxostat shows a tendency to be superior to allopurinol on lowering the decline of eGFR and increment of proteinturia, but the difference does not reach a statistical significance. Regarding its urate-lowering effect, febuxostat appears to be a satisfactory alternative to allopurinol and benzbromarone, and can control blood pressure better."
For further information: Liu X, Qiu Y, Li D, Tan J, Liang X and Qin W. Effectiveness of drug treatments for lowering uric acid on renal function in patients with chronic kidney disease and hyperuricemia: a network meta-analysis of randomized controlled trials. Front. Pharmacol. 12:690557. https://doi.org/10.3389/fphar.2021.690557
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