» Articles » PMID: 37864678

Efficacy of Dotinurad in Patients with Severe Renal Dysfunction

Overview
Publisher Springer
Specialty Nephrology
Date 2023 Oct 21
PMID 37864678
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Although hyperuricemia is associated with the progression of chronic kidney disease (CKD), a reduction in CKD progression by uric acid (UA)-lowering therapy has been controversial. Recently, dotinurad, a uricosuric drug with selective urate reabsorption inhibitory properties, has been developed. However, its efficacy in lowering serum UA levels and its effects on renal function in patients with severe renal dysfunction are unclear. Thus, this study aimed to determine the effects of dotinurad on renal function in patients with severe renal dysfunction.

Methods: Data from 53 outpatients with hyperuricemia who newly received dotinurad between December 2020 and October 2022 were retrospectively analyzed. The mean baseline estimated glomerular filtration rate (eGFR) was 38.7 ± 17.0 mL/min/1.73 m. The patients were divided into three groups based on their baseline eGFR: eGFR < 30 (n = 17), 30 ≤ eGFR < 45 (n = 17), and eGFR ≥ 45 (n = 19).

Results: The mean follow-up period was 9.8 ± 4.5 (range, 3-21) months. Serum UA levels significantly decreased in all groups. Although eGFR did not significantly change in patients with 30 ≤ eGFR < 45 and eGFR ≥ 45 (P = 0.918 and P = 0.535, respectively), it improved significantly in patients with eGFR < 30 (P = 0.032). The proportion of patients with improved eGFR was significantly higher in patients with eGFR < 30 (P = 0.038) than in patients with 30 ≤ eGFR < 45 and eGFR ≥ 45. In the multivariate logistic regression analysis, baseline eGFR < 30 and achieving a serum UA level of ≤ 6.0 mg/dL were significantly associated with improved eGFR (P = 0.033 and P = 0.015, respectively).

Conclusions: Dotinurad may have UA-lowering effects and the potential to improve kidney function in patients with severe renal dysfunction.

Citing Articles

Comparative assessment of the effects of dotinurad and febuxostat on the renal function in chronic kidney disease patients with hyperuricemia.

Takata T, Taniguchi S, Mae Y, Kageyama K, Fujino Y, Iyama T Sci Rep. 2025; 15(1):8990.

PMID: 40089552 DOI: 10.1038/s41598-025-94020-2.


A Possible Therapeutic Application of the Selective Inhibitor of Urate Transporter 1, Dotinurad, for Metabolic Syndrome, Chronic Kidney Disease, and Cardiovascular Disease.

Yanai H, Adachi H, Hakoshima M, Iida S, Katsuyama H Cells. 2024; 13(5.

PMID: 38474414 PMC: 10931163. DOI: 10.3390/cells13050450.

References
1.
Chen J, Chuang S, Chen H, Yeh W, Pan W . Serum uric acid level as an independent risk factor for all-cause, cardiovascular, and ischemic stroke mortality: a Chinese cohort study. Arthritis Rheum. 2009; 61(2):225-32. DOI: 10.1002/art.24164. View

2.
Storhaug H, Norvik J, Toft I, Eriksen B, Lochen M, Zykova S . Uric acid is a risk factor for ischemic stroke and all-cause mortality in the general population: a gender specific analysis from The Tromsø Study. BMC Cardiovasc Disord. 2013; 13:115. PMC: 4029378. DOI: 10.1186/1471-2261-13-115. View

3.
Bos M, Koudstaal P, Hofman A, Witteman J, Breteler M . Uric acid is a risk factor for myocardial infarction and stroke: the Rotterdam study. Stroke. 2006; 37(6):1503-7. DOI: 10.1161/01.STR.0000221716.55088.d4. View

4.
Zhu P, Liu Y, Han L, Xu G, Ran J . Serum uric acid is associated with incident chronic kidney disease in middle-aged populations: a meta-analysis of 15 cohort studies. PLoS One. 2014; 9(6):e100801. PMC: 4069173. DOI: 10.1371/journal.pone.0100801. View

5.
Kang D, Nakagawa T, Feng L, Watanabe S, Han L, Mazzali M . A role for uric acid in the progression of renal disease. J Am Soc Nephrol. 2002; 13(12):2888-97. DOI: 10.1097/01.asn.0000034910.58454.fd. View