TY - JOUR
T1 - Effect of Intensive Urate Lowering With Combined Verinurad and Febuxostat on Albuminuria in Patients With Type 2 Diabetes
T2 - A Randomized Trial
AU - Stack, Austin G.
AU - Dronamraju, Nalina
AU - Parkinson, Joanna
AU - Johansson, Susanne
AU - Johnsson, Eva
AU - Erlandsson, Fredrik
AU - Terkeltaub, Robert
N1 - Publisher Copyright:
© 2020 The Authors
PY - 2021/4
Y1 - 2021/4
N2 - Rationale & Objective: Hyperuricemia has been implicated in the development and progression of chronic kidney disease. Verinurad is a novel, potent, specific urate reabsorption inhibitor. We evaluated the effects on albuminuria of intensive urate-lowering therapy with verinurad combined with the xanthine oxidase inhibitor febuxostat in patients with hyperuricemia and type 2 diabetes mellitus (T2DM). Study Design: Phase 2, multicenter, prospective, randomized, double-blind, parallel-group, placebo-controlled trial. Setting & Participants: Patients 18 years or older with hyperuricemia, albuminuria, and T2DM. Intervention: Patients randomly assigned 1:1 to verinurad (9 mg) plus febuxostat (80 mg) or matched placebo once daily for 24 weeks. Outcomes: The primary end point was change in urinary albumin-creatinine ratio (UACR) from baseline after 12 weeks’ treatment. Secondary end points included safety and tolerability and effect on glomerular filtration. Results: 60 patients were enrolled (n = 32, verinurad and febuxostat; n = 28, placebo). UACRs after treatment with verinurad plus febuxostat were lower than after placebo at 1, 12, and 24 weeks: −38.6% (90% CI, −60.9% to −3.6%), −39.4% (90% CI, −61.8% to −3.8%), and −49.3% (90% CI, −68.2% to −19.0%), respectively. Serum urate levels after treatment with verinurad plus febuxostat were 59.6% and 63.7% lower than after placebo at 12 and 24 weeks, respectively. No clinically meaningful changes were observed in estimated glomerular filtration rate or serum creatinine or serum cystatin C concentrations. Verinurad plus febuxostat was well tolerated. Limitations: Sample size and study duration were insufficient to evaluate definitive effects of verinurad plus febuxostat on UACR and glomerular filtration. Generalizability was limited by exclusion of patients with stages 4 and 5 chronic kidney disease. Conclusions: Verinurad plus febuxostat reduced albuminuria and lowered serum urate concentrations in patients with T2DM, albuminuria, and hyperuricemia. Definitive assessment of their combined impact on preservation of kidney function awaits larger clinical studies. Funding: This study was supported by AstraZeneca. Trial Registration: Registered at ClinicalTrials.gov with study number NCT03118739.
AB - Rationale & Objective: Hyperuricemia has been implicated in the development and progression of chronic kidney disease. Verinurad is a novel, potent, specific urate reabsorption inhibitor. We evaluated the effects on albuminuria of intensive urate-lowering therapy with verinurad combined with the xanthine oxidase inhibitor febuxostat in patients with hyperuricemia and type 2 diabetes mellitus (T2DM). Study Design: Phase 2, multicenter, prospective, randomized, double-blind, parallel-group, placebo-controlled trial. Setting & Participants: Patients 18 years or older with hyperuricemia, albuminuria, and T2DM. Intervention: Patients randomly assigned 1:1 to verinurad (9 mg) plus febuxostat (80 mg) or matched placebo once daily for 24 weeks. Outcomes: The primary end point was change in urinary albumin-creatinine ratio (UACR) from baseline after 12 weeks’ treatment. Secondary end points included safety and tolerability and effect on glomerular filtration. Results: 60 patients were enrolled (n = 32, verinurad and febuxostat; n = 28, placebo). UACRs after treatment with verinurad plus febuxostat were lower than after placebo at 1, 12, and 24 weeks: −38.6% (90% CI, −60.9% to −3.6%), −39.4% (90% CI, −61.8% to −3.8%), and −49.3% (90% CI, −68.2% to −19.0%), respectively. Serum urate levels after treatment with verinurad plus febuxostat were 59.6% and 63.7% lower than after placebo at 12 and 24 weeks, respectively. No clinically meaningful changes were observed in estimated glomerular filtration rate or serum creatinine or serum cystatin C concentrations. Verinurad plus febuxostat was well tolerated. Limitations: Sample size and study duration were insufficient to evaluate definitive effects of verinurad plus febuxostat on UACR and glomerular filtration. Generalizability was limited by exclusion of patients with stages 4 and 5 chronic kidney disease. Conclusions: Verinurad plus febuxostat reduced albuminuria and lowered serum urate concentrations in patients with T2DM, albuminuria, and hyperuricemia. Definitive assessment of their combined impact on preservation of kidney function awaits larger clinical studies. Funding: This study was supported by AstraZeneca. Trial Registration: Registered at ClinicalTrials.gov with study number NCT03118739.
KW - Albuminuria
KW - cardiovascular outcomes
KW - chronic kidney disease (CKD)
KW - febuxostat
KW - hyperuricemia
KW - randomized controlled trial (RCT)
KW - renal function
KW - safety
KW - type 2 diabetes
KW - urate lowering
KW - urinary albumin-creatinine ratio (UACR)
KW - verinurad
UR - http://www.scopus.com/inward/record.url?scp=85099106452&partnerID=8YFLogxK
U2 - 10.1053/j.ajkd.2020.09.009
DO - 10.1053/j.ajkd.2020.09.009
M3 - Article
C2 - 33130235
AN - SCOPUS:85099106452
SN - 0272-6386
VL - 77
SP - 481
EP - 489
JO - American Journal of Kidney Diseases
JF - American Journal of Kidney Diseases
IS - 4
ER -