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Kidney Week

Abstract: TH-PO1047

Effects of Empagliflozin on Serum Uric Acid and Gout in CKD

Session Information

Category: CKD (Non-Dialysis)

  • 2302 CKD (Non-Dialysis): Clinical, Outcomes, and Trials

Author

  • Mayne, Kaitlin J., University of Oxford Nuffield Department of Population Health, Oxford, United Kingdom

Group or Team Name

  • The EMPA-KIDNEY Collaborative Group.
Background

Sodium-glucose co-transporter-2 (SGLT2) inhibitors reduce serum uric acid and may reduce the risk of gout in patients with diabetes and/or heart failure, but randomized evidence in patients with CKD is lacking.

Methods

EMPA-KIDNEY compared empagliflozin 10 mg daily with placebo in 6609 patients with CKD (Clinicaltrials.gov: NCT03594110). Eligible patients had an eGFR of 20 to <45; or 45 to <90 mL/min/1.73m2 with ≥200 mg/g albuminuria. Serum uric acid measured at randomization, 2 and 18 months was analyzed using a mixed model repeated measures approach including interaction terms to estimate subgroup-specific effects with calculation of heterogeneity or trend statistics. In exploratory analyses, first and total gout events were analyzed in Cox regression models with the Andersen-Gill extension for total events. All models were adjusted for age, sex, region, eGFR, uACR and diabetes status.

Results

Mean±SD baseline serum uric acid was 431.3±113.5 µmol/L. Empagliflozin reduced serum uric acid (study average between-group difference [95% CI] -25.6 [-30.3, -21.0] µmol/L). Uric acid lowering was greater in participants without diabetes (heterogeneity P<0.001) and at higher eGFR (trend P<0.001; Figure). During 2 years’ median follow-up, there was no significant effect of empagliflozin on risk of gout events alone (whether analyzing first or all occurrences, Table) which was consistent across subgroups including by baseline diabetes, eGFR and uric acid concentration (heterogeneity P all >0.1).

Conclusion

In EMPA-KIDNEY, empagliflozin modestly reduced serum uric acid with greater effects at higher eGFR and in those without diabetes, but did not significantly reduce episodes of gout.

Effects of empagliflozin versus placebo on gout
 Empagliflozin
n/N
Empagliflozin
Rate
per 1000
patient-years
Placebo
n/N
Placebo
Rate
per 1000
patient-years
Hazard Ratio
(95% CI)
First occurrence of gout278/330445.7317/330552.30.87 (0.74-1.02)
All occurrences of gout404/330462.2465/330571.70.86 (0.72-1.03)
First occurrence of gout or new initiation of xanthine oxidase inhibitor, primary uricosuric agent or colchicine in participants not on such therapy at randomization261/213566.3314/212481.80.81 (0.69-0.96)

Effects of empagliflozin versus placebo on serum uric acid and gout in subgroups defined by baseline characteristics

Funding

  • Commercial Support – EMPA-KIDNEY trial funding from Boehringer Ingelheim & Eli Lilly