Type 2 & other diabetes

Effects of ertugliflozin on uric acid and gout‐related outcomes in persons with type 2 diabetes and cardiovascular disease: Post hoc analyses from VERTIS CV

Diabetes Obes MetabPublished Post hoc analysis of the VERTIS CV randomised trial

Primary result · LSM change from baseline in UAResult — go to the resultPlacebo-adjusted LSM change −0.26 mg/dL 95% CI −0.36 to −0.16

Authors' conclusion

Ertugliflozin was generally associated with lowering UA overall and across subgroups compared with placebo, and numerically reduced rates of gout-related outcome events.

Study context

Population
Participants with T2D and atherosclerotic CVD
Comparison
Pooled ertugliflozin vs placebo
Primary endpoint
Mean serum uric acid (UA) over time
Follow-up
260 weeks

Primary result

LSM change from baseline in UA · Week 260

Placebo-adjusted least squares mean (LSM) change

−0.26 mg/dL

95% CI −0.36 to −0.16

Change by group

Placebo

0.07

LSM change · 95% CI −0.02–0.15 · mg/dL

Ertugliflozin

−0.19

LSM change · 95% CI −0.25–-0.13 · mg/dL

Ertugliflozinvs Placebo
placebo-adjusted LSM change −0.26 mg/dL (95% CI −0.36 to −0.16)

As reported in the abstract

Further findings

Baseline mean UA

OutcomeErtugliflozinPlaceboHR (95% CI)
Composite of gout onset or initiation of anti-gout medication2.6%3.3%0.76 (0.580–1.002)

Uric acid (UA) by baseline UA quintile

Ertugliflozin associated with reductions in UA across baseline UA quintiles vs placebo

Original publication

Effects of ertugliflozin on uric acid and gout‐related outcomes in persons with type 2 diabetes and cardiovascular disease: Post hoc analyses from VERTIS CV. Diabetes Obes Metab. Published 2 September 2024. doi:10.1111/dom.15895

Composed by AI from the published abstract and checked against it. How Briefs are made →

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