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. 2020 Feb 4;172(3):186-194.
doi: 10.7326/M19-2610. Epub 2020 Jan 14.

Assessing the Risk for Gout With Sodium-Glucose Cotransporter-2 Inhibitors in Patients With Type 2 Diabetes: A Population-Based Cohort Study

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Assessing the Risk for Gout With Sodium-Glucose Cotransporter-2 Inhibitors in Patients With Type 2 Diabetes: A Population-Based Cohort Study

Michael Fralick et al. Ann Intern Med. .

Abstract

Background: Hyperuricemia is common in patients with type 2 diabetes mellitus and is known to cause gout. Sodium-glucose cotransporter-2 (SGLT2) inhibitors prevent glucose reabsorption and lower serum uric acid levels.

Objective: To compare the rate of gout between adults prescribed an SGLT2 inhibitor and those prescribed a glucagon-like peptide-1 (GLP1) receptor agonist.

Design: Population-based new-user cohort study.

Setting: A U.S. nationwide commercial insurance database from March 2013 to December 2017.

Patients: Persons with type 2 diabetes newly prescribed an SGLT2 inhibitor were 1:1 propensity score matched to patients newly prescribed a GLP1 agonist. Persons were excluded if they had a history of gout or had received gout-specific treatment previously.

Measurements: The primary outcome was a new diagnosis of gout. Cox proportional hazards regression was used to estimate hazard ratios (HRs) of the primary outcome and 95% CIs.

Results: The study identified 295 907 adults with type 2 diabetes mellitus who were newly prescribed an SGLT2 inhibitor or a GLP1 agonist. The gout incidence rate was lower among patients prescribed an SGLT2 inhibitor (4.9 events per 1000 person-years) than those prescribed a GLP1 agonist (7.8 events per 1000 person-years), with an HR of 0.64 (95% CI, 0.57 to 0.72) and a rate difference of -2.9 (CI, -3.6 to -2.1) per 1000 person-years.

Limitation: Unmeasured confounding, missing data (namely incomplete laboratory data), and low baseline risk for gout.

Conclusion: Adults with type 2 diabetes prescribed an SGLT2 inhibitor had a lower rate of gout than those prescribed a GLP1 agonist. Sodium-glucose cotransporter-2 inhibitors may reduce the risk for gout among adults with type 2 diabetes mellitus, although future studies are necessary to confirm this observation.

Primary funding source: Brigham and Women's Hospital.

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Figures

Figure 1.
Figure 1.
Cohort entry. GLP1 = glucagon-like peptide 1, SGLT2 = sodium-glucose cotransporter 2 HIV = human immunodeficiency virus, AIDS = acquired immune deficiency syndrome. Gout medications included: allopurinol, febuxostat, pegloticase, probenecid, colchicine
Figure 2.
Figure 2.
Kaplan–Meier curve for propensity score–matched rate of gout. GLP1 = glucagon-like peptide-1 agonist, SGLT2 = sodium–glucose cotransporter-2 inhibitor.

References

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