An-Ping Huo, Shiow-Ing Wang, Pui-Ying Leong, James Cheng-Chung Wei, Tsai-Ching Hsu
In individuals without major cardiometabolic disease, initiating ULT was associated with increased cardiometabolic risk. Serum urate may have context-dependent physiological roles in early metabolic states, warranting further research.
BACKGROUND: Whether urate-lowering therapy (ULT) affects cardiometabolic outcomes in individuals without established metabolic disease remains uncertain.
MATERIALS AND METHODS: This retrospective cohort study used TriNetX data (2015-2023) to include adults with newly diagnosed hyperuricemia (UA >7 mg/dL) and no baseline diabetes, cardiovascular disease, or metabolic disorders. Patients initiating ULT were propensity score-matched (1:1) to untreated controls (2,906 pairs). The primary outcome was a composite cardiometabolic endpoint.
RESULTS: Over a median follow-up of 3.03 years, ULT initiation was associated with increased risk of the composite cardiometabolic outcome (HR 1.18, 95% CI 1.07-1.30) and of all-cause mortality (HR 1.52, 95% CI 1.27-1.82). The increased risk was evident among men, individuals without prior gout, users of xanthine oxidase inhibitors, and those who achieved target serum urate (<5 mg/dL) within 6 months.
CONCLUSIONS: In individuals without major cardiometabolic disease, initiating ULT was associated with increased cardiometabolic risk. Serum urate may have context-dependent physiological roles in early metabolic states, warranting further research.