Effects of Xanthine Oxidase Inhibition by Febuxostat on Lipid Profiles of Patients with Hyperuricemia: Insights from Randomized PRIZE Study.
Yuichi SaitoAtsushi TanakaHisako YoshidaHitoshi NakashimaNoriko BanMunehide MatsuhisaYoshio KobayashiKoichi Nodenull On Behalf Of The Prize Study InvestigatorsPublished in: Nutrients (2024)
Although patients with hyperuricemia and gout often have dyslipidemia, the effects of febuxostat, a xanthine oxidase inhibitor, on their lipid profiles are unclear. Thus, we performed a sub-analysis of the randomized PRIZE study in which the effects of febuxostat on carotid atherosclerosis were investigated in patients with hyperuricemia. The participants were randomized to the febuxostat or control group. The primary endpoint of this sub-analysis was changes in the patients' non-high-density lipoprotein cholesterol (HDL-C) levels from baseline to 6-month follow-up. Correlations between the changes in lipid profiles and cardiometabolic parameters were also evaluated. In total, 456 patients were included. From baseline to 6 months, non-HDL-C levels were significantly reduced in the febuxostat group (-5.9 mg/dL, 95% confidence interval [CI]: -9.1 to -2.8 mg/dL, p < 0.001), but not in the control group (-1.3 mg/dL, 95% CI: -4.4 to 1.8, p = 0.348). The reduction in non-HDL-C levels was more pronounced in women and correlated with changes in serum uric acid and estimated glomerular filtration rate levels only in the febuxostat group. In patients with hyperuricemia, febuxostat treatment was associated with reduced non-HDL-C levels from baseline to the 6-month follow-up compared to the control treatment, suggesting that the lipid-lowering effect of febuxostat should be considered when targeting dyslipidemia.
Keyphrases
- uric acid
- metabolic syndrome
- end stage renal disease
- double blind
- open label
- newly diagnosed
- ejection fraction
- chronic kidney disease
- phase iii
- prognostic factors
- phase ii
- peritoneal dialysis
- drug delivery
- mass spectrometry
- skeletal muscle
- adipose tissue
- insulin resistance
- combination therapy
- patient reported
- study protocol
- breast cancer risk