Liu Shuang, Liu Qingsong, Gu Ronger, Wu Mian, Meng Shuo, Yan Le, Chen Qi, Zhu Cuiling, Chen Si, Xu Bei, Liu Fengjing, Chen Haibing
Department of Endocrinology and Metabolism, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, People's Republic of China.
Department of Pharmacy, Heze Municipal hospital, Heze, People's Republic of China.
Drug Des Devel Ther. 2025 Jun 5;19:4875-4884. doi: 10.2147/DDDT.S522154. eCollection 2025.
Hyperuricemia (HUA) has been linked to an elevated risk of impaired glucose metabolism. This study aimed to investigated the impact of the urate-lowering drug febuxostat on blood glucose levels, insulin sensitivity, and β-cell function in subjects with HUA who present with normoglycemia, prediabetes, or newly diagnosed type 2 diabetes (T2DM).
We assessed the glucose metabolism of participants with HUA using a 3-h oral glucose tolerance test (OGTT). Participants were categorized into two groups: those with HUA and normal glucose metabolism (NGM, n=28), and those with HUA and abnormal glucose metabolism (AbGM, n=32), including prediabetes (n=20) and newly diagnosed T2DM (n=12). Both groups received a daily dose of 40 mg febuxostat for 24 consecutive weeks and underwent 3-h OGTT at 12 and 24 weeks. Glucose, insulin, and C-peptide were measured to calculate insulin sensitivity (Stumvoll index, Gutt index) and β-cell function (Insulin Secretion-Sensitivity Index-2 and Disposition Index) indices. Differences in glucose levels and indices were analyzed by repeated measures ANOVA including interaction terms between groups and the time of visit.
After 24 weeks of febuxostat treatment, subjects with HUA and AbGM showed significant reductions in postprandial 1-h (11.88±1.39mmol/L at baseline, 10.97±2.74mmol/L at 12 weeks, and 11.12±1.92mmol/L at 24 weeks, Ptime=0.031) and 2-h glucose (10.25±1.71mmol/L at baseline, 9.39±2.77mmol/L at 12 weeks, and 9.16±2.67mmol/L at 24 weeks, Ptime=0.014). Febuxostat significantly improved insulin sensitivity of subjects in the AbGM group, but did not affect β-cell function. Moreover, the improvement in insulin sensitivity in these subjects was not directly correlated with the improvement in uric acid. No significant changes were observed in subjects with NGM.
In subjects with HUA and prediabetes or newly diagnosed T2DM, febuxostat significantly enhanced postprandial glucose and insulin sensitivity, though it did not notably improve β-cell function. Further research is required to explore how febuxostat enhances insulin sensitivity.
高尿酸血症(HUA)与糖代谢受损风险升高有关。本研究旨在调查降尿酸药物非布司他对血糖正常、糖尿病前期或新诊断的2型糖尿病(T2DM)的高尿酸血症患者血糖水平、胰岛素敏感性和β细胞功能的影响。
我们采用3小时口服葡萄糖耐量试验(OGTT)评估高尿酸血症参与者的糖代谢情况。参与者分为两组:高尿酸血症且糖代谢正常(NGM,n = 28)组和高尿酸血症且糖代谢异常(AbGM,n = 32)组,后者包括糖尿病前期(n = 20)和新诊断的T2DM(n = 12)患者。两组均连续24周每日服用40 mg非布司他,并在第12周和第24周进行3小时OGTT。测量血糖、胰岛素和C肽以计算胰岛素敏感性(Stumvoll指数、Gutt指数)和β细胞功能(胰岛素分泌-敏感性指数-2和处置指数)指标。采用重复测量方差分析,包括组间和就诊时间的交互项,分析血糖水平和指标的差异。
非布司他治疗24周后,高尿酸血症且糖代谢异常的患者餐后1小时血糖(基线时为11.88±1.39mmol/L,12周时为10.97±2.74mmol/L,24周时为11.12±1.92mmol/L,P时间=0.031)和餐后2小时血糖(基线时为10.25±1.71mmol/L,12周时为9.39±2.77mmol/L,24周时为9.16±2.67mmol/L,P时间=0.014)显著降低。非布司他显著改善了糖代谢异常组患者的胰岛素敏感性,但对β细胞功能无影响。此外,这些患者胰岛素敏感性的改善与尿酸的改善无直接相关性。糖代谢正常组患者未观察到显著变化。
在高尿酸血症合并糖尿病前期或新诊断T2DM的患者中,非布司他显著提高了餐后血糖和胰岛素敏感性,尽管它并未显著改善β细胞功能。需要进一步研究以探索非布司他如何提高胰岛素敏感性。