Takir Mumtaz, Kostek Osman, Ozkok Abdullah, Elcioglu Omer Celal, Bakan Ali, Erek Aybala, Mutlu Hasan Huseyin, Telci Ozge, Semerci Aysun, Odabas Ali Riza, Afsar Baris, Smits Gerard, ALanaspa Miguel, Sharma Shailendra, Johnson Richard J, Kanbay Mehmet
From the *Department of Medicine, Division of Endocrinology, †Department of Medicine, ‡Department of Medicine, Division of Nephrology, and §Departments of Biochemistry and ¶Family Medicine, Istanbul Medeniyet University, Goztepe Training and Research Hospital, Istanbul; and ∥Department of Medicine, Division of Nephrology, Konya Numune State Hospital, Konya, Turkey; **Division of Renal Diseases and Hypertension, University of Colorado, Denver, CO; and ††Department of Medicine, Division of Nephrology, Koc University School of Medicine, Istanbul, Turkey.
J Investig Med. 2015 Dec;63(8):924-9. doi: 10.1097/JIM.0000000000000242.
Hyperuricemia is an independent predictor of impaired fasting glucose and type 2 diabetes, but whether it has a causal role in insulin resistance remains controversial. Here we tested the hypothesis that lowering uric acid in hyperuricemic nondiabetic subjects might improve insulin resistance.
Subjects with asymptomatic hyperuricemia (n = 73) were prospectively placed on allopurinol (n = 40) or control (n = 33) for 3 months. An additional control group consisted of 48 normouricemic subjects. Serum uric acid, fasting glucose, fasting insulin, HOMA-IR (homeostatic model assessment of insulin resistance), and high-sensitivity C-reactive protein were measured at baseline and at 3 months.
Allopurinol-treated subjects showed a reduction in serum uric acid in association with improvement in fasting blood glucose, fasting insulin, and HOMA-IR index, as well as a reduction in serum high-sensitivity C-reactive protein. The number of subjects with impaired fasting glucose significantly decreased in the allopurinol group at 3 months compared with baseline (n = 8 [20%] vs n = 30 [75%], 3 months vs baseline, P < 0.001). In the hyperuricemic control group, only glucose decreased significantly and, in the normouricemic control, no end point changed.
Allopurinol lowers uric acid and improves insulin resistance and systemic inflammation in asymptomatic hyperuricemia. Larger clinical trials are recommended to determine if lowering uric acid can help prevent type 2 diabetes.
高尿酸血症是空腹血糖受损和2型糖尿病的独立预测因素,但它在胰岛素抵抗中是否具有因果作用仍存在争议。在此,我们检验了降低高尿酸血症非糖尿病患者尿酸水平可能改善胰岛素抵抗这一假设。
将无症状高尿酸血症患者(n = 73)前瞻性地分为别嘌醇组(n = 40)或对照组(n = 33),为期3个月。另一个对照组由48名尿酸正常的受试者组成。在基线和3个月时测量血清尿酸、空腹血糖、空腹胰岛素、HOMA-IR(胰岛素抵抗稳态模型评估)和高敏C反应蛋白。
别嘌醇治疗的受试者血清尿酸降低,同时空腹血糖、空腹胰岛素和HOMA-IR指数改善,血清高敏C反应蛋白也降低。与基线相比,别嘌醇组3个月时空腹血糖受损的受试者数量显著减少(3个月时n = 8 [20%],基线时n = 30 [75%],P < 0.001)。在高尿酸血症对照组中,只有血糖显著降低;而在尿酸正常对照组中,无终点指标发生变化。
别嘌醇可降低无症状高尿酸血症患者的尿酸水平,改善胰岛素抵抗和全身炎症。建议开展更大规模的临床试验,以确定降低尿酸是否有助于预防2型糖尿病。