Department of Medicine, Division of Nephrology, Toronto General Hospital, University of Toronto, Toronto, Ontario, Canada.
Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada.
Diabetes. 2017 Jul;66(7):1939-1949. doi: 10.2337/db17-0168. Epub 2017 Apr 13.
Higher plasma uric acid (PUA) levels are associated with lower glomerular filtration rate (GFR) and higher blood pressure (BP) in patients with type 1 diabetes (T1D). Our aim was to determine the impact of PUA lowering on renal and vascular function in patients with uncomplicated T1D. T1D patients ( = 49) were studied under euglycemic and hyperglycemic conditions at baseline and after PUA lowering with febuxostat (FBX) for 8 weeks. Healthy control subjects were studied under normoglycemic conditions ( = 24). PUA, GFR (inulin), effective renal plasma flow (para-aminohippurate), BP, and hemodynamic responses to an infusion of angiotensin II (assessment of intrarenal renin-angiotensin-aldosterone system [RAAS]) were measured before and after FBX treatment. Arterial stiffness, flow-mediated dilation (FMD), nitroglycerin-mediated dilation (GMD), urinary nitric oxide (NO), and inflammatory markers were measured before and after FBX treatment. Gomez equations were used to estimate arteriolar afferent resistance, efferent resistance (R), and glomerular hydrostatic pressure (P). FBX had a modest systolic BP-lowering effect in T1D patients (112 ± 10 to 109 ± 9 mmHg, = 0.049) without impacting arterial stiffness, FMD, GMD, or NO. FBX enhanced the filtration fraction response to hyperglycemia in T1D patients through larger increases in R P, and interleukin-18 but without impacting the RAAS. FBX lowered systolic BP and modulated the renal R responses to hyperglycemia but without impacting the RAAS or NO levels, suggesting that PUA may augment other hemodynamic or inflammatory mechanisms that control the renal response to hyperglycemia at the efferent arteriole. Ongoing outcome trials will determine cardiorenal outcomes of PUA lowering in patients with T1D.
高尿酸血症(PUA)水平与 1 型糖尿病(T1D)患者的肾小球滤过率(GFR)降低和血压(BP)升高有关。我们的目的是确定降低 PUA 对无并发症 T1D 患者的肾脏和血管功能的影响。T1D 患者(n = 49)在基线时和使用非布司他(FBX)降低 PUA 8 周后进行了血糖正常和高血糖条件下的研究。健康对照受试者(n = 24)在血糖正常条件下进行了研究。在 FBX 治疗前后测量了 PUA、GFR(菊粉)、有效肾血浆流量(对氨基马尿酸)、BP 和血管紧张素 II 输注的血液动力学反应(评估肾内肾素-血管紧张素-醛固酮系统[RAAS])。在 FBX 治疗前后测量了动脉僵硬度、血流介导的扩张(FMD)、硝酸甘油介导的扩张(GMD)、尿一氧化氮(NO)和炎症标志物。使用 Gomez 方程估计小动脉传入阻力、传出阻力(R)和肾小球静水压力(P)。FBX 在 T1D 患者中具有适度的收缩压降低作用(从 112 ± 10 至 109 ± 9 mmHg,P = 0.049),但不影响动脉僵硬度、FMD、GMD 或 NO。FBX 通过更大程度地增加 R P 和白细胞介素-18 增强了 T1D 患者高血糖时的滤过分数反应,但不影响 RAAS。FBX 降低了收缩压并调节了肾脏对高血糖的 R 反应,但不影响 RAAS 或 NO 水平,这表明 PUA 可能增强了控制高血糖时肾脏对高血糖反应的其他血液动力学或炎症机制。正在进行的结局试验将确定降低 T1D 患者 PUA 的心脏肾脏结局。