Tsuji Takayuki, Ohishi Kazuhisa, Takeda Asumi, Goto Daiki, Sato Taichi, Ohashi Naro, Fujigaki Yoshihide, Kato Akihiko, Yasuda Hideo
Internal Medicine 1, Division of Nephrology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka, 431-3192, Japan.
Department of Nephrology, Hamamatsu Medical Center, Hamamatsu, Shizuoka, Japan.
Clin Exp Nephrol. 2018 Dec;22(6):1300-1308. doi: 10.1007/s10157-018-1580-4. Epub 2018 Apr 26.
Febuxostat is tolerable in chronic kidney disease (CKD) patients with hyperuricemia. However, the long-term effect of lowering uric acid with febuxostat on renal function and blood pressure has not been elucidated.
This was a 2 years retrospective observational study. 86 CKD patients with hyperuricemia who continued with allopurinol (allopurinol group, n = 30), switched from allopurinol to febuxostat (switched group, n = 25), or were newly prescribed febuxostat (febuxostat group, n = 31) were included in this study. Serum uric acid, estimated glomerular filtration rate (eGFR), blood pressure, and urinary protein were analyzed. Moreover, the impact of serum uric acid reduction on renal function and blood pressure was assessed.
Serum uric acid in the switched and febuxostat groups was significantly reduced at 6 months (switched group; 8.49 ± 1.32-7.19 ± 1.14 mg/dL, p < 0.0001, febuxostat group; 9.43 ± 1.63-6.31 ± 0.90 mg/dL, p < 0.0001). In the allopurinol group, serum uric acid was increased (6.86 ± 0.87-7.10 ± 0.85 mg/dL, p = 0.0213). eGFR was significantly increased (35.2 ± 12.8-37.3 ± 13.9 mL/min/1.73 m, p = 0.0232), while mean arterial pressure (93.1 ± 10.8-88.2 ± 9.5 mmHg, p = 0.0039) was significantly decreased at 6 months in the febuxostat group, resulting in the retention of eGFR for 2 years.
The impact of serum uric acid reduction might have beneficial effects on CKD progression and blood pressure. However, a large prospective study is needed to determine the long-term efficacy of febuxostat therapy in CKD patients with hyperuricemia.
非布司他对于慢性肾脏病(CKD)合并高尿酸血症患者而言耐受性良好。然而,非布司他降尿酸治疗对肾功能和血压的长期影响尚未阐明。
这是一项为期2年的回顾性观察研究。本研究纳入了86例CKD合并高尿酸血症患者,其中继续使用别嘌醇的患者(别嘌醇组,n = 30)、从别嘌醇换用非布司他的患者(换药组,n = 25)或新使用非布司他的患者(非布司他组,n = 31)。分析了血清尿酸、估算肾小球滤过率(eGFR)、血压和尿蛋白。此外,评估了血清尿酸降低对肾功能和血压的影响。
换药组和非布司他组在6个月时血清尿酸显著降低(换药组:8.49±1.32 - 7.19±1.14mg/dL,p < 0.0001;非布司他组:9.43±1.63 - 6.31±0.90mg/dL,p < 0.0001)。别嘌醇组血清尿酸升高(6.86±0.87 - 7.10±0.85mg/dL,p = 0.0213)。非布司他组在6个月时eGFR显著升高(35.2±12.8 - 37.3±13.9mL/min/1.73m²,p = 0.0232),而平均动脉压显著降低(93.1±10.8 - 88.2±9.5mmHg,p = 0.0039),eGFR维持2年。
血清尿酸降低可能对CKD进展和血压具有有益影响。然而,需要开展大型前瞻性研究以确定非布司他治疗CKD合并高尿酸血症患者的长期疗效。