Kanbay Mehmet, Ozkara Adem, Selcoki Yusuf, Isik Bunyamin, Turgut Faruk, Bavbek Nuket, Uz Ebru, Akcay Ali, Yigitoglu Ramazan, Covic Adrian
35. Sokak, 81/5, Bahcelievler, Ankara, 06490, Turkey.
Int Urol Nephrol. 2007;39(4):1227-33. doi: 10.1007/s11255-007-9253-3. Epub 2007 Aug 15.
Hyperuricemia has been associated with the development of hypertension, cardiovascular, and renal disease. However, there is no data about the effect of lowering uric acid level on hypertension, renal function, and proteinuria in patients with glomerular filtration rate (GFR) >60 ml/min. We therefore conducted a prospective study to investigate the benefits of allopurinol treatment in hyperuricemic patients with normal renal function.
Forty-eight hyperuricemic and 21 normouricemic patients were included in the study. Hyperuricemic patients received 300 mg/day allopurinol for three months. All patients' serum creatinine level, 24-h urine protein level, glomerular filtration rate, and blood pressure levels were measured at baseline and after three months of treatment.
A total of 59 patients completed the three-month follow-up period of observation. In the allopurinol group, serum uric acid levels, GFR, systolic and diastolic blood pressure, and C-reactive protein (CRP) levels significantly improved (P < 0.05). However, urine protein excretion remained unchanged (P > 0.05). No correlation was observed between changes in GFR and changes in CRP, or blood pressure in the allopurinol group. No significant changes were observed in the control group (P > 0.05).
We bring indirect evidence that hyperuricemia increases blood pressure, and decreases GFR. Hence, management of hyperuricemia may prevent the progression of renal disease, even in patients with normal renal function, suggesting that early treatment with allopurinol should be an important part of the management of chronic kidney disease (CKD) patients. Long-term follow-up studies are warranted to identify the benefits of uric acid management on renal function and hypertension.
高尿酸血症与高血压、心血管疾病及肾脏疾病的发生相关。然而,对于肾小球滤过率(GFR)>60 ml/min的患者,降低尿酸水平对高血压、肾功能及蛋白尿的影响尚无相关数据。因此,我们进行了一项前瞻性研究,以探讨别嘌醇治疗对肾功能正常的高尿酸血症患者的益处。
本研究纳入了48例高尿酸血症患者和21例尿酸正常的患者。高尿酸血症患者接受每日300 mg别嘌醇治疗,为期三个月。在基线及治疗三个月后,测量所有患者的血清肌酐水平、24小时尿蛋白水平、肾小球滤过率及血压水平。
共有59例患者完成了为期三个月的观察随访期。在别嘌醇组中,血清尿酸水平、GFR、收缩压和舒张压以及C反应蛋白(CRP)水平均显著改善(P<0.05)。然而,尿蛋白排泄量未发生变化(P>0.05)。在别嘌醇组中,未观察到GFR变化与CRP变化或血压变化之间存在相关性。对照组未观察到显著变化(P>0.05)。
我们提供了间接证据,表明高尿酸血症会升高血压并降低GFR。因此,即使在肾功能正常的患者中,管理高尿酸血症也可能预防肾脏疾病的进展,这表明别嘌醇早期治疗应成为慢性肾脏病(CKD)患者管理的重要组成部分。有必要进行长期随访研究,以确定尿酸管理对肾功能和高血压的益处。