非布司他治疗2型糖尿病肾病合并高尿酸血症的临床观察
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篇名: 非布司他治疗2型糖尿病肾病合并高尿酸血症的临床观察
TITLE:
摘要: 目的:观察非布司他治疗2型糖尿病肾病(DN)合并高尿酸血症的临床疗效及安全性。方法:选择2014年1月-2016年6月我院收治的2型DN合并高尿酸血症患者137例,按随机数字表法分为A组(46例)、B组(47例)、C组(44例)。在常规治疗方案的基础上,A组患者口服别嘌醇片,起始剂量0.05 g,bid;2周后增至0.10 g,bid。B组患者口服苯溴马隆片50 mg,qd。C组患者口服非布司他片,起始剂量40 mg,qd;2周后增至80 mg,qd。所有患者均连续治疗12周。观察两组患者的临床疗效以及治疗前后血尿酸(SUA)、血肌酐(Scr)、血尿素氮(BUN)水平,并记录不良反应发生情况。结果:A、B、C组各有4、6、3例患者脱落。B、C组患者的总有效率(87.8%、85.4%)显著高于A组(76.2%),差异均有统计学意义(P<0.05);而B、C组比较差异无统计学意义(P>0.05)。治疗前,3组患者SUA、Scr、BUN水平比较,差异均无统计学意义(P>0.05)。治疗后4周,3组患者SUA水平均较治疗前显著降低,差异均有统计学意义(P<0.05);但其余指标组间及治疗前后比较,差异均无统计学意义(P>0.05)。治疗后12周,3组患者SUA水平均较治疗前和治疗后4周显著降低,且B、C组显著低于A组;A、C组患者Scr水平均较治疗前显著降低,B组较治疗前显著升高,且B组显著高于A、C组,差异均有统计学意义(P<0.05);但3组患者Scr、BUN水平与治疗后4周比较,B、C组SUA水平比较,A、C组Scr水平比较,差异均无统计学意义(P>0.05)。C组患者的不良反应总发生率(12.20%)显著低于A、B组(25.58%、24.39%),差异均有统计学意义(P<0.05);而A、B组比较差异无统计学意义(P>0.05)。结论:非布司他降低2型DN合并高尿酸血症患者SUA水平的效果优于别嘌醇,且对肾功能的影响小,安全性更高。
ABSTRACT: OBJECTIVE: To observe clinical efficacy and safety of febuxostat in the treatment of type 2 diabetic nephropathy complicated with hyperuricemia. METHODS: A total of 137 patients with type 2 diabetic nephropathy complicated with hyperuricemia selected from our hospital during Jan. 2014-Jun. 2016 were divided into group A (46 cases), B (47 cases), C (44 cases) according to random number table. On the basis of routine treatment, group A was given Allopurinol tablets orally with initial dose of 0.05 g, bid; increasing to 0.10 g, bid, 2 weeks later. Group B was given Benzbromarone tablets 50 mg orally, qd. Group C was given Febuxostat tablets orally with initial dose of 40 mg, qd; increasing to 80 mg, qd, 2 weeks later. All patients received treatment for consecutive 12 weeks. Clinical efficacies of 2 groups were observed, and the levels of serum uric acid (SUA), Scr and BUN were also observed before and after treatment. The occurrence of ADR was recorded. RESULTS: Four, six, three patients withdrew from the study in group A, B, C, respectively. The total response rates of group B, C (87.8%, 85.4%) were significantly higher than that of group A (76.2%), with statistical significance (P<0.05); there was no statistical significance between group B and C (P>0.05). Before treatment, there was no statistical significance in the levels of SUA, Scr or BUN among 3 groups (P>0.05). Four weeks after treatment, the levels of SUA in 3 groups were decreased significantly compared to before treatment, with statistical significance (P<0.05); there was no statistical significance in other indexes among 3 groups or between before and after treatment (P>0.05). Twelve weeks after treatment, the levels of SUA in 3 groups were decreased significantly compared to before treatment and 4 weeks after treatment, and group B and C were significantly lower than group A; the levels of Scr in group A and C were decreased significantly compared to before treatment, while that of group B was increased significantly compared to before treatment and group B was significantly higher than group A and C, with statistical significance (P<0.05). There was no statistical significance in the levels of Scr or BUN among 3 groups compared to 4 weeks after treatment; there was also no statistical significance in the levels of SUA between group B and C, the levels of Scr between group A and C (P>0.05). Total incidence of ADR in group C (12.20%) was significantly lower than group A and B (25.58%, 24.39%), with statistical significance (P<0.05); there was no statistical significance between group A and B (P>0.05). CONCLUSIONS: Febuxostat is better than allopurinol in reducing the level of SUA in type 2 diabetic nephropathy patients with hyperuricemia. It shows small effect on renal function with better safety.
期刊: 2018年第29卷第4期
作者: 张春林,王小翠,王慧,童强,张瑞
AUTHORS: ZHANG Chunlin,WANG Xiaocui,WANG Hui,TONG Qiang,ZHANG Rui
关键字: 非布司他;别嘌醇;苯溴马隆;2型糖尿病肾病;高尿酸血症;临床疗效;血尿酸;血肌酐;血尿素氮
KEYWORDS: Febuxostat; Allopurinol; Benzbromarone; Type 2 diabetic nephropathy; Hyperuricemia; Clinical efficacy; Serum uric acid; Scr; BUN
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