尿毒清颗粒联合非布司他治疗高尿酸血症肾损害临床研究
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R589.7

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2023年浙江省医学会临床医学专项资金项目(2023ZYC-B26)


Clinical Study on Treatment of Renal Damage Due to Hyperuricemia with Niaoduqing Granules Combined with Febuxostat
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    摘要:

    目的:观察尿毒清颗粒联合非布司他治疗高尿酸血症肾损害患者的疗效。方法:选取2022年7月— 2024年7月诸暨市第六人民医院收治的160例高尿酸血症肾损害患者,按随机数字表法分为研究组及对照组各 80例。研究组给予尿毒清颗粒联合非布司他治疗,对照组给予非布司他治疗。比较2组临床疗效及不良反应发 生率,比较2组治疗前后肾功能指标值[尿酸(UA)、肌酐(SCr)、血清胱抑素C(Cys C)]、血管内皮功能 [血清内皮素-1(ET-1)、一氧化氮(NO)]、炎性因子[超敏C-反应蛋白(hs-CRP)、白细胞介素-6(IL-6)、 肿瘤坏死因子-α (TNF-α)] 水平的变化。结果:研究组临床疗效总有效率为91.25% (73/80),对照组为 77.50% (62/80),2 组临床疗效比较,差异有统计学意义(P<0.05)。治疗2个月后,2组Cys C、SCr、UA水 平均较治疗前下降(P<0.05),研究组上述3项水平均低于对照组(P<0.05)。治疗2个月后,2组ET-1水平 均较治疗前下降(P<0.05),NO水平均较治疗前上升(P<0.05);研究组ET-1水平低于对照组(P<0.05), NO 水平高于对照组(P<0.05)。治疗2 个月后,2 组hs-CRP、IL-6、TNF-α 水平均较治疗前下降(P< 0.05),研究组上述3 项水平均低于对照组(P<0.05)。对照组不良反应发生率为10.00% (8/80),研究组 不良反应发生率为6.25%(5/80),2组不良反应发生率比较,差异无统计学意义(P>0.05)。结论:尿毒清颗粒 联合非布司他能提升高尿酸血症肾损害患者的临床疗效,改善肾功能及血管内皮功能,减轻炎症反应,安全性高。

    Abstract:

    Abstract: Objective: To observe the therapeutic effects of Niaoduqing Granules combined with Febuxostat in patients with renal damage due to hyperuricemia. Methods: A total of 160 patients with renal damage due to hyperuricemia treated at Zhuji Sixth People's Hospital from July 2022 to July 2024 were selected and divided into a study group and a control group,with 80 cases in each group,using a random number table method. The study group was treated with Niaoduqing Granules combined with Febuxostat,while the control group was treated with Febuxostat alone. Clinical effects and the incidence of adverse reactions were compared between the two groups. Renal function indicators [uric acid (UA),serum creatinine (SCr),and serum cystatin C (Cys C)],vascular endothelial function [serum endothelin-1 (ET-1) and nitric oxide (NO)], and inflammatory factors [high-sensitivity C-reactive protein (hs-CRP),interleukin-6 (IL-6),and tumor necrosis factor-α (TNF-α)] levels were compared before and after treatment. Results:The total effective rate of clinical efficacy in the study group was 91.25%(73/80),compared to 77.50%(62/80) in the control group, with difference being significant (P<0.05). After two months of treatment, Cys C,SCr,and UA levels in both groups were decreased compared to those before treatment (P<0.05),with the study group achieving lower levels than the control group (P<0.05). After two months of treatment,ET-1 levels in both groups were decreased (P<0.05),while NO levels were increased (P<0.05). The study group had lower ET-1 levels and higher NO levels than the control group (P<0.05). After two months of treatment,hs-CRP,IL-6,and TNF-α levels in both groups were decreased compared to those before treatment (P<0.05), with the study group achieving lower levels than the control group (P<0.05). The incidence of adverse reactions was 10.00%(8/80) in the control group and 6.25%(5/80) in the study group, with no significant difference between the two groups (P>0.05). Conclusion: The combination of Niaoduqing Granules and Febuxostat can improve clinical efficacy in patients with renal damage due to hyperuricemia, enhance renal function and vascular endothelial function, and reduce inflammatory responses,with high safety.

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赵俞,姚丹萍,赵鑫海.尿毒清颗粒联合非布司他治疗高尿酸血症肾损害临床研究[J].新中医,2025,57(13):67-71

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  • 在线发布日期: 2025-07-14
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