首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >Efficacy and safety of Abelmoschus manihot for primary glomerular disease: A prospective, multicenter randomized controlled clinical trial
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Efficacy and safety of Abelmoschus manihot for primary glomerular disease: A prospective, multicenter randomized controlled clinical trial

机译:黄芪对原发性肾小球疾病的疗效和安全性:一项前瞻性,多中心,随机对照临床试验

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Background Abelmoschus manihot, a single medicament of traditional Chinese medicine, has been widely used to treat kidney disease. This is the first randomized controlled clinical trial to assess its efficacy and safety in patients with primary glomerular disease. Study Design Prospective, open-label, multicenter, randomized, controlled, clinical trial. Setting & Participants From May 2010 to October 2011, a total of 417 patients with biopsy-proven primary glomerular disease from 26 hospitals participated in the study. Interventions A manihot in the form of a huangkui capsule, 2.5 g, 3 times per day; losartan potassium, 50 mg/d; or combined treatment, a huangkui capsule at 2.5 g 3 times per day, was combined with losartan potassium, 50 mg/d. The duration of intervention was 24 weeks. Outcomes & Measurements The primary outcome was change in 24-hour proteinuria from baseline after treatment. Change in estimated glomerular filtration rate (eGFR) from baseline after treatment was a secondary outcome. The 24-hour proteinuria was measured every 4 weeks and eGFR was measured at 0, 4, 12, and 24 weeks. Results Mean baseline urine protein excretion was 1,045, 1,084, and 1,073 mg/d in the A manihot, losartan, and combined groups, respectively, and mean eGFR was 108, 106, and 106 mL/min/1.73 m2, respectively. After 24 weeks of treatment, mean changes in proteinuria were protein excretion of -508, -376, and -545 mg/d, respectively (P = 0.003 for A manihot vs losartan and P 0.001 for the combined treatment vs losartan). Mean eGFR did not change significantly. The incidence of adverse reactions was not different among the 3 groups (P 0.05), and there were no severe adverse events in any group. Limitations Results cannot be generalized to those with nephrotic syndrome or reduced eGFR. Conclusions A manihot is a promising therapy for patients with primary kidney disease (chronic kidney disease stages 1-2) with moderate proteinuria.
机译:背景技术Abelmoschus manihot是一种传统中药,已被广泛用于治疗肾脏疾病。这是第一项评估其在原发性肾小球疾病患者中的疗效和安全性的随机对照临床试验。研究设计前瞻性,开放标签,多中心,随机,对照,临床试验。背景与参与者从2010年5月至2011年10月,来自26家医院的417例经活检证实为原发性肾小球疾病的患者参加了研究。干预措施:黄ku胶囊2.5克,每天3次。氯沙坦钾,50 mg / d;或联合治疗,将每日2.5 g的黄葵胶囊与50毫克/天的氯沙坦钾合用。干预时间为24周。结果与测量主要结果是治疗后基线时24小时蛋白尿发生变化。治疗后基线估计的肾小球滤过率(eGFR)的变化是次要结果。每4周测量24小时蛋白尿,在0、4、12和24周测量eGFR。结果A芒果,氯沙坦和联合治疗组的平均基线尿蛋白排泄量分别为1,045、1,084和1,073 mg / d,平均eGFR分别为108、106和106 mL / min / 1.73 m2。治疗24周后,蛋白尿的平均变化分别为-508,-376和-545 mg / d的蛋白排泄(A Manihot对losartan的P = 0.003,联合治疗对losartan的P <0.001)。平均eGFR没有明显变化。 3组不良反应发生率无差异(P> 0.05),各组均无严重不良反应发生。局限性结果不能推广到肾病综合征或eGFR降低的患者。结论对于患有中度蛋白尿的原发性肾脏疾病(1-2岁的慢性肾脏疾病)患者,Manihot是一种有前途的疗法。

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