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Effects of Brazilian green propolis on proteinuria and renal function in patients with chronic kidney disease: a randomized, double-blind, placebo-controlled trial

机译:巴西绿色蜂胶对慢性肾病患者蛋白尿和肾功能的影响:随机,双盲,安慰剂对照试验

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Chronic kidney disease (CKD) is a public health problem worldwide, and proteinuria is a well-established marker of disease progression in CKD patients. Propolis, a natural resin produced by bees from plant materials, has anti-inflammatory, immunomodulatory, and anti-oxidant properties, as well as having been shown to have an antiproteinuric effect in experimental CKD. The aim of this study was to evaluate the impact of Brazilian green propolis extract on proteinuria reduction and the changes in the estimated glomerular filtration rate (eGFR). This was a randomized, double-blind, placebo-controlled study including patients with CKD caused by diabetes or of another etiology, 18-90?years of age, with an eGFR of 25-70?ml/min per 1.73?m2?300?mg/g, respectively). We screened 148 patients and selected 32, randomly assigning them to receive 12?months of Brazilian green propolis extract at a dose of 500?mg/day (n?=?18) or 12?months of a placebo (n?=?14). At the end of treatment, proteinuria was significantly lower in the propolis group than in the placebo group-695?mg/24?h (95% CI, 483 to 999) vs. 1403?mg/24?h (95% CI, 1031 to 1909); P?=?0.004-independent of variations in eGFR and blood pressure, which did not differ between the groups during follow-up. Urinary monocyte chemoattractant protein-1 was also significantly lower in the propolis group than in the placebo group-58?pg/mg creatinine (95% CI, 36 to 95) vs. 98?pg/mg creatinine (95% CI, 62 to 155); P?=?0.038. Brazilian green propolis extract was found to be safe and well tolerated, as well as to reduce proteinuria significantly in patients with diabetic and non-diabetic CKD. ( ClinicalTrials.gov number NCT02766036. Registered: May 9, 2016).
机译:慢性肾病(CKD)是全球公共卫生问题,蛋白尿是CKD患者中疾病进展的良好标志。蜂胶是由植物材料生产的天然树脂,具有抗炎,免疫调节和抗氧化性能,以及已经显示在实验CKD中具有抗胰岛素效应。本研究的目的是评估巴西绿色蜂胶提取物对蛋白尿的影响,估计肾小球过滤速率(EGFR)的变化。这是一项随机,双盲,安慰剂对照研究,包括糖尿病或另一种病因引起的CKD患者,18-90岁,EGFR为25-70?ml / min / min / min / min / min每1.73?300分别是mg / g)。我们筛选了148名患者并选定32名,随机分配它们以获得12个月的巴西绿色蜂胶提取物,剂量为500?mg /天(n?=?18)或12?几个月的安慰剂(n?=?14 )。在治疗结束时,蛋白尿在蜂胶组中显着低于安慰剂组-695?Mg / 24?H(95%CI,483至999)与1403?Mg / 24?H(95%CI, 1031到1909年); p?= 0.004 - 与EGFR和血压的变化无关,在随访期间的组之间没有差异。丙醇组中的尿嘧t单核细胞化学蛋白-1也显着低于安慰剂组-58?PG / mg肌酐(95%CI,36至95)与98〜pg / mg肌酐(95%CI,62 155); p?=?0.038。发现巴西绿色蜂胶提取物是安全和耐受性的,以及糖尿病患者和非糖尿病CKD患者显着降低蛋白尿。 (ClinicalTrials.gov数字NCT02766036。注册:2016年5月9日)。

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