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首页> 外文期刊>Drug and Chemical Toxicology >Efficacy of probiotic supplementation on quality of life and pulmonary symptoms due to sulfur mustard exposure: a randomized double-blind placebo-controlled trial
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Efficacy of probiotic supplementation on quality of life and pulmonary symptoms due to sulfur mustard exposure: a randomized double-blind placebo-controlled trial

机译:益生菌补充对硫磺芥末暴露导致的生命质量和肺症状的疗效:随机双盲安慰剂对照试验

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摘要

Objective: This study investigated the efficacy and safety of supplementation with probiotics in improving chronic pulmonary symptoms due to sulfur mustard (SM) exposure. Methods: In a randomized double-blind placebo-controlled study, 65 subjects suffering from chronic pulmonary complications of SM were assigned to one probiotic capsule (1x10(9) CFU containing seven strains of lactic acid-producing bacteria) every 12h or an identical placebo for six weeks. Serum high-sensitivity C-reactive protein (CRP) concentrations, pulmonary function tests (FEV1, FEV1/FVC and MMEF 25-75%) and COPD assessment test (CAT) were assessed at baseline and at the end of trial. Results: The groups were comparable in baseline characteristics. There were significant improvements in FEV1/FVC in the probiotic but not in placebo group. CAT scores were decreased in both study groups. However, between-group comparison of changes in the assessed parameters reached statistical significance only for CAT score (p<0.001). There was no report of adverse events during the course of trial. Conclusions: Findings of the present trial favor the efficacy of probiotic supplementation in improving the pulmonary symptoms of SM-exposed subjects.
机译:目的:本研究调查了补充益生菌在提高硫芥末(SM)暴露时提高慢性肺症状的疗效和安全性。方法:在随机的双盲安慰剂对照研究中,每12h或相同安慰剂将65名患有SM的慢性肺并发症的受试者分配给一种益生菌胶囊(1×10(9)CFU)每12h或相同的安慰剂六周。在基线和试验结束时评估血清高敏感性C-反应蛋白(CRP)浓度,肺功能试验(FEV1,FEV1 / FVC和MMEF 25-75%)和COPD评估试验(CAT)。结果:该组在基线特征中具有可比性。益生菌中FEV1 / FVC的显着改善,但不在安慰剂组中。两项研究组中的猫分数减少。然而,在群体分数的评估参数的变化的比较之间的比较达到了肠比较(P <0.001)。审判过程中没有不良事件的报告。结论:目前试验的结果有利于益生菌补充在改善SM暴露受试者肺症状方面的疗效。

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