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首页> 外文期刊>Journal of digestive diseases >Impact of a probiotic product on bowel habits and microbial profile in participants with functional constipation: A randomized controlled trial
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Impact of a probiotic product on bowel habits and microbial profile in participants with functional constipation: A randomized controlled trial

机译:益生菌产品对功能性便秘参与者的肠习惯和微生物概况的影响:随机对照试验

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Objective To investigate the clinical efficacy of a multi‐strain probiotic product on bowel habits and microbial profile in participants with functional constipation. Methods This was a randomized, double‐blind, placebo‐controlled and parallel‐arm study. Altogether 94 otherwise healthy adults aged 18 to 65?years with symptoms of functional constipation were randomized as part of the intention‐to‐treat population. The participants received a placebo or the probiotic product (1.5?×?10 10 CFU/day), consisting of Lactobacillus acidophilus DDS‐1, Bifidobacterium animalis subsp. lactis UABla‐12, Bifidobacterium longum UABl‐14 and Bifidobacterium bifidum UABb‐10 over 4?weeks. Outcomes included the patient assessment of constipation‐symptom (PAC‐SYM) questionnaire, stool frequency and consistency, and microbial profile. Results There were no significant between‐group differences in the PAC‐SYM score, despite significant within‐group differences ( P ??0.001) over the study period. The probiotic group showed a faster normalization of stool frequency and consistency, with most participants achieving a normalized profile after 1?week. Fecal samples of the probiotic group exhibited higher relative abundance of Ruminococcaceae ( P = 0.0047), including the Ruminococcus genus, and lower relative abundance of Erysipelotrichaceae ( P = 0.0172) at end‐point compared with baseline. Placebo group samples showed similar abundance profiles over the study, with the exception of Clostridiaceae, which was lower at the study end‐point ( P = 0.0033). Among treated participants, all four probiotic strains were significantly more abundant after the intervention. Conclusions No significant differences were observed in symptomology, with both groups showing a more than 20% improvement. However, the probiotic helped modulate bowel function earlier than the placebo, with a corresponding shift to a more fibrolytic microbiota.
机译:目的探讨多重菌株益生菌产品对功能性便秘参与者肠习惯和微生物谱的临床疗效。方法这是随机,双盲,安慰剂控制和平行的臂研究。总共94否否则健康成年人18至65岁?患有功能性便秘症状的年份作为意向治疗人口的一部分随机化。参与者接受了安慰剂或益生菌产品(1.5?×10 10 CFU /天),由乳杆菌酸酐DDS-1,双歧杆菌患者组成。 Lactis Uabla-12,长双歧杆菌UAB1-14和双歧杆菌UABB-10超过4?周。结果包括患者评估便秘 - 症状(PAC-SYM)问卷,大便频率和一致性和微生物轮廓。结果在研究期间内部差异(p≤j≤0.001),PAC-符号评分中没有显着的差异。益生菌组表现出粪便频率和一致性的速度较快,大多数参与者在1个星期后实现了归一化的概况。益生菌组的粪便样品表现出更高的钻杆状曲霉(P = 0.0047),包括逆转带的喇叭心能属,以及终点的肝功能率低(P = 0.0172)的较低相对丰度。安慰剂组样本在研究中显示出类似的丰富型材,除了蛋白质末端的蛋白质,在研究终点(P = 0.0033)下降。在治疗的参与者中,干预后,所有四种益生菌菌株明显更加丰富。结论在症状中没有观察到显着差异,两组均具有20%以上的改善。然而,益生菌有助于调节比安慰剂更早的排便,相应的转变为更纤维溶解的微生物群。

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