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一项随机、双盲、安慰剂对照的临床研究,以评估BC99治疗成人慢性便秘的疗效和安全性。

A randomized, double-blind, placebo-controlled clinical study to evaluate the efficacy and safety of BC99 in the treatment of chronic constipation in adults.

作者信息

Wu Ying, Bai Zhouya, Jin Yuehong, Zhu Hong, Dong Yao, Gu Shaobin, Jin Ying

机构信息

College of Food and Bioengineering, Henan University of Science and Technology, Luoyang, China.

Henan Engineering Research Center of Food Microbiology, Luoyang, China.

出版信息

Front Nutr. 2024 Jul 25;11:1395083. doi: 10.3389/fnut.2024.1395083. eCollection 2024.

Abstract

INTRODUCTION

has emerged as a promising candidate for the management of gastrointestinal ailments. The novel strain of , BC99 (BC99), displays robust pathogen-inhibiting capabilities, susceptibility to various antibiotics, and a high level of biosafety. Nevertheless, additional research is necessary to fully understand its effectiveness in managing chronic constipation.

METHODS

This study investigates the role of BC99 in alleviating chronic constipation in a double-blind, placebo-controlled, randomized trial, and participants were divided into BC99 (2 billion CFU/d) or placebo (maltodextrin) groups for a 4-week period.

RESULTS AND DISCUSSION

Results showed that significant improvements were noted in the BC99 group, with an increase in complete spontaneous bowel movements (CSBM) after 4-week treatment compared to the placebo ( = 0.002). The BC99 group also showed significantly lower Quality of Life (PAC-QOL) scores and reduced Constipation Symptoms (PAC-SYM) scores after 4 weeks of treatment ( < 0.001), indicating symptomatic relief. Notably, BC99 effectively modulated key gut microbiota such as and , linked to crucial metabolic pathways like glutathione metabolism. In all, BC99 is confirmed to be an effective and safe therapeutic option for the relief of adult chronic constipation, enhancing gut microbiota balance and influencing critical metabolic pathways.

CLINICAL TRIAL REGISTRATION

ChiCTR2200065493.

摘要

引言

已成为治疗胃肠道疾病的一个有前景的候选方案。新型菌株BC99,表现出强大的病原体抑制能力、对多种抗生素的敏感性以及高度的生物安全性。然而,需要更多研究来全面了解其在治疗慢性便秘方面的有效性。

方法

本研究在一项双盲、安慰剂对照、随机试验中调查了BC99在缓解慢性便秘中的作用,参与者被分为BC99(20亿CFU/天)组或安慰剂(麦芽糊精)组,为期4周。

结果与讨论

结果显示,BC99组有显著改善,与安慰剂相比,4周治疗后完全自主排便(CSBM)增加(P = 0.002)。治疗4周后,BC99组的生活质量(PAC-QOL)评分和便秘症状(PAC-SYM)评分也显著降低(P < 0.001),表明症状得到缓解。值得注意的是,BC99有效地调节了关键肠道微生物群,如与谷胱甘肽代谢等关键代谢途径相关的[具体微生物名称未给出]和[具体微生物名称未给出]。总之,BC99被证实是缓解成人慢性便秘的一种有效且安全的治疗选择,可增强肠道微生物群平衡并影响关键代谢途径。

临床试验注册

ChiCTR2200065493。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb7c/11306189/e45a35cd531e/fnut-11-1395083-g001.jpg

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