School of Food Science and Nutrition, University of Leeds, Leeds, UK.
Probiotics Antimicrob Proteins. 2020 Sep;12(3):834-839. doi: 10.1007/s12602-019-09609-7.
Probiotics, specifically Bifidobacteria, may improve abdominal pain in patients with irritable bowel syndrome (IBS); however, results from randomised controlled trials (RCTs) are conflicting. Here, we systematically reviewed the efficacy of Bifidobacteria on abdominal pain in IBS. We searched MEDLINE, EMBASE and the Cochrane Controlled Trials Register from inception to 20 May 2019, without language or date restrictions. The search strategy comprised of the combination of three concepts: supplementation, abdominal pain, and IBS. Inclusion criteria included double-blind placebo-controlled RCTs featuring Bifidobacteria supplementation in Rome-diagnosed IBS patients. A total of 8 RCTs involving a total of 1045 patients with Rome diagnosed IBS were included. The dose of total Bifidobacteria ranged from 10 to > 10 cfu (colony-forming unit) and duration of supplementation ranged between 2 and 8 weeks. Bifidobacteria was delivered through either intake of fermented milk products, encapsulation or via a malted milk beverage, with all studies assessing abdominal pain via a visual analogue Likert scale. From the studies included, 50% (n = 4) of studies found a statistically significant improvement in abdominal pain following Bifidobacteria supplementation compared to placebo, 38% (n = 3) of studies found non-significant improvements and 12% (n = 1) showed a statistically significant dose-response effect of improvement. The evidence shows a heterogeneity of effect for Bifidobacteria dependent upon strain, dosage and delivery method. While not all studies demonstrate significant improvements in abdominal pain, none of the selected studies reported an increase in pain or other adverse effects.
益生菌,特别是双歧杆菌,可能改善肠易激综合征(IBS)患者的腹痛症状;然而,随机对照试验(RCT)的结果存在矛盾。在此,我们系统地回顾了双歧杆菌对 IBS 腹痛的疗效。我们检索了 MEDLINE、EMBASE 和 Cochrane 对照试验登记处,检索时间截至 2019 年 5 月 20 日,未对语言或日期进行限制。检索策略包括三个概念的组合:补充剂、腹痛和 IBS。纳入标准包括双歧杆菌补充剂治疗罗马诊断的 IBS 患者的双盲安慰剂对照 RCT。共纳入 8 项 RCT,共计 1045 例罗马诊断的 IBS 患者。双歧杆菌的总剂量范围为 10-10 cfu(菌落形成单位),补充时间为 2-8 周。双歧杆菌通过摄入发酵乳制品、封装或麦芽乳饮料进行递送,所有研究均通过视觉模拟 Likert 量表评估腹痛。在纳入的研究中,50%(n=4)的研究发现双歧杆菌补充剂治疗后腹痛明显改善,与安慰剂相比有统计学意义,38%(n=3)的研究发现无显著改善,12%(n=1)的研究显示改善存在统计学意义的剂量反应效应。证据表明双歧杆菌的作用效果存在异质性,取决于菌株、剂量和递送方法。虽然并非所有研究都表明腹痛有显著改善,但所选研究均未报告疼痛或其他不良反应增加。