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Title: | Bacillus subtilis (bg01-4tm) improves self-reported symptoms for constipation, indigestion, and dyspepsia: a phase 1/2a randomized controlled trial. | Authors: | Patch C.;Pearce A.J.;Cheng M.;Boyapati R.;Brenna J.T. | Monash Health Department(s): | Gastroenterology and Hepatology | Institution: | (Patch, Pearce) School Allied Health, Human Services and Sport, Melbourne 3086, Australia (Patch, Cheng, Brenna) Adepa Lifesciences, Melbourne 3000, Australia (Boyapati) Department of Gastroenterology, Monash Health, Melbourne 3977, Australia (Boyapati) Faculty of Medicine, Nursing and Health Science, Monash University, Melbourne 3800, Australia (Brenna) Division of Nutritional Sciences, Cornell University, Ithaca, NY 14853, United States (Brenna) Dell Paediatric Research Institute, Department of Paediatrics, of Nutrition, and of Chemistry, University of Texas at Austin, Austin, TX 78712, United States |
Issue Date: | 28-Nov-2023 | Copyright year: | 2023 | Publisher: | Multidisciplinary Digital Publishing Institute (MDPI) | Place of publication: | Switzerland | Publication information: | Nutrients. 15(21) (no pagination), 2023. Article Number: 4490. Date of Publication: November 2023. | Journal: | Nutrients | Abstract: | Background: Functional gastrointestinal disorders (FGIDs) are common, difficult-to-manage conditions. Probiotics are emerging as a dietary component that influence gastrointestinal (GI) health. We conducted a double-blinded randomised controlled trial of a proprietary strain of deactivated Bacillus subtilis (BG01-4TM) high in branched-chain fatty acids (BCFA) to treat self-reported FGID. Method(s): Participants (n = 67) completed a four-week intervention of BG01-4TM (n = 34) or placebo (n = 33). The Gastrointestinal Symptom Rating Scale (GSRS) served as the outcome measure, collected prior to, at two weeks, and at four weeks after completion of the intervention. Result(s): At four weeks, one of three primary outcomes, constipation in the experimental group, was improved by 33% compared to placebo (15%); both other primary outcomes, Total GSRS and diarrhoea, were significantly improved in both the experimental and placebo groups (32%/26% and 20%/22%, respectively). The pre-planned secondary outcome, indigestion, was improved at four weeks (32%) but compared to the placebo (21%) was not significant (p = 0.079). Exploratory analysis, however, revealed that clusters for constipation (18% improvement, p < 0.001), indigestion (11% improvement, p = 0.04), and dyspepsia (10% improvement, p = 0.04) were significantly improved in the intervention group compared to the placebo. Conclusion(s): These initial findings suggest that in people with self-reported FGID, BG01-4TM improves specific symptoms of constipation and related GI dysfunction. Longer-term confirmatory studies for this intervention are warranted. Trial registration: This study was registered prospectively (25 October 2021) at the Australian New Zealand Clinical Trials Registry (ACTRN12621001441808p).Copyright © 2023 by the authors. | DOI: | http://monash.idm.oclc.org/login?url=https://dx.doi.org/10.3390/nu15214490 | PubMed URL: | 37960143 [https://www.ncbi.nlm.nih.gov/pubmed/?term=37960143] | URI: | https://repository.monashhealth.org/monashhealthjspui/handle/1/50887 | Type: | Article | Subjects: | Bacillus subtilis dyspepsia gastrointestinal symptoms probiotic |
Type of Clinical Study or Trial: | Randomised controlled trial |
Appears in Collections: | Articles |
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