Bacillus coagulans: a viable adjunct therapy for relieving symptoms of rheumatoid arthritis according to a randomized, controlled trial
- 2010-01-12
- BMC Complementary and Alternative Medicine 10(1)
- D. Mandel
- K. Eichas
- J. Holmes
- PubMed: 20067641
- DOI: 10.1186/1472-6882-10-1
Study Design
- Type
- Randomized Controlled Trial (RCT)
- Sample size
- n = 45
- Population
- Patients with rheumatoid arthritis
- Methods
- Randomized Controlled Trial
- Highly Cited
- Rigorous Journal
Abstract
Background: Lactic acid-producing bacteria (LAB) probiotics demonstrate immunomodulating and anti-inflammatory effects and the ability to lessen the symptoms of arthritis in both animals and humans. This randomized, double-blind, placebo-controlled, parallel-design, clinical pilot trial was conducted to evaluate the effects of the LAB probiotic preparation, Bacillus coagulans GBI-30, 6086, on symptoms and measures of functional capacity in patients with rheumatoid arthritis (RA) in combination with pharmacological anti-arthritic medications.
Methods: Forty-five adult men and women with symptoms of RA were randomly assigned to receive Bacillus coagulans GBI-30, 6086 or placebo once a day in a double-blind fashion for 60 days in addition to their standard anti-arthritic medications. Arthritis activity was evaluated by clinical examination, the American College of Rheumatology (ACR) criteria, the Stanford Health Assessment Questionnaire Disability Index (HAQ-DI), and laboratory tests for erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP).
Results: Subjects who received Bacillus coagulans GBI-30, 6086 experienced borderline statistically significant improvement in the Patient Pain Assessment score (P = .052) and statistically significant improvement in Pain Scale (P = .046) vs placebo. Compared with placebo, Bacillus coagulans GBI-30, 6086 treatment resulted in greater improvement in patient global assessment and self-assessed disability; reduction in CRP; as well as the ability to walk 2 miles, reach, and participate in daily activities. There were no treatment-related adverse events reported throughout this study.
Conclusions: Results of this pilot study suggest that adjunctive treatment with Bacillus coagulans GBI-30, 6086 LAB probiotic appeared to be a safe and effective for patients suffering from RA. Because of the low study population size, larger trials are needed to verify these results.
Trial registration: ACTRN12609000435280.
Research Insights
participate in daily activities
- Effect
- Beneficial
- Effect size
- Small
- Dose
- once a day
Compared with placebo, Bacillus coagulans GBI-30, 6086 treatment resulted in greater improvement in patient global assessment
- Effect
- Beneficial
- Effect size
- Small
- Dose
- once a day
the ability to ... reach
- Effect
- Beneficial
- Effect size
- Small
- Dose
- once a day
Compared with placebo, Bacillus coagulans GBI-30, 6086 treatment resulted in greater improvement in ... self-assessed disability
- Effect
- Beneficial
- Effect size
- Small
- Dose
- once a day
the ability to walk 2 miles
- Effect
- Beneficial
- Effect size
- Small
- Dose
- once a day
Bacillus coagulans GBI-30, 6086 treatment resulted in greater improvement in patient global assessment and self-assessed disability; reduction in CRP; as well as the ability to walk 2 miles, reach, and participate in daily activities.
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- once a day
laboratory tests for erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP). (No significant difference reported for ESR in results.)
- Effect
- Neutral
- Effect size
- Small
- Dose
- once a day
Subjects who received Bacillus coagulans GBI-30, 6086 experienced borderline statistically significant improvement in the Patient Pain Assessment score (P = .052)
- Effect
- Neutral
- Effect size
- Small
- Dose
- once a day
statistically significant improvement in Pain Scale (P = .046) vs placebo
- Effect
- Beneficial
- Effect size
- Small
- Dose
- once a day
Adverse Events Reported
There were no treatment-related adverse events reported throughout this study.
- Finding
- Reported