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Bifidobacterium Longum for IBS (Irritable Bowel Syndrome)
This pairing is unusual: the best trial of B. longum in IBS found its clearest benefit on mood rather than on bowel symptoms. If your IBS travels with anxiety or low mood, the case is more interesting than for IBS alone.
Overview
Verdict
B. longum NCC3001 produced a striking reduction in depression scores and measurable changes in brain activity in IBS patients, but its effect on IBS symptoms themselves was modest and inconsistent. It is a reasonable option when low mood accompanies IBS, and a weak one for gut symptoms alone.
How It Works
Dosing & Protocol
Typical dose
- Recommended dose
- 10 billion CFU daily
- Expected timeframe
- 4-6 weeks for mood measures; 8 weeks before judging bowel symptoms
Protocol
- dose
- 10 billion CFU once daily
- notes
- Use an enteric-protected capsule; this species is acid sensitive
- strain
- NCC3001 for the mood-and-IBS profile; BB536 for general regularity
- timing
- With a meal to buffer stomach acid
- duration
- 6-8 weeks
Evidence
What the studies say
Probiotic Bifidobacterium longum NCC3001 Reduces Depression Scores and Alters Brain Activity: A Pilot Study in Patients With Irritable Bowel Syndrome
Pinto-Sanchez MI, Hall GB, Ghajar K +1 more
B. longum NCC3001 reduced depression scores in IBS patients versus placebo at 6 weeks and altered limbic brain responses, but did not significantly reduce anxiety or core IBS symptoms.
Effect of Postbiotic Bifidobacterium longum CECT 7347 on Gastrointestinal Symptoms, Serum Biochemistry, and Intestinal Microbiota in Healthy Adults: A Randomised, Placebo-Controlled Pilot Study
Naghibi M, Pont-Beltran A, Lamelas A +2 more
While minimal changes were observed in gastrointestinal (GI) symptoms, the HT-ES1 group showed a significant decrease in total and non-HDL cholesterol compared to the placebo.
A randomized double-blind, placebo-controlled trial to evaluate the safety and efficacy of live Bifidobacterium longum CECT 7347 (ES1) and heat-treated Bifidobacterium longum CECT 7347 (HT-ES1) in participants with diarrhea-predominant irritable bowel syndrome
Srivastava S, Basak U, Naghibi M +2 more
The decrease in mean IBS-SSS score from baseline to Day 84 was: ES1 (-173.70) vs placebo (-60.44) (p < .0001).
Safety
Caveats
The headline mood result comes from a single 44-person trial with manufacturer involvement and has not been independently replicated. IBS symptom benefit specifically was not statistically significant in that trial.
Less likely to help if
Medical Disclaimer
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Individual results may vary. The statements on this website have not been evaluated by the Food and Drug Administration. Products and information are not intended to diagnose, treat, cure, or prevent any disease.