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Bifidobacterium breve Irritable Bowel Syndrome (IBS)

D

Limited data from small studies. Preliminary evidence for symptom improvement.

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D

結論

Limited data from small studies. Preliminary evidence for symptom improvement.

Key Study Findings

Review
Compendium of Bifidobacterium-based probiotics: characteristics and therapeutic impact on human diseases.
Dose: None vs: None Outcome: None 効果: None None

対象集団: None

Other n=1098 8 weeks Open-label
A multicenter real-world, open-label study assessing the impact of a probiotic mixture on symptoms of …
Dose: None vs: None (single-arm open-label) Outcome: Treatment success for abdominal pain and bloating 効果: 73% pain, 81.9% bloating success at T1 <0.001

対象集団: IBS patients from 52 Italian gastroenterologists

Randomized Controlled Trial n=61 8 weeks Double-blind
Eight weeks of treatment with probiotic Bifidobacterium breve, Bif195 lowers fatigue scores in patients with …
Dose: None vs: Placebo Outcome: IBS-SSS symptom severity score change 効果: None None

対象集団: Patients with moderate-severe diarrhea-predominant IBS

Randomized Controlled Trial 4 weeks
Efficacy of Quadruple-coated Probiotics in Patients With Irritable Bowel Syndrome: A Randomized, Double-blind, Placebo-controlled, Parallel-group …
Dose: 2 g vs: Placebo Outcome: Constipation symptoms 効果: None P = 0.005

対象集団: IBS patients

Review
Postbiotics: A new member in the biotics family.
Dose: None vs: None Outcome: Clinical applications overview 効果: None None

対象集団: General population (review)

In Vitro
Bowel Inflammation and Nutrient Supplementation: Effects of a Fixed Combination of Probiotics, Vitamins, and Herbal …
Dose: None vs: None Outcome: Colitis severity 効果: None None

対象集団: Crohn's disease patients

Key Statistics

2

研究数

150

参加者数

Positive

D

グレード

Referenced Papers

Archivos argentinos de … 2024 3 件の引用
Journal of clinical … 2004 205 件の引用

Dosage & Usage

mg = milligrams · mcg = micrograms (1,000× smaller) · IU = International Units

一般的な使用量

general:
1-10 billion CFU/day
adultgisupport:
5-10 billion CFU/day
neonatalsupport:
1-5 billion CFU/day (as directed by pediatrician)

上限量: Well-tolerated up to 10 billion CFU/day in clinical trials

研究で検討された用量

用量 期間 効果 N
None -- Mixed --
None 8 weeks Positive 1098
None 8 weeks Neutral 61
2 g 4 weeks Mixed --
None -- Positive --
None -- Positive --
Serum-derived bovine immunoglobulin (SBI) -- Positive --
None -- Positive --

推奨摂取タイミング: Before meals or on empty stomach; for infants, mix with breast milk or formula

Safety & Side Effects

報告されている副作用

  • Mild gas during initial use
  • Occasional loose stools in infants (transient)
  • Rare abdominal discomfort
  • Very rare: bacteremia in immunocompromised individuals

既知の相互作用

  • Antibiotics (may reduce probiotic viability; space dosing 2 hours apart)
  • Immunosuppressants (use with caution in immunocompromised patients)

耐容上限摂取量: Well-tolerated up to 10 billion CFU/day in clinical trials

サプリメントの摂取を開始する前に、必ず医療専門家にご相談ください。

Frequently Asked Questions

Does Bifidobacterium breve help with Irritable Bowel Syndrome (IBS)?
Based on 2 studies with 150 participants, there is preliminary evidence that needs more research that Bifidobacterium breve may support Irritable Bowel Syndrome (IBS) management. Our evidence grade is D (Very Early Research).
How much Bifidobacterium breve should I take for Irritable Bowel Syndrome (IBS)?
Studies have used various dosages. A commonly studied range is 1-10 billion CFU/day. Always consult your healthcare provider before starting any supplement regimen.
Are there side effects of Bifidobacterium breve?
Reported side effects may include Mild gas during initial use, Occasional loose stools in infants (transient), Rare abdominal discomfort, Very rare: bacteremia in immunocompromised individuals. Most side effects are mild and dose-dependent. Consult your doctor if you experience any adverse reactions.
How strong is the evidence for Bifidobacterium breve and Irritable Bowel Syndrome (IBS)?
We rate the evidence as Grade D (Very Early Research). This rating is based on 2 peer-reviewed studies with 150 total participants. The overall direction of effect is positive.

Related Evidence

FDAに関する免責事項: これらの記述は米国食品医薬品局(FDA)による評価を受けていません。本ウェブサイトの製品および情報は、疾病の診断、治療、治癒、または予防を目的としたものではありません。表示されているエビデンスグレードは、公開された査読済み研究の分析に基づいており、医療上の助言を構成するものではありません。サプリメントの摂取を開始する前に、必ず医療専門家にご相談ください。