Probiotic containing Lactobacillus reuteri DSM 17648 as an adjunct treatment for Helicobacter pylori infection: A randomized, double‐blind, placebo‐controlled trial

Author:

Ismail Nur Izreena1,Nawawi Khairul Najmi Muhammad12,Hsin Deborah Chew Chia12,Hao Kok Wei1,Mahmood Nik Ritza Kosai Nik23,Chearn Gary Lee Chong1,Wong Zhiqin4,Tamil Azmi Mohd5,Joseph Hazel6,Raja Ali Raja Affendi127

Affiliation:

1. Gastroenterology Unit, Department of Medicine, Faculty of Medicine Universiti Kebangsaan Malaysia Kuala Lumpur Malaysia

2. GUT Research Group, Faculty of Medicine Universiti Kebangsaan Malaysia Kuala Lumpur Malaysia

3. Minimally Invasive, Upper Gastrointestinal and Bariatric Surgery Unit, Department of Surgery, Faculty of Medicine Universiti Kebangsaan Malaysia Kuala Lumpur Malaysia

4. Pantai Hospital Kuala Lumpur Malaysia

5. Department of Community Health, Faculty of Medicine Universiti Kebangsaan Malaysia Kuala Lumpur Malaysia

6. Y.S.P. Industries (M) Sdn. Bhd Kuala Lumpur Malaysia

7. School of Medical and Life Sciences Sunway University Selangor Malaysia

Abstract

AbstractBackgroundDespite multiple therapy regimens, the decline in the Helicobacter pylori eradication rate poses a significant challenge to the medical community. Adding Lactobacillus reuteri probiotic as an adjunct treatment has shown some promising results. This study aims to investigate the efficacy of Lactobacillus reuteri DSM 17648 in H. pylori eradication and its effect in ameliorating gastrointestinal symptoms and adverse treatment effects.Materials and MethodsThis randomized, double‐blinded, placebo‐controlled trial involved treatment‐naïve H. pylori‐positive patients. Ninety patients received standard triple therapy for 2 weeks before receiving either a probiotic or placebo for 4 weeks. The posttreatment eradication rate was assessed via a 14C urea breath test in Week 8. The Gastrointestinal Symptom Rating Scale (GSRS) questionnaire and an interview on treatment adverse effects were conducted during this study.ResultsThe eradication rate was higher in the probiotic group than in the placebo group, with a 22.2% difference in the intention‐to‐treat analysis (91.1% vs. 68.9%; p = 0.007) and 24.3% difference in the per‐protocol analysis (93.2% vs. 68.9%; p = 0.007). The probiotic group showed significant pre‐ to post‐treatment reductions in indigestion, constipation, abdominal pain, and total GSRS scores. The probiotic group showed significantly greater reductions in GSRS scores than the placebo group: indigestion (4.34 ± 5.00 vs. 1.78 ± 5.64; p = 0.026), abdominal pain (2.64 ± 2.88 vs. 0.89 ± 3.11; p = 0.007), constipation (2.34 ± 3.91 vs. 0.64 ± 2.92; p = 0.023), and total score (12.41 ± 12.19 vs. 4.24 ± 13.72; p = 0.004). The probiotic group reported significantly fewer adverse headache (0% vs. 15.6%; p = 0.012) and abdominal pain (0% vs. 13.3%; p = 0.026) effects.ConclusionsThere was a significant increase in H. pylori eradication rate and attenuation of symptoms and adverse treatment effects when L. reuteri was given as an adjunct treatment.

Funder

Marathon

Publisher

Wiley

Subject

Infectious Diseases,Gastroenterology,General Medicine

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