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

被引:19
作者
Ismail, Nur Izreena [1 ]
Nawawi, Khairul Najmi Muhammad [1 ,2 ]
Hsin, Deborah Chew Chia [1 ,2 ]
Hao, Kok Wei [1 ]
Mahmood, Nik Ritza Kosai Nik [2 ,3 ]
Chearn, Gary Lee Chong [1 ]
Wong, Zhiqin [4 ]
Tamil, Azmi Mohd [5 ]
Joseph, Hazel [6 ]
Ali, Raja Affendi Raja [1 ,2 ,7 ,8 ,9 ]
机构
[1] Univ Kebangsaan Malaysia, Fac Med, Dept Med, Gastroenterol Unit, Kuala Lumpur, Malaysia
[2] Univ Kebangsaan Malaysia, Fac Med, GUT Res Grp, Kuala Lumpur, Malaysia
[3] Univ Kebangsaan Malaysia, Fac Med, Upper Gastrointestinal & Bariatr Unit, Dept Surg,Minimally Invas, Kuala Lumpur, Malaysia
[4] Pantai Hosp, Kuala Lumpur, Malaysia
[5] Univ Kebangsaan Malaysia, Fac Med, Dept Community Hlth, Kuala Lumpur, Malaysia
[6] YSP Ind M Sdn Bhd, Kuala Lumpur, Malaysia
[7] Sunway Univ, Sch Med & Life Sci, Selangor, Malaysia
[8] Sunway Univ, Sch Med & Life Sci, Med, 5 Jalan Univ, Petaling Jaya 47500, Selangor, Malaysia
[9] Sunway Univ, Sch Med & Life Sci, 5 Jalan Univ, Petaling Jaya 47500, Selangor, Malaysia
关键词
eradication; gastrointestinal symptom rating scale; GSRS; Helicobacter pylori; Lactobacillus reuteri; probiotics; LACTOBACILLUS-REUTERI SUPPLEMENTATION; IN-VITRO; THERAPY; ERADICATION; INHIBITION; EFFICACY; VIVO;
D O I
10.1111/hel.13017
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Despite 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 Methods: This randomized, double-blinded, placebo-controlled trial involved treatment-naive 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 C-14 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.Results: The 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.Conclusions: There 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.
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页数:11
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