Effect of Probiotic-Assisted Eradication of cagA+/ vacA s1m1 Helicobacter pylori on Intestinal Flora

Biomed Res Int. 2022 Apr 29:2022:8607671. doi: 10.1155/2022/8607671. eCollection 2022.

Abstract

Objective: We attempted to evaluate the effects of probiotic-assisted eradication of cytotoxin-associated gene A (cagA)+/vacuolating cytotoxin A (vacA) s1m1 Helicobacter pylori (H. pylori) on the intestinal flora, inflammatory factors, and clinical outcomes.

Methods: A total of 180 patients with cagA+/vacA s1m1 H. pylori were randomly divided into two groups. Group A was treated with bismuth quadruple therapy (BQT). Group B was treated with S. boulardii in addition to BQT. The distribution of intestinal flora, serum interleukin-8 (IL-8), IL-17, tumor necrosis factor-α (TNF-α) levels, recovery time of clinical symptoms, total effective rate of clinical symptoms, H. pylori eradication rate, and adverse reactions were observed.

Results: 2 weeks after treatment, the contents of Bifidobacterium, Bacteroides, and Lactobacillus in the intestinal tract of Group A decreased, while the amounts of Enterococcus and Enterobacter increased. In Group B, the contents of Bifidobacterium, Bacteroides, and Lactobacillus increased, while the amounts of Enterococcus and Enterobacter did not change significantly. Moreover, the trend of this flora change was still present at 4 weeks after treatment. Compared with Group A, Group B had lower IL-8, IL-17, and TNF-α levels, shorter recovery time of clinical symptoms, higher overall efficiency of clinical symptoms, and lower occurrence of adverse reactions. The eradication rate did not differ significantly between the two groups.

Conclusion: BQT can lead to intestinal flora disorders in cagA+/vacA s1m1 H. pylori patients. S. boulardii can improve the distribution of intestinal flora, downregulate immune-inflammatory mediators, and modify clinical symptoms in patients.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Antigens, Bacterial / genetics
  • Bacterial Proteins / genetics
  • Bismuth / therapeutic use
  • Cytotoxins
  • Gastrointestinal Microbiome*
  • Helicobacter Infections* / microbiology
  • Helicobacter pylori* / genetics
  • Humans
  • Interleukin-17 / therapeutic use
  • Interleukin-8
  • Probiotics* / therapeutic use
  • Tumor Necrosis Factor-alpha

Substances

  • Antigens, Bacterial
  • Bacterial Proteins
  • Cytotoxins
  • Interleukin-17
  • Interleukin-8
  • Tumor Necrosis Factor-alpha
  • Bismuth