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Types of 23S Ribosomal RNA Point Mutations and Therapeutic Outcomes for Helicobacter pylori
Sang Yoon Kim1, Jae Myung Park1,2, Chul-Hyun Lim3
1Division of Gastroenterology, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea.
Point mutations in Helicobacter pylori 23S rRNA gene impact clarithromycin resistance. Bismuth-quadruple therapy significantly improves eradication rates for patients with A2143G or double mutations.
Area of Science:
- Microbiology
- Genetics
- Pharmacology
Background:
- Point mutations in the 23S ribosomal RNA gene are linked to *Helicobacter pylori* clarithromycin resistance.
- Understanding these mutations is crucial for effective *H. pylori* eradication therapy.
Purpose of the Study:
- To determine the prevalence of 23S rRNA gene point mutations in *H. pylori*.
- To evaluate the efficacy of different eradication therapies based on mutation status.
Main Methods:
- Retrospective analysis of 464 patients undergoing *H. pylori* testing via multiplex PCR.
- Comparison of standard triple therapy versus bismuth-quadruple therapy in patients with and without specific 23S rRNA gene mutations (A2142G, A2143G).
Main Results:
- No significant difference in eradication rates between therapies for mutation-negative or A2142G mutation patients.
- Bismuth-quadruple therapy showed significantly higher eradication rates (25.8% vs 92.1% per-protocol) for A2143G or double mutations compared to standard triple therapy (24.2% vs 85.2% intention-to-treat).
Conclusions:
- The A2143G point mutation is a primary driver of clarithromycin resistance in *H. pylori*.
- Bismuth-quadruple therapy is demonstrably superior to standard triple therapy for *H. pylori* eradication in patients with A2143G or double 23S rRNA gene mutations.
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