Detection of Clarithromycin Resistance in Helicobacter pylori Using the AllplexTM H. pylori & ClariR Assay and the Ezplex® HP-CLA Real-Time PCR Kit.

Tae-Woo Kim, Won Seok Lee, Dong Jin Yoon, Ilsoo Kim, Joon Sung Kim
{"title":"Detection of Clarithromycin Resistance in Helicobacter pylori Using the AllplexTM H. pylori & ClariR Assay and the Ezplex® HP-CLA Real-Time PCR Kit.","authors":"Tae-Woo Kim, Won Seok Lee, Dong Jin Yoon, Ilsoo Kim, Joon Sung Kim","doi":"10.7704/kjhugr.2024.0070","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>The success of Helicobacter pylori eradication using clarithromycin-based triple therapy relies on the bacteria being sensitive to clarithromycin. This study evaluated the diagnostic performance of two frequently used polymerase chain reaction (PCR) methods (AllplexTM H. pylori & ClariR Assay [Seegene] and Ezplex® HP-CLA Real-time PCR [SML Genetree]) to detect H. pylori infection and identify point mutations associated with clarithromycin resistance.</p><p><strong>Methods: </strong>Patients who underwent esophagogastroduodenoscopy between August 2023 and April 2024 at Incheon St. Mary's Hospital were enrolled in this study. The diagnostic performance of the Allplex method was evaluated against the rapid urease test (RUT), culture, and Ezplex HP-CLA methods. Point mutation detection using the Allplex and Ezplex methods was compared with the results of gene sequencing. The rates of H. pylori eradication following Ezplex-based tailored therapy were also analyzed.</p><p><strong>Results: </strong>Eighty-seven gastric biopsy specimens were analyzed. For diagnosing H. pylori infections, Allplex demonstrated kappa values of 0.670 compared with RUT, 0.468 compared with culture, and 0.880 compared with Ezplex. Among the 87 bacterial isolates subjected to gene sequencing to detect clarithromycin resistance-associated point mutations, the Allplex and Ezplex methods demonstrated 74 and 76 concordant results, respectively. The H. pylori eradication rate using Ezplex-based tailored therapy was 90.7%.</p><p><strong>Conclusions: </strong>This study demonstrated that both the Allplex and Ezplex methods are helpful for diagnosing H. pylori infections and detecting clarithromycin resistance. Furthermore, the Ezplex method was clinically effective for guiding tailored therapy to yield successful H. pylori eradication.</p>","PeriodicalId":520887,"journal":{"name":"The Korean journal of helicobacter and upper gastrointestinal research","volume":"25 1","pages":"42-47"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12173568/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Korean journal of helicobacter and upper gastrointestinal research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7704/kjhugr.2024.0070","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/7 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: The success of Helicobacter pylori eradication using clarithromycin-based triple therapy relies on the bacteria being sensitive to clarithromycin. This study evaluated the diagnostic performance of two frequently used polymerase chain reaction (PCR) methods (AllplexTM H. pylori & ClariR Assay [Seegene] and Ezplex® HP-CLA Real-time PCR [SML Genetree]) to detect H. pylori infection and identify point mutations associated with clarithromycin resistance.

Methods: Patients who underwent esophagogastroduodenoscopy between August 2023 and April 2024 at Incheon St. Mary's Hospital were enrolled in this study. The diagnostic performance of the Allplex method was evaluated against the rapid urease test (RUT), culture, and Ezplex HP-CLA methods. Point mutation detection using the Allplex and Ezplex methods was compared with the results of gene sequencing. The rates of H. pylori eradication following Ezplex-based tailored therapy were also analyzed.

Results: Eighty-seven gastric biopsy specimens were analyzed. For diagnosing H. pylori infections, Allplex demonstrated kappa values of 0.670 compared with RUT, 0.468 compared with culture, and 0.880 compared with Ezplex. Among the 87 bacterial isolates subjected to gene sequencing to detect clarithromycin resistance-associated point mutations, the Allplex and Ezplex methods demonstrated 74 and 76 concordant results, respectively. The H. pylori eradication rate using Ezplex-based tailored therapy was 90.7%.

Conclusions: This study demonstrated that both the Allplex and Ezplex methods are helpful for diagnosing H. pylori infections and detecting clarithromycin resistance. Furthermore, the Ezplex method was clinically effective for guiding tailored therapy to yield successful H. pylori eradication.

Abstract Image

Abstract Image

Abstract Image

应用AllplexTM H. pylori & ClariR Assay和Ezplex®HP-CLA Real-Time PCR Kit检测幽门螺杆菌克拉霉素耐药性
目的:基于克拉霉素的三联疗法根除幽门螺杆菌的成功依赖于对克拉霉素敏感的细菌。本研究评估了两种常用的聚合酶链反应(PCR)方法(AllplexTM H. pylori & ClariR Assay [Seegene]和Ezplex®HP-CLA Real-time PCR [SML Genetree])检测幽门螺杆菌感染和鉴定与克拉霉素耐药相关的点突变的诊断性能。方法:入选于2023年8月至2024年4月在仁川圣玛丽医院接受食管胃十二指肠镜检查的患者。将Allplex方法的诊断性能与快速脲酶试验(RUT)、培养和Ezplex HP-CLA方法进行比较。将Allplex法和Ezplex法的点突变检测结果与基因测序结果进行比较。同时分析了以ezplexs为基础的个体化治疗后幽门螺杆菌根除率。结果:对87例胃活检标本进行了分析。在诊断幽门螺杆菌感染方面,Allplex与RUT比较kappa值为0.670,与培养比较kappa值为0.468,与Ezplex比较kappa值为0.880。对87株分离菌株进行基因测序检测克拉霉素耐药相关点突变,Allplex法和Ezplex法的一致性结果分别为74和76。以ezplexs为基础的个体化治疗幽门螺杆菌根除率为90.7%。结论:Allplex法和Ezplex法均有助于诊断幽门螺杆菌感染和检测克拉霉素耐药性。此外,Ezplex方法在指导定制治疗以成功根除幽门螺杆菌方面具有临床效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信