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Assessment of a novel method to detect clarithromycin-resistant Helicobacter pylori using a stool antigen test reagent
BACKGROUND: The resistance rate of Helicobacter pylori to clarithromycin (CAM) is high among infected children in Japan. Therefore, a new method for detecting CAM-resistant H. pylori using a minimally invasive technique is strongly desired. We aimed to investigate the clinical usefulness of our newl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682763/ https://www.ncbi.nlm.nih.gov/pubmed/33228552 http://dx.doi.org/10.1186/s12876-020-01549-9 |
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author | Kakiuchi, Toshihiko Hashiguchi, Kazutoshi Imamura, Ichiro Nakayama, Aiko Takamori, Ayako Okuda, Masumi Matsuo, Muneaki |
author_facet | Kakiuchi, Toshihiko Hashiguchi, Kazutoshi Imamura, Ichiro Nakayama, Aiko Takamori, Ayako Okuda, Masumi Matsuo, Muneaki |
author_sort | Kakiuchi, Toshihiko |
collection | PubMed |
description | BACKGROUND: The resistance rate of Helicobacter pylori to clarithromycin (CAM) is high among infected children in Japan. Therefore, a new method for detecting CAM-resistant H. pylori using a minimally invasive technique is strongly desired. We aimed to investigate the clinical usefulness of our newly developed nested polymerase chain reaction-quenching probe (Nested PCR-QP) method using stool specimens. METHODS: We first evaluated our method using a residual solution of the H. pylori stool antigen test for adolescents. Then, we evaluated our method using culture testing for adults. RESULTS: Among 57 middle school students with H. pylori, the Nested PCR-QP test results of 53 (90.3%) were able to be analyzed. A total of 28 students had CAM resistance mutations. We found a genetic mutation in 28 students and no mutation in 23 students, and these results were consistent with those of PCR-direct sequencing. In the 23 adults who were diagnosed with H. pylori infection using the rapid urease test and culture testing, we were able to use Nested PCR-QP for analyzing 21 adults who tested positive in the stool H. pylori antigen test. The results obtained for all 21 adults were consistent with those obtained via the drug susceptibility test. CONCLUSIONS: Our novel method could be useful for non-invasively detecting CAM resistance mutations in H. pylori. This may help select a drug to reduce eradication failure rates against H. pylori. Trial registration This study was registered with the University Hospital Medical Information Network Clinical Trials Registry (no. UMIN000030632, https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034977) on 29 December 2017. |
format | Online Article Text |
id | pubmed-7682763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76827632020-11-24 Assessment of a novel method to detect clarithromycin-resistant Helicobacter pylori using a stool antigen test reagent Kakiuchi, Toshihiko Hashiguchi, Kazutoshi Imamura, Ichiro Nakayama, Aiko Takamori, Ayako Okuda, Masumi Matsuo, Muneaki BMC Gastroenterol Technical Advance BACKGROUND: The resistance rate of Helicobacter pylori to clarithromycin (CAM) is high among infected children in Japan. Therefore, a new method for detecting CAM-resistant H. pylori using a minimally invasive technique is strongly desired. We aimed to investigate the clinical usefulness of our newly developed nested polymerase chain reaction-quenching probe (Nested PCR-QP) method using stool specimens. METHODS: We first evaluated our method using a residual solution of the H. pylori stool antigen test for adolescents. Then, we evaluated our method using culture testing for adults. RESULTS: Among 57 middle school students with H. pylori, the Nested PCR-QP test results of 53 (90.3%) were able to be analyzed. A total of 28 students had CAM resistance mutations. We found a genetic mutation in 28 students and no mutation in 23 students, and these results were consistent with those of PCR-direct sequencing. In the 23 adults who were diagnosed with H. pylori infection using the rapid urease test and culture testing, we were able to use Nested PCR-QP for analyzing 21 adults who tested positive in the stool H. pylori antigen test. The results obtained for all 21 adults were consistent with those obtained via the drug susceptibility test. CONCLUSIONS: Our novel method could be useful for non-invasively detecting CAM resistance mutations in H. pylori. This may help select a drug to reduce eradication failure rates against H. pylori. Trial registration This study was registered with the University Hospital Medical Information Network Clinical Trials Registry (no. UMIN000030632, https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034977) on 29 December 2017. BioMed Central 2020-11-23 /pmc/articles/PMC7682763/ /pubmed/33228552 http://dx.doi.org/10.1186/s12876-020-01549-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Technical Advance Kakiuchi, Toshihiko Hashiguchi, Kazutoshi Imamura, Ichiro Nakayama, Aiko Takamori, Ayako Okuda, Masumi Matsuo, Muneaki Assessment of a novel method to detect clarithromycin-resistant Helicobacter pylori using a stool antigen test reagent |
title | Assessment of a novel method to detect clarithromycin-resistant Helicobacter pylori using a stool antigen test reagent |
title_full | Assessment of a novel method to detect clarithromycin-resistant Helicobacter pylori using a stool antigen test reagent |
title_fullStr | Assessment of a novel method to detect clarithromycin-resistant Helicobacter pylori using a stool antigen test reagent |
title_full_unstemmed | Assessment of a novel method to detect clarithromycin-resistant Helicobacter pylori using a stool antigen test reagent |
title_short | Assessment of a novel method to detect clarithromycin-resistant Helicobacter pylori using a stool antigen test reagent |
title_sort | assessment of a novel method to detect clarithromycin-resistant helicobacter pylori using a stool antigen test reagent |
topic | Technical Advance |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682763/ https://www.ncbi.nlm.nih.gov/pubmed/33228552 http://dx.doi.org/10.1186/s12876-020-01549-9 |
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