Cargando…

Clinical Evaluation of a Novel Stool Antigen Test Using Bioluminescent Enzyme Immunoassay for Detecting Helicobacter pylori

BACKGROUND: BLEIA ™ “EIKEN” Helicobacter pylori antigen (B[EIA]) is based on the bioluminescent enzyme immunoassay (BLEIA) method that was newly developed with high sensitivity in detecting Helicobacter pylori (H. pylori) antigen in feces. METHODS: In the project for H. pylori screening and treatmen...

Descripción completa

Detalles Bibliográficos
Autores principales: Kakiuchi, Toshihiko, Matsuo, Muneaki, Sakata, Yasuhisa, Fujimoto, Kazuma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050312/
https://www.ncbi.nlm.nih.gov/pubmed/35497022
http://dx.doi.org/10.1155/2022/5571542
_version_ 1784696334560788480
author Kakiuchi, Toshihiko
Matsuo, Muneaki
Sakata, Yasuhisa
Fujimoto, Kazuma
author_facet Kakiuchi, Toshihiko
Matsuo, Muneaki
Sakata, Yasuhisa
Fujimoto, Kazuma
author_sort Kakiuchi, Toshihiko
collection PubMed
description BACKGROUND: BLEIA ™ “EIKEN” Helicobacter pylori antigen (B[EIA]) is based on the bioluminescent enzyme immunoassay (BLEIA) method that was newly developed with high sensitivity in detecting Helicobacter pylori (H. pylori) antigen in feces. METHODS: In the project for H. pylori screening and treatment in Saga Prefecture in 2019, 141 students received the stool H. pylori antigen test as a secondary test. For 141 students, a comparative test was conducted between B (EIA) and extracorporeal diagnostic agents that were marketed in Japan as of 2019. The detection performance of H. pylori ATCC43504 standard strain and H. pylori antigen in commercial human fecal specimens were conducted. RESULTS: The comparison of B (EIA) with Quick Chaser (TM)H. pylori (Q [IC]) revealed positive and negative concordance ratios of B (EIA) to Q (IC) of 100.0% (110/110) and 71.0% (22/31), respectively. A comparative test was conducted between B (EIA) and extracorporeal diagnostic agents that were marketed in Japan as of 2019, and B (EIA) was most sensitive on “detecting H. pylori antigen of ATCC43504 standard strain” and “detecting H. pylori antigen in commercial human fecal specimens,” compared with other kits. Nine dissociated specimens that were negative for Q (IC) and positive for B (EIA) were confirmed. The measured value of B (EIA) in the dissociation samples were 1.3–87.4 cutoff index in the range that can be evaluated as negative by other fecal H. pylori antigen test kits, all the dissociation samples were H. pylori antigen-positive cases, and finally the cause of result divergence was presumed as false negative due to insufficient sensitivity of Q (IC). CONCLUSION: B (EIA) that is based on the BLEIA method, which applies firefly luciferase luminescence, is more sensitive than stool antigen test kits that are currently marketed in Japan and is very useful in diagnosing H. pylori infection, especially in situations where noninvasive tests are preferred, such as in children.
format Online
Article
Text
id pubmed-9050312
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-90503122022-04-29 Clinical Evaluation of a Novel Stool Antigen Test Using Bioluminescent Enzyme Immunoassay for Detecting Helicobacter pylori Kakiuchi, Toshihiko Matsuo, Muneaki Sakata, Yasuhisa Fujimoto, Kazuma Can J Gastroenterol Hepatol Research Article BACKGROUND: BLEIA ™ “EIKEN” Helicobacter pylori antigen (B[EIA]) is based on the bioluminescent enzyme immunoassay (BLEIA) method that was newly developed with high sensitivity in detecting Helicobacter pylori (H. pylori) antigen in feces. METHODS: In the project for H. pylori screening and treatment in Saga Prefecture in 2019, 141 students received the stool H. pylori antigen test as a secondary test. For 141 students, a comparative test was conducted between B (EIA) and extracorporeal diagnostic agents that were marketed in Japan as of 2019. The detection performance of H. pylori ATCC43504 standard strain and H. pylori antigen in commercial human fecal specimens were conducted. RESULTS: The comparison of B (EIA) with Quick Chaser (TM)H. pylori (Q [IC]) revealed positive and negative concordance ratios of B (EIA) to Q (IC) of 100.0% (110/110) and 71.0% (22/31), respectively. A comparative test was conducted between B (EIA) and extracorporeal diagnostic agents that were marketed in Japan as of 2019, and B (EIA) was most sensitive on “detecting H. pylori antigen of ATCC43504 standard strain” and “detecting H. pylori antigen in commercial human fecal specimens,” compared with other kits. Nine dissociated specimens that were negative for Q (IC) and positive for B (EIA) were confirmed. The measured value of B (EIA) in the dissociation samples were 1.3–87.4 cutoff index in the range that can be evaluated as negative by other fecal H. pylori antigen test kits, all the dissociation samples were H. pylori antigen-positive cases, and finally the cause of result divergence was presumed as false negative due to insufficient sensitivity of Q (IC). CONCLUSION: B (EIA) that is based on the BLEIA method, which applies firefly luciferase luminescence, is more sensitive than stool antigen test kits that are currently marketed in Japan and is very useful in diagnosing H. pylori infection, especially in situations where noninvasive tests are preferred, such as in children. Hindawi 2022-04-21 /pmc/articles/PMC9050312/ /pubmed/35497022 http://dx.doi.org/10.1155/2022/5571542 Text en Copyright © 2022 Toshihiko Kakiuchi et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kakiuchi, Toshihiko
Matsuo, Muneaki
Sakata, Yasuhisa
Fujimoto, Kazuma
Clinical Evaluation of a Novel Stool Antigen Test Using Bioluminescent Enzyme Immunoassay for Detecting Helicobacter pylori
title Clinical Evaluation of a Novel Stool Antigen Test Using Bioluminescent Enzyme Immunoassay for Detecting Helicobacter pylori
title_full Clinical Evaluation of a Novel Stool Antigen Test Using Bioluminescent Enzyme Immunoassay for Detecting Helicobacter pylori
title_fullStr Clinical Evaluation of a Novel Stool Antigen Test Using Bioluminescent Enzyme Immunoassay for Detecting Helicobacter pylori
title_full_unstemmed Clinical Evaluation of a Novel Stool Antigen Test Using Bioluminescent Enzyme Immunoassay for Detecting Helicobacter pylori
title_short Clinical Evaluation of a Novel Stool Antigen Test Using Bioluminescent Enzyme Immunoassay for Detecting Helicobacter pylori
title_sort clinical evaluation of a novel stool antigen test using bioluminescent enzyme immunoassay for detecting helicobacter pylori
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050312/
https://www.ncbi.nlm.nih.gov/pubmed/35497022
http://dx.doi.org/10.1155/2022/5571542
work_keys_str_mv AT kakiuchitoshihiko clinicalevaluationofanovelstoolantigentestusingbioluminescentenzymeimmunoassayfordetectinghelicobacterpylori
AT matsuomuneaki clinicalevaluationofanovelstoolantigentestusingbioluminescentenzymeimmunoassayfordetectinghelicobacterpylori
AT sakatayasuhisa clinicalevaluationofanovelstoolantigentestusingbioluminescentenzymeimmunoassayfordetectinghelicobacterpylori
AT fujimotokazuma clinicalevaluationofanovelstoolantigentestusingbioluminescentenzymeimmunoassayfordetectinghelicobacterpylori