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Newer agents for Helicobacter pylori eradication
Helicobacter pylori infection remains widespread internationally, with a definite morbidity and mortality. The efficacy of standard 7–14 day triple therapies is decreasing, mainly due to increasing primary bacterial resistance to antibiotics. Currently, the most effective treatments are either the s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387829/ https://www.ncbi.nlm.nih.gov/pubmed/22767998 http://dx.doi.org/10.2147/CEG.S25422 |
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author | Fiorini, Giulia Zullo, Angelo Gatta, Luigi Castelli, Valentina Ricci, Chiara Cassol, Francesca Vaira, Dino |
author_facet | Fiorini, Giulia Zullo, Angelo Gatta, Luigi Castelli, Valentina Ricci, Chiara Cassol, Francesca Vaira, Dino |
author_sort | Fiorini, Giulia |
collection | PubMed |
description | Helicobacter pylori infection remains widespread internationally, with a definite morbidity and mortality. The efficacy of standard 7–14 day triple therapies is decreasing, mainly due to increasing primary bacterial resistance to antibiotics. Currently, the most effective treatments are either the sequential regimen or the concomitant therapy. Different patents have been registered showing high bactericidal effects in vitro, some of which are active against clarithromycin- and metronidazole-resistant strains, even at low pH values. Among these novel molecules, benzimidazole-derivatives, polycyclic compounds, pyloricidin, and arylthiazole analogues seem to be the more promising. The identification of essential genes for either bacterial colonization or growth represents a route for potential target therapies in the near future. |
format | Online Article Text |
id | pubmed-3387829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33878292012-07-05 Newer agents for Helicobacter pylori eradication Fiorini, Giulia Zullo, Angelo Gatta, Luigi Castelli, Valentina Ricci, Chiara Cassol, Francesca Vaira, Dino Clin Exp Gastroenterol Review Helicobacter pylori infection remains widespread internationally, with a definite morbidity and mortality. The efficacy of standard 7–14 day triple therapies is decreasing, mainly due to increasing primary bacterial resistance to antibiotics. Currently, the most effective treatments are either the sequential regimen or the concomitant therapy. Different patents have been registered showing high bactericidal effects in vitro, some of which are active against clarithromycin- and metronidazole-resistant strains, even at low pH values. Among these novel molecules, benzimidazole-derivatives, polycyclic compounds, pyloricidin, and arylthiazole analogues seem to be the more promising. The identification of essential genes for either bacterial colonization or growth represents a route for potential target therapies in the near future. Dove Medical Press 2012-06-18 /pmc/articles/PMC3387829/ /pubmed/22767998 http://dx.doi.org/10.2147/CEG.S25422 Text en © 2012 Fiorini et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Review Fiorini, Giulia Zullo, Angelo Gatta, Luigi Castelli, Valentina Ricci, Chiara Cassol, Francesca Vaira, Dino Newer agents for Helicobacter pylori eradication |
title | Newer agents for Helicobacter pylori eradication |
title_full | Newer agents for Helicobacter pylori eradication |
title_fullStr | Newer agents for Helicobacter pylori eradication |
title_full_unstemmed | Newer agents for Helicobacter pylori eradication |
title_short | Newer agents for Helicobacter pylori eradication |
title_sort | newer agents for helicobacter pylori eradication |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387829/ https://www.ncbi.nlm.nih.gov/pubmed/22767998 http://dx.doi.org/10.2147/CEG.S25422 |
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