Interleukin 8 (-251 T>A) polymorphism in children and teenagers infected with Helicobacter pylori

Detalhes bibliográficos
Autor(a) principal: Saes,Marina
Data de Publicação: 2017
Outros Autores: Labio,Roger Willian de, Rasmussen,Lucas Trevizani, Payão,Spencer Luiz Marques
Tipo de documento: Artigo
Idioma: eng
Título da fonte: The Journal of venomous animals and toxins including tropical diseases (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992017000100601
Resumo: Abstract Background Helicobacter pylori (H. pylori) is a gram-negative bacterium that colonizes the human stomach and causes a variety of gastric diseases. This study evaluated the correlations between the -251 (T>A) (rs4073) polymorphism of interleukin-8 (IL-8), the etiology of gastric disease, and H. pylori infection in pediatric and adolescent patients. Methods DNA samples were obtained from 285 gastric biopsies from pediatric patients. H. pylori was detected by PCR, whereas PCR-RFLP was used to characterize the -251 (T>A) polymorphism of IL-8. Results The histological analysis revealed the presence of gastritis in 158 patients (55.44%). H. pylori was found in 71 samples (24.9%). The -251 (T>A) polymorphism revealed that 58 (29.47%) samples were TT, 143 (50.18%) samples were TA, and 84 (20.35%) samples were AA. Conclusions Our findings suggest that IL8-251 A allele may be an important risk factor for the development of gastric disease when associated with H. pylori infection.
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spelling Interleukin 8 (-251 T>A) polymorphism in children and teenagers infected with Helicobacter pyloriHelicobacter pyloriInterleukin 8Polymorphism-251 (T>A)Gastric diseaseAbstract Background Helicobacter pylori (H. pylori) is a gram-negative bacterium that colonizes the human stomach and causes a variety of gastric diseases. This study evaluated the correlations between the -251 (T>A) (rs4073) polymorphism of interleukin-8 (IL-8), the etiology of gastric disease, and H. pylori infection in pediatric and adolescent patients. Methods DNA samples were obtained from 285 gastric biopsies from pediatric patients. H. pylori was detected by PCR, whereas PCR-RFLP was used to characterize the -251 (T>A) polymorphism of IL-8. Results The histological analysis revealed the presence of gastritis in 158 patients (55.44%). H. pylori was found in 71 samples (24.9%). The -251 (T>A) polymorphism revealed that 58 (29.47%) samples were TT, 143 (50.18%) samples were TA, and 84 (20.35%) samples were AA. Conclusions Our findings suggest that IL8-251 A allele may be an important risk factor for the development of gastric disease when associated with H. pylori infection.Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP)2017-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992017000100601Journal of Venomous Animals and Toxins including Tropical Diseases v.23 2017reponame:The Journal of venomous animals and toxins including tropical diseases (Online)instname:Universidade Estadual Paulista (UNESP)instacron:UNESP10.1186/s40409-017-0113-zinfo:eu-repo/semantics/openAccessSaes,MarinaLabio,Roger Willian deRasmussen,Lucas TrevizaniPayão,Spencer Luiz Marqueseng2017-07-03T00:00:00Zoai:scielo:S1678-91992017000100601Revistahttp://www.scielo.br/jvatitdPUBhttps://old.scielo.br/oai/scielo-oai.php||editorial@jvat.org.br1678-91991678-9180opendoar:2017-07-03T00:00The Journal of venomous animals and toxins including tropical diseases (Online) - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Interleukin 8 (-251 T>A) polymorphism in children and teenagers infected with Helicobacter pylori
title Interleukin 8 (-251 T>A) polymorphism in children and teenagers infected with Helicobacter pylori
spellingShingle Interleukin 8 (-251 T>A) polymorphism in children and teenagers infected with Helicobacter pylori
Saes,Marina
Helicobacter pylori
Interleukin 8
Polymorphism
-251 (T>A)
Gastric disease
title_short Interleukin 8 (-251 T>A) polymorphism in children and teenagers infected with Helicobacter pylori
title_full Interleukin 8 (-251 T>A) polymorphism in children and teenagers infected with Helicobacter pylori
title_fullStr Interleukin 8 (-251 T>A) polymorphism in children and teenagers infected with Helicobacter pylori
title_full_unstemmed Interleukin 8 (-251 T>A) polymorphism in children and teenagers infected with Helicobacter pylori
title_sort Interleukin 8 (-251 T>A) polymorphism in children and teenagers infected with Helicobacter pylori
author Saes,Marina
author_facet Saes,Marina
Labio,Roger Willian de
Rasmussen,Lucas Trevizani
Payão,Spencer Luiz Marques
author_role author
author2 Labio,Roger Willian de
Rasmussen,Lucas Trevizani
Payão,Spencer Luiz Marques
author2_role author
author
author
dc.contributor.author.fl_str_mv Saes,Marina
Labio,Roger Willian de
Rasmussen,Lucas Trevizani
Payão,Spencer Luiz Marques
dc.subject.por.fl_str_mv Helicobacter pylori
Interleukin 8
Polymorphism
-251 (T>A)
Gastric disease
topic Helicobacter pylori
Interleukin 8
Polymorphism
-251 (T>A)
Gastric disease
description Abstract Background Helicobacter pylori (H. pylori) is a gram-negative bacterium that colonizes the human stomach and causes a variety of gastric diseases. This study evaluated the correlations between the -251 (T>A) (rs4073) polymorphism of interleukin-8 (IL-8), the etiology of gastric disease, and H. pylori infection in pediatric and adolescent patients. Methods DNA samples were obtained from 285 gastric biopsies from pediatric patients. H. pylori was detected by PCR, whereas PCR-RFLP was used to characterize the -251 (T>A) polymorphism of IL-8. Results The histological analysis revealed the presence of gastritis in 158 patients (55.44%). H. pylori was found in 71 samples (24.9%). The -251 (T>A) polymorphism revealed that 58 (29.47%) samples were TT, 143 (50.18%) samples were TA, and 84 (20.35%) samples were AA. Conclusions Our findings suggest that IL8-251 A allele may be an important risk factor for the development of gastric disease when associated with H. pylori infection.
publishDate 2017
dc.date.none.fl_str_mv 2017-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992017000100601
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992017000100601
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1186/s40409-017-0113-z
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP)
publisher.none.fl_str_mv Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP)
dc.source.none.fl_str_mv Journal of Venomous Animals and Toxins including Tropical Diseases v.23 2017
reponame:The Journal of venomous animals and toxins including tropical diseases (Online)
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str The Journal of venomous animals and toxins including tropical diseases (Online)
collection The Journal of venomous animals and toxins including tropical diseases (Online)
repository.name.fl_str_mv The Journal of venomous animals and toxins including tropical diseases (Online) - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv ||editorial@jvat.org.br
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