Expression of M30 and M65 in celiac disease. Analytical cross-sectional study
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | São Paulo medical journal (Online) |
Texto Completo: | https://periodicosapm.emnuvens.com.br/spmj/article/view/616 |
Resumo: | BACKGROUND: The role of villous atrophy in apoptosis, a distinctive feature of celiac disease, is a matter of controversy. The aim of this study was to determine the apoptosis rate through immunohistochemical staining for M30 and M65 in celiac disease cases. DESIGN AND SETTING: Analytical cross-sectional study in a tertiary-level center. METHODS: Duodenal biopsies from 28 treatment-naive patients with celiac disease, 16 patients with po- tential celiac disease, 10 patients with a gluten-free diet and 8 controls were subjected to immunohisto- chemical staining for the end-apoptotic marker M30 and the total cell death marker M65. H-scores were compared. Several laboratory parameters were recorded concomitantly, and at the one-year follow-up for celiac disease and potential celiac disease patients. RESULTS: There was a significant difference in H-score for M30 expression between the celiac disease, potential celiac disease and gluten-free diet groups (P = 0.009). There was no significant difference in H-score for M65 expression. There was a positive correlation between the H-score for M30 expression and the anti-tissue transglutaminase immunoglobulin A (anti-tTgIgA) and anti-tissue transglutaminase immunoglobulin G (anti-tTgIgG) levels (R = 0.285, P = 0.036; and R = 0.307, P = 0.024, respectively); and between the H-score for M65 expression and the anti-tTgIgA and anti-tTgIgG levels (R = 0.265, P = 0.053; and R = 0.314, P = 0.021, respectively). There was no difference between celiac disease and potential celiac disease patients regarding the laboratory parameters selected. CONCLUSION: The rates of apoptosis and nutritional deficiencies in patients with potential celiac disease were similar to those in patients with celiac disease. |
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Expression of M30 and M65 in celiac disease. Analytical cross-sectional studyCeliac diseaseM30 cytokeratin-18 peptide, humanM65 antigen, humanBACKGROUND: The role of villous atrophy in apoptosis, a distinctive feature of celiac disease, is a matter of controversy. The aim of this study was to determine the apoptosis rate through immunohistochemical staining for M30 and M65 in celiac disease cases. DESIGN AND SETTING: Analytical cross-sectional study in a tertiary-level center. METHODS: Duodenal biopsies from 28 treatment-naive patients with celiac disease, 16 patients with po- tential celiac disease, 10 patients with a gluten-free diet and 8 controls were subjected to immunohisto- chemical staining for the end-apoptotic marker M30 and the total cell death marker M65. H-scores were compared. Several laboratory parameters were recorded concomitantly, and at the one-year follow-up for celiac disease and potential celiac disease patients. RESULTS: There was a significant difference in H-score for M30 expression between the celiac disease, potential celiac disease and gluten-free diet groups (P = 0.009). There was no significant difference in H-score for M65 expression. There was a positive correlation between the H-score for M30 expression and the anti-tissue transglutaminase immunoglobulin A (anti-tTgIgA) and anti-tissue transglutaminase immunoglobulin G (anti-tTgIgG) levels (R = 0.285, P = 0.036; and R = 0.307, P = 0.024, respectively); and between the H-score for M65 expression and the anti-tTgIgA and anti-tTgIgG levels (R = 0.265, P = 0.053; and R = 0.314, P = 0.021, respectively). There was no difference between celiac disease and potential celiac disease patients regarding the laboratory parameters selected. CONCLUSION: The rates of apoptosis and nutritional deficiencies in patients with potential celiac disease were similar to those in patients with celiac disease.São Paulo Medical JournalSão Paulo Medical Journal2018-12-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://periodicosapm.emnuvens.com.br/spmj/article/view/616São Paulo Medical Journal; Vol. 136 No. 6 (2018); 525-532São Paulo Medical Journal; v. 136 n. 6 (2018); 525-5321806-9460reponame:São Paulo medical journal (Online)instname:Associação Paulista de Medicinainstacron:APMenghttps://periodicosapm.emnuvens.com.br/spmj/article/view/616/559https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessAksoy, Evrim KahramanoğluŞimşek, Gülçin GülerTorgutalp, MuratSapmaz, Ferdane PirinççiAkpınar, Muhammet YenerUzman, MetinNazlıgül, Yaşar2023-08-31T21:42:33Zoai:ojs.diagnosticoetratamento.emnuvens.com.br:article/616Revistahttp://www.scielo.br/spmjPUBhttps://old.scielo.br/oai/scielo-oai.phprevistas@apm.org.br1806-94601516-3180opendoar:2023-08-31T21:42:33São Paulo medical journal (Online) - Associação Paulista de Medicinafalse |
dc.title.none.fl_str_mv |
Expression of M30 and M65 in celiac disease. Analytical cross-sectional study |
title |
Expression of M30 and M65 in celiac disease. Analytical cross-sectional study |
spellingShingle |
Expression of M30 and M65 in celiac disease. Analytical cross-sectional study Aksoy, Evrim Kahramanoğlu Celiac disease M30 cytokeratin-18 peptide, human M65 antigen, human |
title_short |
Expression of M30 and M65 in celiac disease. Analytical cross-sectional study |
title_full |
Expression of M30 and M65 in celiac disease. Analytical cross-sectional study |
title_fullStr |
Expression of M30 and M65 in celiac disease. Analytical cross-sectional study |
title_full_unstemmed |
Expression of M30 and M65 in celiac disease. Analytical cross-sectional study |
title_sort |
Expression of M30 and M65 in celiac disease. Analytical cross-sectional study |
author |
Aksoy, Evrim Kahramanoğlu |
author_facet |
Aksoy, Evrim Kahramanoğlu Şimşek, Gülçin Güler Torgutalp, Murat Sapmaz, Ferdane Pirinççi Akpınar, Muhammet Yener Uzman, Metin Nazlıgül, Yaşar |
author_role |
author |
author2 |
Şimşek, Gülçin Güler Torgutalp, Murat Sapmaz, Ferdane Pirinççi Akpınar, Muhammet Yener Uzman, Metin Nazlıgül, Yaşar |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Aksoy, Evrim Kahramanoğlu Şimşek, Gülçin Güler Torgutalp, Murat Sapmaz, Ferdane Pirinççi Akpınar, Muhammet Yener Uzman, Metin Nazlıgül, Yaşar |
dc.subject.por.fl_str_mv |
Celiac disease M30 cytokeratin-18 peptide, human M65 antigen, human |
topic |
Celiac disease M30 cytokeratin-18 peptide, human M65 antigen, human |
description |
BACKGROUND: The role of villous atrophy in apoptosis, a distinctive feature of celiac disease, is a matter of controversy. The aim of this study was to determine the apoptosis rate through immunohistochemical staining for M30 and M65 in celiac disease cases. DESIGN AND SETTING: Analytical cross-sectional study in a tertiary-level center. METHODS: Duodenal biopsies from 28 treatment-naive patients with celiac disease, 16 patients with po- tential celiac disease, 10 patients with a gluten-free diet and 8 controls were subjected to immunohisto- chemical staining for the end-apoptotic marker M30 and the total cell death marker M65. H-scores were compared. Several laboratory parameters were recorded concomitantly, and at the one-year follow-up for celiac disease and potential celiac disease patients. RESULTS: There was a significant difference in H-score for M30 expression between the celiac disease, potential celiac disease and gluten-free diet groups (P = 0.009). There was no significant difference in H-score for M65 expression. There was a positive correlation between the H-score for M30 expression and the anti-tissue transglutaminase immunoglobulin A (anti-tTgIgA) and anti-tissue transglutaminase immunoglobulin G (anti-tTgIgG) levels (R = 0.285, P = 0.036; and R = 0.307, P = 0.024, respectively); and between the H-score for M65 expression and the anti-tTgIgA and anti-tTgIgG levels (R = 0.265, P = 0.053; and R = 0.314, P = 0.021, respectively). There was no difference between celiac disease and potential celiac disease patients regarding the laboratory parameters selected. CONCLUSION: The rates of apoptosis and nutritional deficiencies in patients with potential celiac disease were similar to those in patients with celiac disease. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-06 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://periodicosapm.emnuvens.com.br/spmj/article/view/616 |
url |
https://periodicosapm.emnuvens.com.br/spmj/article/view/616 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://periodicosapm.emnuvens.com.br/spmj/article/view/616/559 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
São Paulo Medical Journal São Paulo Medical Journal |
publisher.none.fl_str_mv |
São Paulo Medical Journal São Paulo Medical Journal |
dc.source.none.fl_str_mv |
São Paulo Medical Journal; Vol. 136 No. 6 (2018); 525-532 São Paulo Medical Journal; v. 136 n. 6 (2018); 525-532 1806-9460 reponame:São Paulo medical journal (Online) instname:Associação Paulista de Medicina instacron:APM |
instname_str |
Associação Paulista de Medicina |
instacron_str |
APM |
institution |
APM |
reponame_str |
São Paulo medical journal (Online) |
collection |
São Paulo medical journal (Online) |
repository.name.fl_str_mv |
São Paulo medical journal (Online) - Associação Paulista de Medicina |
repository.mail.fl_str_mv |
revistas@apm.org.br |
_version_ |
1825135057567744000 |