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Link between Serum Pepsinogen Concentrations and Upper Gastrointestinal Endoscopic Findings

The serum pepsinogen (PG) assay findings are correlated with the status of Helicobacter pylori infection, but there are controversies on the link with upper gastrointestinal (UGI) endoscopic findings. The aim of this study was to determine the significance of a serum PG assay for correlating with en...

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Autores principales: Lee, Sang Pyo, Lee, Sun-Young, Kim, Jeong Hwan, Sung, In-Kyung, Park, Hyung Seok, Shim, Chan Sup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383612/
https://www.ncbi.nlm.nih.gov/pubmed/28378553
http://dx.doi.org/10.3346/jkms.2017.32.5.796
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author Lee, Sang Pyo
Lee, Sun-Young
Kim, Jeong Hwan
Sung, In-Kyung
Park, Hyung Seok
Shim, Chan Sup
author_facet Lee, Sang Pyo
Lee, Sun-Young
Kim, Jeong Hwan
Sung, In-Kyung
Park, Hyung Seok
Shim, Chan Sup
author_sort Lee, Sang Pyo
collection PubMed
description The serum pepsinogen (PG) assay findings are correlated with the status of Helicobacter pylori infection, but there are controversies on the link with upper gastrointestinal (UGI) endoscopic findings. The aim of this study was to determine the significance of a serum PG assay for correlating with endoscopic findings in H. pylori-seroprevalent adult population. Korean adults who visited for a health check-up were included consecutively. Subjects after gastrectomy or H. pylori eradication were excluded. After completing the serum PG assay and anti-H. pylori immunoglobulin G (IgG) titer on the same day of UGI endoscopy, subjects with equivocal serology test finding or gastric neoplasm were excluded. Of the 4,830 included subjects, 3,116 (64.5%) were seropositive for H. pylori. Seropositive finding was related to high serum PG I (P < 0.001) and PG II (P < 0.001) concentrations, low PG I/II ratio (P < 0.001), old age (P < 0.001), and male gender (P = 0.006). After adjusting age and gender, the serum PG I and II concentrations were positively correlated with the presence of nodular gastritis (NG) (all P = 0.003). The serum PG I was positively correlated with gastric ulcer (P = 0.003), and it was correlated with duodenal ulcer in seropositive subjects (P = 0.008). The PG I/II ratio was positively correlated with erosive esophagitis, while it was inversely related to chronic atrophic gastritis and metaplastic gastritis (all P < 0.001). Our findings suggest that the serum PG assay finding correlates well with the UGI endoscopic finding. A higher serum PG concentration in subjects with NG and peptic ulcer disease suggests that endoscopic findings reflect gastric secreting ability.
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spelling pubmed-53836122017-05-01 Link between Serum Pepsinogen Concentrations and Upper Gastrointestinal Endoscopic Findings Lee, Sang Pyo Lee, Sun-Young Kim, Jeong Hwan Sung, In-Kyung Park, Hyung Seok Shim, Chan Sup J Korean Med Sci Original Article The serum pepsinogen (PG) assay findings are correlated with the status of Helicobacter pylori infection, but there are controversies on the link with upper gastrointestinal (UGI) endoscopic findings. The aim of this study was to determine the significance of a serum PG assay for correlating with endoscopic findings in H. pylori-seroprevalent adult population. Korean adults who visited for a health check-up were included consecutively. Subjects after gastrectomy or H. pylori eradication were excluded. After completing the serum PG assay and anti-H. pylori immunoglobulin G (IgG) titer on the same day of UGI endoscopy, subjects with equivocal serology test finding or gastric neoplasm were excluded. Of the 4,830 included subjects, 3,116 (64.5%) were seropositive for H. pylori. Seropositive finding was related to high serum PG I (P < 0.001) and PG II (P < 0.001) concentrations, low PG I/II ratio (P < 0.001), old age (P < 0.001), and male gender (P = 0.006). After adjusting age and gender, the serum PG I and II concentrations were positively correlated with the presence of nodular gastritis (NG) (all P = 0.003). The serum PG I was positively correlated with gastric ulcer (P = 0.003), and it was correlated with duodenal ulcer in seropositive subjects (P = 0.008). The PG I/II ratio was positively correlated with erosive esophagitis, while it was inversely related to chronic atrophic gastritis and metaplastic gastritis (all P < 0.001). Our findings suggest that the serum PG assay finding correlates well with the UGI endoscopic finding. A higher serum PG concentration in subjects with NG and peptic ulcer disease suggests that endoscopic findings reflect gastric secreting ability. The Korean Academy of Medical Sciences 2017-05 2017-03-07 /pmc/articles/PMC5383612/ /pubmed/28378553 http://dx.doi.org/10.3346/jkms.2017.32.5.796 Text en © 2017 The Korean Academy of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Sang Pyo
Lee, Sun-Young
Kim, Jeong Hwan
Sung, In-Kyung
Park, Hyung Seok
Shim, Chan Sup
Link between Serum Pepsinogen Concentrations and Upper Gastrointestinal Endoscopic Findings
title Link between Serum Pepsinogen Concentrations and Upper Gastrointestinal Endoscopic Findings
title_full Link between Serum Pepsinogen Concentrations and Upper Gastrointestinal Endoscopic Findings
title_fullStr Link between Serum Pepsinogen Concentrations and Upper Gastrointestinal Endoscopic Findings
title_full_unstemmed Link between Serum Pepsinogen Concentrations and Upper Gastrointestinal Endoscopic Findings
title_short Link between Serum Pepsinogen Concentrations and Upper Gastrointestinal Endoscopic Findings
title_sort link between serum pepsinogen concentrations and upper gastrointestinal endoscopic findings
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383612/
https://www.ncbi.nlm.nih.gov/pubmed/28378553
http://dx.doi.org/10.3346/jkms.2017.32.5.796
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