Please use this identifier to cite or link to this item: 10.1016/j.medici.2014.05.001
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dc.contributor.authorLeja, Marcis-
dc.contributor.authorLapina, Sanita-
dc.contributor.authorPolaka, Inese-
dc.contributor.authorRudzite, Dace-
dc.contributor.authorVilkoite, Ilona-
dc.contributor.authorDaugule, Ilva-
dc.contributor.authorBelkovets, Anna-
dc.contributor.authorPimanov, Sergey-
dc.contributor.authorMakarenko, Jelena-
dc.contributor.authorTolmanis, Ivars-
dc.contributor.authorLejnieks, Aivars-
dc.contributor.authorBoka, Viesturs-
dc.contributor.authorRumba-Rozenfelde, Ingrida-
dc.contributor.authorVikmanis, Uldis-
dc.date.accessioned2021-05-31T09:55:01Z-
dc.date.available2021-05-31T09:55:01Z-
dc.date.issued2014-
dc.identifier.citationLeja , M , Lapina , S , Polaka , I , Rudzite , D , Vilkoite , I , Daugule , I , Belkovets , A , Pimanov , S , Makarenko , J , Tolmanis , I , Lejnieks , A , Boka , V , Rumba-Rozenfelde , I & Vikmanis , U 2014 , ' Pepsinogen testing for evaluation of the success of Helicobacter pylori eradication at 4 weeks after completion of therapy ' , Medicina (Lithuania) , vol. 50 , no. 1 , pp. 8-13 . https://doi.org/10.1016/j.medici.2014.05.001-
dc.identifier.issn1010-660X-
dc.identifier.urihttps://dspace.rsu.lv/jspui/handle/123456789/4581-
dc.descriptionFunding Information: This study was supported in part from the European Fund for Regional Development project No. 2010/0302/2DP/2.1.1.1.0/10/APIA/VIAA/158 entitled “Development of a Genetic/Serological Biomarker Diagnostic Method for Early Identification of Autoimmune Gastrointestinal Lesions With Increased Malignancy Risk in Patients With Autoimmune Disease.” Publisher Copyright: © 2014 Lithuanian University of Health Sciences. Production and hosting by Elsevier Urban & Partner Sp. z o.o. Copyright: Copyright 2017 Elsevier B.V., All rights reserved.-
dc.description.abstractBackground and objective: Pepsinogen levels in plasma are increased by inflammation in the gastric mucosa, including inflammation resulting from Helicobacter pylori infection. A decrease in pepsinogen II level has been suggested as a reliable marker to confirm the successful eradication of infection. The aim of our study was to evaluate the potential role of pepsinogens I and II, gastrin-17 and H. pylori antibodies in confirming successful eradication. Material and methods: Altogether 42 patients (25 women, 17 men), mean age 45 years (range 23-74), were enrolled. Pepsinogens I and II, gastrin-17 and H. pylori IgG antibodies were measured in plasma samples using an ELISA test (Biohit, Oyj., Finland) before the eradication and 4 weeks after completing the treatment. The success of eradication was determined by a urea breath test. Results: Eradication was successful in 31 patients (74%) and unsuccessful in 11 patients (26%). Pepsinogen II decreased significantly in both the successful (P = 0.029) and unsuccessful (P = 0.042) eradication groups. Pepsinogen I decreased significantly in the successful (P = 0.025) but not the unsuccessful (P = 0.29) eradication group. The pepsinogen I/II ratio increased in the successful eradication group (P = 0.0018) but not in the group in which treatment failed (P = 0.12). There were no differences in gastrin-17 or H. pylori antibody values. Conclusions: A decrease in pepsinogen II levels cannot be used as a reliable marker for the successful eradication of H. pylori 4 weeks after the completion of treatment. The increase in pepsinogen I/II ratio reflects differences in pepsinogen production following the eradication irrespective of improvement in atrophy.en
dc.format.extent6-
dc.format.extent706109-
dc.language.isoeng-
dc.relation.ispartofMedicina (Lithuania)-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.subjectEfficacy-
dc.subjectEradication-
dc.subjectGastrin-17-
dc.subjectHelicobacter pylori-
dc.subjectPepsinogen-
dc.subject3.2 Clinical medicine-
dc.subject1.1. Scientific article indexed in Web of Science and/or Scopus database-
dc.subjectGeneral Medicine-
dc.titlePepsinogen testing for evaluation of the success of Helicobacter pylori eradication at 4 weeks after completion of therapyen
dc.type/dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article-
dc.identifier.doi10.1016/j.medici.2014.05.001-
dc.contributor.institutionRīga Stradiņš University-
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=84906965400&partnerID=8YFLogxK-
dc.description.statusPeer reviewed-
Appears in Collections:Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure

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