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The serum pepsinogen levels for risk assessment of gastric neoplasms New proposal from a case-control study in Korea

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dc.contributor.authorCho, Jun-Hyung-
dc.contributor.authorJeon, Seong Ran-
dc.contributor.authorKim, Hyun Gun-
dc.contributor.authorJin, So-Young-
dc.contributor.authorPark, Suyeon-
dc.date.accessioned2021-08-11T14:43:58Z-
dc.date.available2021-08-11T14:43:58Z-
dc.date.issued2017-07-
dc.identifier.issn0025-7974-
dc.identifier.issn1536-5964-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/7397-
dc.description.abstractTo decrease the gastric cancer related mortality rate, endoscopic screening is widely performed in Korea. However, a precise method for identifying those at a high risk of gastric neoplasms has not been established. This study aims to evaluate serum pepsinogen (PG) levels for risk assessment of gastric neoplasms. Between August 2014 and March 2016, a total of 398 subjects, including 87 with gastric neoplasms, were enrolled in this study. On the basis of the serum PG I/II ratio, the enrolled subjects were classified into 4 groups: group A, PG I/II ratio > 4; group B, > 3 and <= 4; group C, > 2 and <= 3; group D, <= 2. Compared with group A, a stepwise increase in the risk of gastric neoplasm was observed from group B [ odds ratio (OR) = 9.9, 95% confidence interval (95% CI) = 4.0-24.4] to group C (OR = 20.9, 95% CI = 8.7-50.5) to group D (OR = 37.3, 95% CI = 14.3-97.4). The optimal cutoff value of the serum PG I/II ratio for predicting gastric neoplasms was 4.5, with a sensitivity of 97.7% and a specificity of 57.6%. A decrease in the serum PG I/II ratio was strongly associated with an increased risk of gastric neoplasms. The serum PG I/II ratio can be used to identify those at a high risk of gastric neoplasms in Korean population.-
dc.language영어-
dc.language.isoENG-
dc.publisherLippincott Williams & Wilkins Ltd.-
dc.titleThe serum pepsinogen levels for risk assessment of gastric neoplasms New proposal from a case-control study in Korea-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1097/MD.0000000000007603-
dc.identifier.scopusid2-s2.0-85026416221-
dc.identifier.wosid000406477600071-
dc.identifier.bibliographicCitationMedicine, v.96, no.29-
dc.citation.titleMedicine-
dc.citation.volume96-
dc.citation.number29-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.subject.keywordPlusHELICOBACTER-PYLORI INFECTION-
dc.subject.keywordPlusCANCER SCREENING-PROGRAM-
dc.subject.keywordPlusATROPHIC GASTRITIS-
dc.subject.keywordPlusANTIBODY-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordPlusMUCOSA-
dc.subject.keywordPlusSURVEILLANCE-
dc.subject.keywordPlusPREVALENCE-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusENDOSCOPY-
dc.subject.keywordAuthoratrophy-
dc.subject.keywordAuthorgastric neoplasm-
dc.subject.keywordAuthorHelicobacter pylori-
dc.subject.keywordAuthorpepsinogen-
dc.subject.keywordAuthorrisk-
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