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Multiple cytokine profiling in serum for early detection of gastric cancer

AIM: To investigate the value of multiparameter joint analysis in the early diagnosis of gastric cancer (GC) in clinical practice. METHODS: Concentrations of CEA, CA724 and three kinds of cytokines (TNF-α, IL-6 and IL-8) in 176 GC patients, 117 atypical hyperplasia patients, and 204 healthy control...

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Autores principales: Li, Jian, Xu, Liang, Run, Zeng-Ci, Feng, Wen, Liu, Wen, Zhang, Peng-Jun, Li, Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989241/
https://www.ncbi.nlm.nih.gov/pubmed/29881236
http://dx.doi.org/10.3748/wjg.v24.i21.2269
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author Li, Jian
Xu, Liang
Run, Zeng-Ci
Feng, Wen
Liu, Wen
Zhang, Peng-Jun
Li, Zhi
author_facet Li, Jian
Xu, Liang
Run, Zeng-Ci
Feng, Wen
Liu, Wen
Zhang, Peng-Jun
Li, Zhi
author_sort Li, Jian
collection PubMed
description AIM: To investigate the value of multiparameter joint analysis in the early diagnosis of gastric cancer (GC) in clinical practice. METHODS: Concentrations of CEA, CA724 and three kinds of cytokines (TNF-α, IL-6 and IL-8) in 176 GC patients, 117 atypical hyperplasia patients, and 204 healthy control individuals were used for building the diagnostic model, then 58 GC patients, 41 atypical hyperplasia patients, and 66 healthy control individuals were enrolled independently. The joints of the indicators were analyzed by binary logistic regression analysis method. RESULTS: For discriminating the healthy control group and the GC group, IL-6 had the best diagnostic value, and the area under curve (AUC) of joint analysis was 0.95 (0.93-0.97). For the early stage and advanced stage GC, the AUC were 0.95 (0.92-0.98) and 0.95 (0.92-0.97). For discriminating the atypical hyperplasia group and GC group, CA724 had the best diagnostic value, and the AUC of joint analysis was 0.97 (0.95-0.99). For the early stage and advanced stage GC groups, the AUC were 0.98 (0.96-0.99) and 0.96 (0.94-0.98). After evaluation, for discriminating the GC, early stage GC and advanced cancer group from the healthy control group, the diagnostic sensitivity was 89.66%, 84.21% and 92.31%, respectively, and the specificity was 92.42%, 90.91% and 90.91%. For discriminating the GC, early stage GC and advanced cancer groups from the atypical hyperplasia group, the diagnostic sensitivity was 87.93%, 78.95% and 92.31%, respectively, and the specificity was 87.80%, 85.37% and 90.24%. CONCLUSION: We have built a diagnostic model including CEA, CA724, IL-6, IL-8, and TNF-α. It may provide potential assistance as a screening method for the early detection of GC.
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spelling pubmed-59892412018-06-08 Multiple cytokine profiling in serum for early detection of gastric cancer Li, Jian Xu, Liang Run, Zeng-Ci Feng, Wen Liu, Wen Zhang, Peng-Jun Li, Zhi World J Gastroenterol Basic Study AIM: To investigate the value of multiparameter joint analysis in the early diagnosis of gastric cancer (GC) in clinical practice. METHODS: Concentrations of CEA, CA724 and three kinds of cytokines (TNF-α, IL-6 and IL-8) in 176 GC patients, 117 atypical hyperplasia patients, and 204 healthy control individuals were used for building the diagnostic model, then 58 GC patients, 41 atypical hyperplasia patients, and 66 healthy control individuals were enrolled independently. The joints of the indicators were analyzed by binary logistic regression analysis method. RESULTS: For discriminating the healthy control group and the GC group, IL-6 had the best diagnostic value, and the area under curve (AUC) of joint analysis was 0.95 (0.93-0.97). For the early stage and advanced stage GC, the AUC were 0.95 (0.92-0.98) and 0.95 (0.92-0.97). For discriminating the atypical hyperplasia group and GC group, CA724 had the best diagnostic value, and the AUC of joint analysis was 0.97 (0.95-0.99). For the early stage and advanced stage GC groups, the AUC were 0.98 (0.96-0.99) and 0.96 (0.94-0.98). After evaluation, for discriminating the GC, early stage GC and advanced cancer group from the healthy control group, the diagnostic sensitivity was 89.66%, 84.21% and 92.31%, respectively, and the specificity was 92.42%, 90.91% and 90.91%. For discriminating the GC, early stage GC and advanced cancer groups from the atypical hyperplasia group, the diagnostic sensitivity was 87.93%, 78.95% and 92.31%, respectively, and the specificity was 87.80%, 85.37% and 90.24%. CONCLUSION: We have built a diagnostic model including CEA, CA724, IL-6, IL-8, and TNF-α. It may provide potential assistance as a screening method for the early detection of GC. Baishideng Publishing Group Inc 2018-06-07 2018-06-07 /pmc/articles/PMC5989241/ /pubmed/29881236 http://dx.doi.org/10.3748/wjg.v24.i21.2269 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Basic Study
Li, Jian
Xu, Liang
Run, Zeng-Ci
Feng, Wen
Liu, Wen
Zhang, Peng-Jun
Li, Zhi
Multiple cytokine profiling in serum for early detection of gastric cancer
title Multiple cytokine profiling in serum for early detection of gastric cancer
title_full Multiple cytokine profiling in serum for early detection of gastric cancer
title_fullStr Multiple cytokine profiling in serum for early detection of gastric cancer
title_full_unstemmed Multiple cytokine profiling in serum for early detection of gastric cancer
title_short Multiple cytokine profiling in serum for early detection of gastric cancer
title_sort multiple cytokine profiling in serum for early detection of gastric cancer
topic Basic Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989241/
https://www.ncbi.nlm.nih.gov/pubmed/29881236
http://dx.doi.org/10.3748/wjg.v24.i21.2269
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