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Annexin A2 as a biomarker for hepatocellular carcinoma in Egyptian patients

AIM: To investigate the clinical utility of serum annexin A2 (ANXA2) as a diagnostic marker for early hepatocellular carcinoma (HCC). METHODS: This study was performed in HCC Clinic of Ain Shams University Hospitals, Cairo, Egypt and included: Group 1: Fifty patients with early stage HCC (Barcelona...

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Autores principales: Shaker, Mohamed K, Abdel Fattah, Hanzada I, Sabbour, Ghada S, Montasser, Iman F, Abdelhakam, Sara M, El Hadidy, Eman, Yousry, Rehab, El Dorry, Ahmed K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368624/
https://www.ncbi.nlm.nih.gov/pubmed/28396717
http://dx.doi.org/10.4254/wjh.v9.i9.469
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author Shaker, Mohamed K
Abdel Fattah, Hanzada I
Sabbour, Ghada S
Montasser, Iman F
Abdelhakam, Sara M
El Hadidy, Eman
Yousry, Rehab
El Dorry, Ahmed K
author_facet Shaker, Mohamed K
Abdel Fattah, Hanzada I
Sabbour, Ghada S
Montasser, Iman F
Abdelhakam, Sara M
El Hadidy, Eman
Yousry, Rehab
El Dorry, Ahmed K
author_sort Shaker, Mohamed K
collection PubMed
description AIM: To investigate the clinical utility of serum annexin A2 (ANXA2) as a diagnostic marker for early hepatocellular carcinoma (HCC). METHODS: This study was performed in HCC Clinic of Ain Shams University Hospitals, Cairo, Egypt and included: Group 1: Fifty patients with early stage HCC (Barcelona Clinic Liver Cancer stage A); Group 2: Twenty five patients with chronic liver disease; and Control Group: Fifteen healthy, age- and sex-matched subjects who were seronegative for viral hepatitis markers. The following laboratory investigations were done: Viral hepatitis markers [hepatitis B surface antigen and hepatitis C virus (HCV) antibodies], HCV RNA in HCV antibody-positive patients, serum alpha fetoprotein (AFP), and serum ANXA2 levels. RESULTS: In this study, 88% of HCC patients (n = 44) were HCV-positive, while HBV infection represented only 8% of all HCC patients (n = 4); and two patients were negative for both viral markers. A highly significant difference was found between patients with HCC and chronic liver disease as well as controls with regard to serum ANXA2 levels (130, IQR 15-240; 15, IQR 15-17; and 17, IQR 15-30 ng/mL, respectively). The area under the curve of ANXA2 was 0.865; the cut-off value was established to be 18 ng/mL with a diagnostic sensitivity of 74% and a specificity of 88%, while the sensitivity and specificity of AFP at the cut-off value of 200 ng/dL were 20% and 100%, respectively. CONCLUSION: Serum ANXA2 may serve as a biomarker for the early detection of HCC.
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spelling pubmed-53686242017-04-10 Annexin A2 as a biomarker for hepatocellular carcinoma in Egyptian patients Shaker, Mohamed K Abdel Fattah, Hanzada I Sabbour, Ghada S Montasser, Iman F Abdelhakam, Sara M El Hadidy, Eman Yousry, Rehab El Dorry, Ahmed K World J Hepatol Case Control Study AIM: To investigate the clinical utility of serum annexin A2 (ANXA2) as a diagnostic marker for early hepatocellular carcinoma (HCC). METHODS: This study was performed in HCC Clinic of Ain Shams University Hospitals, Cairo, Egypt and included: Group 1: Fifty patients with early stage HCC (Barcelona Clinic Liver Cancer stage A); Group 2: Twenty five patients with chronic liver disease; and Control Group: Fifteen healthy, age- and sex-matched subjects who were seronegative for viral hepatitis markers. The following laboratory investigations were done: Viral hepatitis markers [hepatitis B surface antigen and hepatitis C virus (HCV) antibodies], HCV RNA in HCV antibody-positive patients, serum alpha fetoprotein (AFP), and serum ANXA2 levels. RESULTS: In this study, 88% of HCC patients (n = 44) were HCV-positive, while HBV infection represented only 8% of all HCC patients (n = 4); and two patients were negative for both viral markers. A highly significant difference was found between patients with HCC and chronic liver disease as well as controls with regard to serum ANXA2 levels (130, IQR 15-240; 15, IQR 15-17; and 17, IQR 15-30 ng/mL, respectively). The area under the curve of ANXA2 was 0.865; the cut-off value was established to be 18 ng/mL with a diagnostic sensitivity of 74% and a specificity of 88%, while the sensitivity and specificity of AFP at the cut-off value of 200 ng/dL were 20% and 100%, respectively. CONCLUSION: Serum ANXA2 may serve as a biomarker for the early detection of HCC. Baishideng Publishing Group Inc 2017-03-28 2017-03-28 /pmc/articles/PMC5368624/ /pubmed/28396717 http://dx.doi.org/10.4254/wjh.v9.i9.469 Text en ©The Author(s) 2017. 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 Case Control Study
Shaker, Mohamed K
Abdel Fattah, Hanzada I
Sabbour, Ghada S
Montasser, Iman F
Abdelhakam, Sara M
El Hadidy, Eman
Yousry, Rehab
El Dorry, Ahmed K
Annexin A2 as a biomarker for hepatocellular carcinoma in Egyptian patients
title Annexin A2 as a biomarker for hepatocellular carcinoma in Egyptian patients
title_full Annexin A2 as a biomarker for hepatocellular carcinoma in Egyptian patients
title_fullStr Annexin A2 as a biomarker for hepatocellular carcinoma in Egyptian patients
title_full_unstemmed Annexin A2 as a biomarker for hepatocellular carcinoma in Egyptian patients
title_short Annexin A2 as a biomarker for hepatocellular carcinoma in Egyptian patients
title_sort annexin a2 as a biomarker for hepatocellular carcinoma in egyptian patients
topic Case Control Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368624/
https://www.ncbi.nlm.nih.gov/pubmed/28396717
http://dx.doi.org/10.4254/wjh.v9.i9.469
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