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Serum and Ascitic Fluid Hepcidin in HCV Positive Liver Cirrhosis with and without HCC

Received: 11 December 2013     Published: 10 January 2014
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Abstract

Background & Aim: Chronic HCV infection suppresses hepatic hepcidin expression which may enhance iron toxicity and lead to disease progression and HCC development. The aim of the study is to investigate the role of hepcidin in HCV+ve liver cirrhosis patients in relation to disease progression and HCC development. Patients and methods: The study population consists of: 20 HCV+ve patients without HCC (HCV patients), 20 HCV+ve patients with HCC (HCV-HCC patients) and 10 controls. In addition to comprehensive clinical examination, they were subjected to laboratory check-up for albumin, bilirubin, PT %, ferritin, AFP and hepcidin. Ascitic fluid hepcidin was done for all patients. Results: There was a significant difference among HCV and HCV-HCC patients and controls with regard serum ferritin and hepcidin (P = 0.001 & 0.0001 respectively). Serum hepcidin of HCV and HCV-HCC patients were significantly lower than controls (P = 0.0001). Serum and ascitic fluid hepcidin of HCV-HCC patients was significantly lower than HCV patients (P = 0.01 & 0.02 respectively). Serum ferritin was significantly higher in HCV and HCV-HCC patients than controls (P = 0.001). Serum ferritin of HCV-HCC patients was significantly higher than HCV patients (P = 0.02). Ascitic fluid hepcidin was negatively correlated with Child-Pugh score in HCV (r=-0.55 & P=0.01) and HCV-HCC patients (r = -0.53 & P = 0.02). Ascitic fluid hepcidin was negatively correlated with bilirubin in HCV (r = -0.43 & P=0.04) and HCV-HCC patients (r = -0.47 & P=0.04). Ascitic fluid hepcidin was positively correlated with serum albumin in HCV (r = +0.44 & P=0.04) but there was no correlation in HCV-HCC patients (r =-0.1 & P=0.7). Conclusion: Low levels of hepcidin may be involved in the pathophysiologic mechanism of iron overload in patients with chronic HCV with and without HCC. Moreover, there is a positive relationship between hepcidin levels and synthetic liver function suggesting that uniform suppression of hepcidin may be linked to disease progression and HCC development. Further analysis is still required to evaluate its usefulness as a marker for early detection of HCC by serial measurement of hepcidin in blood and ascitic fluid.

Published in European Journal of Preventive Medicine (Volume 1, Issue 3)
DOI 10.11648/j.ejpm.20130103.13
Page(s) 63-69
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2014. Published by Science Publishing Group

Keywords

Hepcidin, HCC, HCV, Ferritin

References
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Cite This Article
  • APA Style

    Ehab Abd El Atti, Alaa Dawood, Abdallah Said Essa, Bassam Mohamed Masoud, Enas Said Essa, et al. (2014). Serum and Ascitic Fluid Hepcidin in HCV Positive Liver Cirrhosis with and without HCC. European Journal of Preventive Medicine, 1(3), 63-69. https://doi.org/10.11648/j.ejpm.20130103.13

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    Ehab Abd El Atti; Alaa Dawood; Abdallah Said Essa; Bassam Mohamed Masoud; Enas Said Essa, et al. Serum and Ascitic Fluid Hepcidin in HCV Positive Liver Cirrhosis with and without HCC. Eur. J. Prev. Med. 2014, 1(3), 63-69. doi: 10.11648/j.ejpm.20130103.13

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    AMA Style

    Ehab Abd El Atti, Alaa Dawood, Abdallah Said Essa, Bassam Mohamed Masoud, Enas Said Essa, et al. Serum and Ascitic Fluid Hepcidin in HCV Positive Liver Cirrhosis with and without HCC. Eur J Prev Med. 2014;1(3):63-69. doi: 10.11648/j.ejpm.20130103.13

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  • @article{10.11648/j.ejpm.20130103.13,
      author = {Ehab Abd El Atti and Alaa Dawood and Abdallah Said Essa and Bassam Mohamed Masoud and Enas Said Essa and Yasser El-Ghobashy and Ashraf Anas Zytoon},
      title = {Serum and Ascitic Fluid Hepcidin in HCV Positive Liver Cirrhosis with and without HCC},
      journal = {European Journal of Preventive Medicine},
      volume = {1},
      number = {3},
      pages = {63-69},
      doi = {10.11648/j.ejpm.20130103.13},
      url = {https://doi.org/10.11648/j.ejpm.20130103.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ejpm.20130103.13},
      abstract = {Background & Aim: Chronic HCV infection suppresses hepatic hepcidin expression which may enhance iron toxicity and lead to disease progression and HCC development. The aim of the study is to investigate the role of hepcidin in HCV+ve liver cirrhosis patients in relation to disease progression and HCC development. Patients and methods: The study population consists of: 20 HCV+ve patients without HCC (HCV patients), 20 HCV+ve patients with HCC (HCV-HCC patients) and 10 controls. In addition to comprehensive clinical examination, they were subjected to laboratory check-up for albumin, bilirubin, PT %, ferritin, AFP and hepcidin. Ascitic fluid hepcidin was done for all patients. Results: There was a significant difference among HCV and HCV-HCC patients and controls with regard serum ferritin and hepcidin (P = 0.001 & 0.0001 respectively). Serum hepcidin of HCV and HCV-HCC patients were significantly lower than controls (P = 0.0001). Serum and ascitic fluid hepcidin of HCV-HCC patients was significantly lower than HCV patients (P = 0.01 & 0.02 respectively). Serum ferritin was significantly higher in HCV and HCV-HCC patients than controls (P = 0.001). Serum ferritin of HCV-HCC patients was significantly higher than HCV patients (P = 0.02). Ascitic fluid hepcidin was negatively correlated with Child-Pugh score in HCV (r=-0.55 & P=0.01) and HCV-HCC patients (r = -0.53 & P = 0.02). Ascitic fluid hepcidin was negatively correlated with bilirubin in HCV (r = -0.43 & P=0.04) and HCV-HCC patients (r = -0.47 & P=0.04). Ascitic fluid hepcidin was positively correlated with serum albumin in HCV (r = +0.44 & P=0.04) but there was no correlation in HCV-HCC patients (r =-0.1 & P=0.7). Conclusion: Low levels of hepcidin may be involved in the pathophysiologic mechanism of iron overload in patients with chronic HCV with and without HCC. Moreover, there is a positive relationship between hepcidin levels and synthetic liver function suggesting that uniform suppression of hepcidin may be linked to disease progression and HCC development. Further analysis is still required to evaluate its usefulness as a marker for early detection of HCC by serial measurement of hepcidin in blood and ascitic fluid.},
     year = {2014}
    }
    

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  • TY  - JOUR
    T1  - Serum and Ascitic Fluid Hepcidin in HCV Positive Liver Cirrhosis with and without HCC
    AU  - Ehab Abd El Atti
    AU  - Alaa Dawood
    AU  - Abdallah Said Essa
    AU  - Bassam Mohamed Masoud
    AU  - Enas Said Essa
    AU  - Yasser El-Ghobashy
    AU  - Ashraf Anas Zytoon
    Y1  - 2014/01/10
    PY  - 2014
    N1  - https://doi.org/10.11648/j.ejpm.20130103.13
    DO  - 10.11648/j.ejpm.20130103.13
    T2  - European Journal of Preventive Medicine
    JF  - European Journal of Preventive Medicine
    JO  - European Journal of Preventive Medicine
    SP  - 63
    EP  - 69
    PB  - Science Publishing Group
    SN  - 2330-8230
    UR  - https://doi.org/10.11648/j.ejpm.20130103.13
    AB  - Background & Aim: Chronic HCV infection suppresses hepatic hepcidin expression which may enhance iron toxicity and lead to disease progression and HCC development. The aim of the study is to investigate the role of hepcidin in HCV+ve liver cirrhosis patients in relation to disease progression and HCC development. Patients and methods: The study population consists of: 20 HCV+ve patients without HCC (HCV patients), 20 HCV+ve patients with HCC (HCV-HCC patients) and 10 controls. In addition to comprehensive clinical examination, they were subjected to laboratory check-up for albumin, bilirubin, PT %, ferritin, AFP and hepcidin. Ascitic fluid hepcidin was done for all patients. Results: There was a significant difference among HCV and HCV-HCC patients and controls with regard serum ferritin and hepcidin (P = 0.001 & 0.0001 respectively). Serum hepcidin of HCV and HCV-HCC patients were significantly lower than controls (P = 0.0001). Serum and ascitic fluid hepcidin of HCV-HCC patients was significantly lower than HCV patients (P = 0.01 & 0.02 respectively). Serum ferritin was significantly higher in HCV and HCV-HCC patients than controls (P = 0.001). Serum ferritin of HCV-HCC patients was significantly higher than HCV patients (P = 0.02). Ascitic fluid hepcidin was negatively correlated with Child-Pugh score in HCV (r=-0.55 & P=0.01) and HCV-HCC patients (r = -0.53 & P = 0.02). Ascitic fluid hepcidin was negatively correlated with bilirubin in HCV (r = -0.43 & P=0.04) and HCV-HCC patients (r = -0.47 & P=0.04). Ascitic fluid hepcidin was positively correlated with serum albumin in HCV (r = +0.44 & P=0.04) but there was no correlation in HCV-HCC patients (r =-0.1 & P=0.7). Conclusion: Low levels of hepcidin may be involved in the pathophysiologic mechanism of iron overload in patients with chronic HCV with and without HCC. Moreover, there is a positive relationship between hepcidin levels and synthetic liver function suggesting that uniform suppression of hepcidin may be linked to disease progression and HCC development. Further analysis is still required to evaluate its usefulness as a marker for early detection of HCC by serial measurement of hepcidin in blood and ascitic fluid.
    VL  - 1
    IS  - 3
    ER  - 

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Author Information
  • Internal Medicine Department, Faculty of Medicine, Menoufiya University, Egypt

  • Internal Medicine Department, Faculty of Medicine, Menoufiya University, Egypt

  • Tropical Medicine Department, Faculty of Medicine, Menoufiya University, Egypt

  • Tropical Medicine Department, Faculty of Medicine, Menoufiya University, Egypt

  • Clinical Pathology Department, Faculty of Medicine, Menoufiya University, Egypt

  • Biochemistry Department, Faculty of Medicine, Menoufiya University, Egypt

  • Radiology Department, Faculty of Medicine, Menoufiya University, Egypt

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