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Serum alpha-fetoprotein level is higher in hepatitis C than hepatitis B infected chronic liver disease patients
BACKGROUND: The frequency of raised serum alpha-fetoprotein may vary in relation to hepatitis B or C infection in chronic liver disease (CLD). The study evaluated the frequency of hepatitis B and C in patients with chronic liver disease and correlated the levels of serum alpha-fetoprotein with hepat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948968/ https://www.ncbi.nlm.nih.gov/pubmed/24665160 http://dx.doi.org/10.4103/0300-1652.126302 |
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author | Emokpae, Mathias Abiodun Adejumol, Babatunde Gabriel Abdu, Aliyu Sadiq, Nasiru Magaji |
author_facet | Emokpae, Mathias Abiodun Adejumol, Babatunde Gabriel Abdu, Aliyu Sadiq, Nasiru Magaji |
author_sort | Emokpae, Mathias Abiodun |
collection | PubMed |
description | BACKGROUND: The frequency of raised serum alpha-fetoprotein may vary in relation to hepatitis B or C infection in chronic liver disease (CLD). The study evaluated the frequency of hepatitis B and C in patients with chronic liver disease and correlated the levels of serum alpha-fetoprotein with hepatitis B and C infection in the patients. MATERIALS AND METHODS: Eighty-six patients with CLD were recruited for the study. Fifty subjects, with no CLD were used as control. Hepatitis B surface Antigen (HBsAg) and hepatitis C antibody were determined using enzyme-linked immunosorbent assay (ELISA) technique (Human diagnostics, Germany and HCV Murex 40 Anhet laboratories, USA) while liver function tests were evaluated using express plus chemistry auto analyzer. Alpha-fetoprotein was assayed using ELECSYS 1010 auto analyser. RESULTS: There were 60 males and 26 females, with a mean age of 46 + 6.5 years, while the controls were 25 males and 25 females with a mean age of 41 ± 2.5 years. Thirty-six subjects (41.7%) were seropositive for HBsAg while 24 (27.9%) were seropositive for Hepatitis C Virus (HCV) antibody. The mean alpha fetoprotein level was 359 ± 9.9 ng/mL while mean control value was 1.93 ± 0.24 ng/mL. Liver function test parameters were elevated compared with control subjects (P < 0.001). The increase in serum alpha-fetoprotein was higher (P < 0.001) in HCV than HBsAg positive patients. CONCLUSION: Serum alpha-fetoprotein level was highest in HCV compared to HBsAg positive and hepatitis negative patients with CLD. |
format | Online Article Text |
id | pubmed-3948968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-39489682014-03-24 Serum alpha-fetoprotein level is higher in hepatitis C than hepatitis B infected chronic liver disease patients Emokpae, Mathias Abiodun Adejumol, Babatunde Gabriel Abdu, Aliyu Sadiq, Nasiru Magaji Niger Med J Original Article BACKGROUND: The frequency of raised serum alpha-fetoprotein may vary in relation to hepatitis B or C infection in chronic liver disease (CLD). The study evaluated the frequency of hepatitis B and C in patients with chronic liver disease and correlated the levels of serum alpha-fetoprotein with hepatitis B and C infection in the patients. MATERIALS AND METHODS: Eighty-six patients with CLD were recruited for the study. Fifty subjects, with no CLD were used as control. Hepatitis B surface Antigen (HBsAg) and hepatitis C antibody were determined using enzyme-linked immunosorbent assay (ELISA) technique (Human diagnostics, Germany and HCV Murex 40 Anhet laboratories, USA) while liver function tests were evaluated using express plus chemistry auto analyzer. Alpha-fetoprotein was assayed using ELECSYS 1010 auto analyser. RESULTS: There were 60 males and 26 females, with a mean age of 46 + 6.5 years, while the controls were 25 males and 25 females with a mean age of 41 ± 2.5 years. Thirty-six subjects (41.7%) were seropositive for HBsAg while 24 (27.9%) were seropositive for Hepatitis C Virus (HCV) antibody. The mean alpha fetoprotein level was 359 ± 9.9 ng/mL while mean control value was 1.93 ± 0.24 ng/mL. Liver function test parameters were elevated compared with control subjects (P < 0.001). The increase in serum alpha-fetoprotein was higher (P < 0.001) in HCV than HBsAg positive patients. CONCLUSION: Serum alpha-fetoprotein level was highest in HCV compared to HBsAg positive and hepatitis negative patients with CLD. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3948968/ /pubmed/24665160 http://dx.doi.org/10.4103/0300-1652.126302 Text en Copyright: © Nigerian Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Emokpae, Mathias Abiodun Adejumol, Babatunde Gabriel Abdu, Aliyu Sadiq, Nasiru Magaji Serum alpha-fetoprotein level is higher in hepatitis C than hepatitis B infected chronic liver disease patients |
title | Serum alpha-fetoprotein level is higher in hepatitis C than hepatitis B infected chronic liver disease patients |
title_full | Serum alpha-fetoprotein level is higher in hepatitis C than hepatitis B infected chronic liver disease patients |
title_fullStr | Serum alpha-fetoprotein level is higher in hepatitis C than hepatitis B infected chronic liver disease patients |
title_full_unstemmed | Serum alpha-fetoprotein level is higher in hepatitis C than hepatitis B infected chronic liver disease patients |
title_short | Serum alpha-fetoprotein level is higher in hepatitis C than hepatitis B infected chronic liver disease patients |
title_sort | serum alpha-fetoprotein level is higher in hepatitis c than hepatitis b infected chronic liver disease patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948968/ https://www.ncbi.nlm.nih.gov/pubmed/24665160 http://dx.doi.org/10.4103/0300-1652.126302 |
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