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Zaher, Ebtsam, Ghazal, Abeer, Ellabban, Wael, El-Deeb, Mona, Al-Ghaleed, Lamyaa. (1397). Predictive Markers for Hepatocellular Carcinoma Development in Patients with Chronic Hepatitis C Virus Genotype4a. سامانه مدیریت نشریات علمی, 9(4), 261-273. doi: 10.30476/mejc.2018.42132
Ebtsam Zaher; Abeer A. Ghazal; Wael A. Ellabban; Mona El-Deeb; Lamyaa Al-Ghaleed. "Predictive Markers for Hepatocellular Carcinoma Development in Patients with Chronic Hepatitis C Virus Genotype4a". سامانه مدیریت نشریات علمی, 9, 4, 1397, 261-273. doi: 10.30476/mejc.2018.42132
Zaher, Ebtsam, Ghazal, Abeer, Ellabban, Wael, El-Deeb, Mona, Al-Ghaleed, Lamyaa. (1397). 'Predictive Markers for Hepatocellular Carcinoma Development in Patients with Chronic Hepatitis C Virus Genotype4a', سامانه مدیریت نشریات علمی, 9(4), pp. 261-273. doi: 10.30476/mejc.2018.42132
Zaher, Ebtsam, Ghazal, Abeer, Ellabban, Wael, El-Deeb, Mona, Al-Ghaleed, Lamyaa. Predictive Markers for Hepatocellular Carcinoma Development in Patients with Chronic Hepatitis C Virus Genotype4a. سامانه مدیریت نشریات علمی, 1397; 9(4): 261-273. doi: 10.30476/mejc.2018.42132

Predictive Markers for Hepatocellular Carcinoma Development in Patients with Chronic Hepatitis C Virus Genotype4a

Middle East Journal of Cancer
مقاله 1، دوره 9، شماره 4، دی 2018، صفحه 261-273    اصل مقاله (208.05 K)
نوع مقاله: Original Article(s)
شناسه دیجیتال (DOI): 10.30476/mejc.2018.42132
نویسندگان
Ebtsam Zaher* 1؛ Abeer A. Ghazal2؛ Wael A. Ellabban3؛ Mona El-Deeb4؛ Lamyaa Al-Ghaleed5
1Radiation Sciences Department, Medical Research Institute, Alexandria University, Alexandria, Egypt
2Microbiology Department, Medical Research Institute, Alexandria University, Alexandria, Egypt
3Queen’s Medical Center, Durham, UK
4Clinical Pathology Department, Medical Research Institute, Alexandria University, Alexandria, Egypt
5Internal Medicine Department, Medical Research Institute, Alexandria University, Alexandria, Egypt
چکیده
Background: Egypt has the highest prevalence of hepatitis C virus worldwide. Monitoring hepatitis C-infected patients for hepatocellular carcinoma development is an important clinical issue to diagnose these patients during the potentially curable early-stage of disease. This study aims to evaluate the role of N-terminal procollagen III, matrix metalloproteinase- 2, tissue inhibitor of matrix metalloproteinase-1, alpha-fetoprotein, and conventional liver function tests as predictors of hepatocellular carcinoma development upon long-term followup of non-responding hepatitis C virus patients.Methods: The study included 850 treatment-naïve hepatitis C virus genotype 4a adult patients; after treatment, 360 achieved sustained viral response while 490 did not. Nonresponding patients had a 5-year rate for hepatocarcinogenesis of 8.4% and a 10-year rate of 27.5%. N-terminal procollagen III, matrix metalloproteinase-2, tissue inhibitor of matrix metalloproteinase-1, alpha-fetoprotein, and conventional liver function tests were evaluated in all patients before and after treatment, and after hepatocellular carcinoma development. The study also included a group of 50 hepatocellular carcinoma patients who were negative for hepatitis C and hepatitis B viruses, and a group of 50 healthy subjects as controls.Results: The non-responders had significantly higher age, stage, grade, viral load, alanine aminotransferase, and aspartate aminotransferase than responders. Also N-terminal procollagen III, matrix metalloproteinase-2, tissue inhibitor of matrix metalloproteinase-1, and alphafetoprotein were significantly higher in non-responders; after treatment they decreased in responders. In non-responders they remained higher than the control. The most significant risk factors for hepatocellular carcinoma development in non-responding hepatitis C virus patients were male gender and increased age, stage, grade, aspartate aminotransferase, Nterminal procollagen III, and tissue inhibitor of matrix metalloproteinase-1. Patients with viral-hepatocellular carcinoma were of significantly lower age, higher grade, stage, γ-glutamyltransferase, N-terminal procollagen III, and matrix metalloproteinase-2 than non-viral hepatocellular carcinoma patients. Percent positive N-terminal procollagen III, tissue inhibitor of matrix metalloproteinase-1, and alpha-fetoprotein were significantly higher in viral hepatocellular carcinoma patients.Conclusion: Data suggest that high N-terminal procollagen III and tissue inhibitor of matrix metalloproteinase-1levels after treatment might be particularly important as markers of hepatitis C virus-non-responding patients who are at higher risk of developing hepatocellular carcinoma, especially in older males with high stage and grade liver disease. However, studies of larger scale are needed to verify this suggestion.
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