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العنوان
Osteocalcin Level
In Patients With chronic Hepatitis
‛C’ /
المؤلف
kamel, Rasha Mohammed.
هيئة الاعداد
باحث / رشا محمد كامل
مشرف / أسامه سعد الشاعر
مشرف / إبراهيم محمد السعيد راجح
مناقش / خالد مصطفى بلال
مناقش / أيمن محمد البدوي
الموضوع
Hepatitis, chronic. Chronic active hepatitis. Osteocalcin.
تاريخ النشر
2015.
عدد الصفحات
195 p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الكيمياء الحيوية (الطبية)
تاريخ الإجازة
1/1/2015
مكان الإجازة
جامعة بنها - كلية طب بشري - Clinical And Chemical Pathology
الفهرس
Only 14 pages are availabe for public view

from 16

from 16

Abstract

Egypt has the largest burden of HCV infection in the world, with a 10
% prevalence of chronic HCV infection among persons aged 15-59 years
(El-Zanaty and way., 2008).
Metabolic bone disease is a significant disorder which appears in patients with chronic hepatopathy (also known as HO), especially in those affected by chronic cholestasis. Its etiology is complex and multifactorial and manifest as osteopenia and osteoprosis. This bone disorder must be evaluated and detected early in all patients with chronic liver disease in order to minimize the risk of fractures and improve their clinical progression and quality of life (Sanchez etal., 2006).
All currently available therapies for treatment of chronic HCV are based on the activity of group of biological agents called alpha interferon (Keam and Cvetikovic., 2008).
The estimated cost of care and treatment program for the Egyptian government is $80 million annually, which covers 40% of total costs of the program; the remaining 60% is paid by insurance companies and patients (Ford etal., 2012).
INF has been shown to be effective in inducing inhibition of viral replication, normalization of liver tests and even improvement of liver histology in HCV-related liver diseases and it is known that INF-α may affect bone turnover. There is limited information about the long term effect of INF-α therapy on bone metabolism (Lee and Karsety., 2009).
Osteocalcin is the most abundant non collagenous protein of bone
matrix (Razzaque., 2011). It is a product of differentiated osteoblast.