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العنوان
Assessing the relation between some genetic polymorphisms and autoimmune liver diseases in Egyptian patients /
الناشر
Salma Essam Mohammed Salah Eldin Said ,
المؤلف
Salma Essam Mohammed Salah Eldin Said
هيئة الاعداد
باحث / Salma Essam Mohammed Salaheldin Said
مشرف / Tarek M. Kamal Motawi
مشرف / Shohda A. El-Maraghy
مناقش / Sahar AbdElatty Sharaf
تاريخ النشر
2019
عدد الصفحات
86 P. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
Biochemistry
تاريخ الإجازة
13/6/2019
مكان الإجازة
جامعة القاهرة - كلية الصيدلة - Biochemistry
الفهرس
Only 14 pages are availabe for public view

from 126

from 126

Abstract

Background: Autoimmune liver diseases (AILDs) comprise three entities: autoimmune hepatitis (AIH), primary biliary cholangitis and primary sclerosing cholangitis. Although the pathogenesis of pediatric-onset autoimmune hepatitis (pAIH) remains incompletely understood, genetic variants and environmental factors are known to be involved. Caspase recruitment domain family member 10 (CARD10) is a scaffold protein that participates in a complex pathway activating nuclear factor kappa-B (NFmB) and tumor necrosis factor alpha (TNF-Ü). This study aimed to investigate the association of CARD10 rs6000782 (g.37928186A>C) and TNF gene promoter rs1799724 (c.-1037C>T) variants with pAIH susceptibility in a cohort of Egyptian children.The research was also extended to assess the relationship of these variants with levels of NFmB-p65 and TNF-Ü. Subjects and methods:Fifty-sixpAIH patients and 44 age- and sex-matched healthy controls were included. Variant genotyping was performed by polymerase chain reaction (PCR). Serum NFmB-p65 and TNF-Ü levels were measured using enzyme-linked immunosorbent assay (ELISA)