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العنوان
Detection of TNF-α as a Cofactor
in the Pathogenesis of Nasal Polypi
/
الناشر
Ain Shams University .
المؤلف
Ali,Zeinab Rezk Abd_elnazer .
هيئة الاعداد
باحث / زينب رزق عبد النظير على
مشرف / محمد عبد الروؤف
مشرف / طارق مصطفى كمال
مشرف / أحمد محمود معروف
تاريخ النشر
2020
عدد الصفحات
77.p;
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الحنجرة
تاريخ الإجازة
1/4/2020
مكان الإجازة
جامعة عين شمس - كلية الطب - Otorhinolaryngeology
الفهرس
Only 14 pages are availabe for public view

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from 77

Abstract

Background: Nasal Polyposis (NP) is a complex multi-factorial disease; associated with several environmental, genetic and inflammatory factors. TNF-alpha is one of the major pro-inflammatory cytokines involved in NP pathogenesis. Some of the polymorphisms of this gene affect its expression.
Aim of the Work: To evaluate the polymorphism of TNF-alpha G/A308 gene and its association with nasal polyposis in Egypt.
Patients and Methods: In this case-control study, 25 patients with NP and 25 healthy individuals referred to Ain Shams University hospital were evaluated. After DNA extraction, RFLP-PCR was used to determine polymorphism. Chi-square test was used to compare the frequency distribution of genotype and alleles of TNFalpha gene with NP. The frequency of genotype G/G, A/A and G/A in the NP group was 8, 40 and 52%, and in the control group was 76, 1 and 5 %, respectively.
Results: There was a statistically significant difference between genotype G/G in two groups (P = 0.0001). In addition, the frequency of allele A in patients and controls was 10 and 1%, respectively; and this difference was statistically significant (p = 0.0001). The findings of this study demonstrated that polymorphism in TNF-alpha gene might be a risk factor for NP in Egypt and the minor frequency of TNF-alpha G308A allele in the current study is slightly more than other major populations. However, more investigations with high number of population are necessary in future.
Conclusion: According to scientific evidence on TNF-α gene promoter G/A 308 polymorphism in Egypt, it seems that the pattern of genotypic distribution in all areas is the same. However, we found the greater amount of allele A in this study compared with the control group, and the occurrence of G/A genotype related to NP but for more valid results, a larger sample size is necessary. However on our results this polymorphism might be considered as a risk factor of susceptibility of NP in Egyptian people.