Asmaa Ahmed Ibrahim Elmonier

Genetic analysis of endoglin pathway components and their possible association with risk of preeclampsia in Egyptian women / التحليل الجينى لمكونات مسار الإندوجلين وإمكانية إرتباطهم بخطرالإصابة بتسمم الحمل فى السيدات المصريات Asmaa Ahmed Ibrahim Elmoniern ; Supervised Amira Abdelmonem Shaheen , Noha Ahmed Elboghdady - Cairo : Asmaa Ahmed Ibrahim Elmonier , 2019 - 82 P. : charts , facsimiles ; 25cm

Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Biochemistry

Introduction:Preeclampsia(PE)isapregnancy-specifichypertensivediseasewhose etiopathogenesis remains unclear. Objectives: This study was designed to assess association between PE and 3 single nucleotide polymorphisms (SNPs): ENG (G/A) rs11792480, TGFÝR1 (A/C) rs10739778 and TGFÝR2 (G/A) rs6550005, beside the circulating level of soluble endoglin (sENG), oxidative stress biomarkers and nitric oxide (NO) in Egyptian women. Methods: The study included 75 preeclamptic women stratified into 4 clinical subgroups and 50 normotensive pregnant women. Genotyping was performed by real time polymerase chain reaction-TaqMan allelic discrimination. Results: Preeclamptic women showed significantly increased sENG and malondialdehyde (MDA) levels, decreased total antioxidant capacity (TAC), endothelial nitric oxide synthase (eNOS) and NO levels, without change in transforming growth factor beta 1 (TGFÝ1) level versus controls. Moreover, sENG was significantly higher in severe than mild PE and in early- than late-onset PE. Higher MDA and lower TAC and NO levels were observed in severe than mild PE. ENG (G/A) and TGFÝR2 (G/A) showed no association with PE. However, CC genotype of TGFÝR1 (A/C) was more frequent in controls than either PE, early-onset or severe PE revealing a reduced PE risk in CC genotype versus AA or AA+AC. Importantly, patients carrying AA genotype had higher systolic blood pressure (SBP) and MDA with lower TAC level, gestational age (GA) at delivery and birth weight than those carrying CC genotype



Endoglin Polymorphism Preeclampsia