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The association of plasminogen activator inhibitor (PAI-1) Level and 4G/5G Gene polymorphism with diabetic nephropathy in type 2 diabetes mellitus / Nesma Mohamed Abdelraswool ; Supervised Manal Mohamed Kamal , Mai Mohsen Fawzi , Nahed Mohamed Ibrahim

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Nesma Mohamed Abdelraswool , 2015Description: 154 P. : facsimiles ; 25cmOther title:
  • علاقة مستوى مثبط محفز البلازمينوجين -1 فى الدم والتعدد الشكلى للجين 4ج/5ج فى مرضى البول السكرى المصابين بالقصور الكلوى [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology Summary: Background: Plasminogen activator inhibitor (PAI-1) is a regulatory enzyme of fibrinolytic system. Point mutation in PAI-1 is implicated in the pathogenesis of diabetic nephropathy (DN) in many ethinic groups. The aim of this study was to study the association of 4G/5G PAI-1 polymorphism as a risk factor of DN in type 2 diabetes mellitus (T2DM) patients. Subjects and Methods: The PAI-1 polymorphism was detected in 90 T2DM patients by SSP-PCR. They were divided into 2 groups: 45 patients without nephropathy, 45 patients with nephropathy. Plasma levels of PAI-1 were assayed by ELISA. Results: The genomic DNA analysis of (PAI-1) 4G/5G gene polymorphism (rs 1799889) revealed no statistically significant difference in distribution of different genotypes (P=1.0). The frequency of4G/4G genotype was (8.9 % & 11.1%), 4G/5G genotype was (48.9 % & 48.9 %) and 5G/5G genotype was (42.2% & 40%) in group I (diabetic patients without nephropathy) and group II (diabetic patients with nephropathy) respectively. Plasma levels of PAI-1 were not associated with PAI-1 mutation, also there was no significant association between PAI-1 level and DN (P=0.548). Conclusion: Plasminogen activator inhibitor-1 gene mutation was not associated with increased risk for diabetic nephropathy in type 2 diabetic patients and had no effect on plasma levels of PAI-1
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.M.Sc.2015.Ne.A (Browse shelf(Opens below)) Not for loan 01010110069075000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.M.Sc.2015.Ne.A (Browse shelf(Opens below)) 69075.CD Not for loan 01020110069075000

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology

Background: Plasminogen activator inhibitor (PAI-1) is a regulatory enzyme of fibrinolytic system. Point mutation in PAI-1 is implicated in the pathogenesis of diabetic nephropathy (DN) in many ethinic groups. The aim of this study was to study the association of 4G/5G PAI-1 polymorphism as a risk factor of DN in type 2 diabetes mellitus (T2DM) patients. Subjects and Methods: The PAI-1 polymorphism was detected in 90 T2DM patients by SSP-PCR. They were divided into 2 groups: 45 patients without nephropathy, 45 patients with nephropathy. Plasma levels of PAI-1 were assayed by ELISA. Results: The genomic DNA analysis of (PAI-1) 4G/5G gene polymorphism (rs 1799889) revealed no statistically significant difference in distribution of different genotypes (P=1.0). The frequency of4G/4G genotype was (8.9 % & 11.1%), 4G/5G genotype was (48.9 % & 48.9 %) and 5G/5G genotype was (42.2% & 40%) in group I (diabetic patients without nephropathy) and group II (diabetic patients with nephropathy) respectively. Plasma levels of PAI-1 were not associated with PAI-1 mutation, also there was no significant association between PAI-1 level and DN (P=0.548). Conclusion: Plasminogen activator inhibitor-1 gene mutation was not associated with increased risk for diabetic nephropathy in type 2 diabetic patients and had no effect on plasma levels of PAI-1

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