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Urinary podocyte-associated mRNA profile in Egyptian type 2 diabetic patients with diabetic nephropathy / Iman Abdulrahman Tohamy Zanoon; Supervised Mohamed Gamal Eldin Saadi , Hala Essam Eldin Kahla , Mervat Saad Elansary

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Iman Abdulrahman Tohamy Zanoon , 2016Description: 171 P. : facsimiles ; 25cmOther title:
  • الحمض النووى الريبوزومى الرسول المصاحب لخلايا رجلاء "البودوسايت" فى بول مرضى السكرى "من النوع الثانى" المصريين و المصابين بمرض اعتلال الكلى السكرى [Added title page title]
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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Internal Medicine Summary: Background: Microalbuminuria is still regarded as the gold standard for diagnosing of DN, however its predictive powers are very limited. Also microalbuminuria is a nonspecific indicator of many forms of kidney injury. Thus, there is a substantial need for a biomarker that may enable detection of diabetic nephropathy at an earlier stage with higher accuracy. A biomarker derived from the urine is particularly useful, as it has the advantages of being a simple, noninvasive test and is a direct conduit to the site of injury. Podocyte injury and subsequent excretion in urine play a crucial role in the pathogenesis and progression of diabetic nephropathy (DN). Quantification of messenger RNA expression in urinary sediment by real-time PCR is emerging as a noninvasive method of screening DN-associated biomarkers. Objectives: the aim of our work is to study the expression of podocyte-associated genes in urinary sediment and their relation to disease severity in type 2 diabetic Egyptian patients with diabetic nephropathy. Subjects and methods: Diabetic patients (n=60) and healthy controls (n=20) were enrolled in this study. Diabetic patients were divided- according to their urinary albumin excretion (UAE)-into a normoalbuminuria group (UAE less than 30 mg/g, n=20), a microalbuminuria group (UAE between 30 and 300 mg/g, n=20), and a macroalbuminuria group (UAE more than 300 mg/g, n=20). Relative mRNA abundance of nephrin, podocalyxin, and podocin were quantified, and correlations between target mRNAs and clinical parameters were examined
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.18.Ph.D.2016.Im.U (Browse shelf(Opens below)) Not for loan 01010110073125000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.18.Ph.D.2016.Im.U (Browse shelf(Opens below)) 73125.CD Not for loan 01020110073125000

Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Internal Medicine

Background: Microalbuminuria is still regarded as the gold standard for diagnosing of DN, however its predictive powers are very limited. Also microalbuminuria is a nonspecific indicator of many forms of kidney injury. Thus, there is a substantial need for a biomarker that may enable detection of diabetic nephropathy at an earlier stage with higher accuracy. A biomarker derived from the urine is particularly useful, as it has the advantages of being a simple, noninvasive test and is a direct conduit to the site of injury. Podocyte injury and subsequent excretion in urine play a crucial role in the pathogenesis and progression of diabetic nephropathy (DN). Quantification of messenger RNA expression in urinary sediment by real-time PCR is emerging as a noninvasive method of screening DN-associated biomarkers. Objectives: the aim of our work is to study the expression of podocyte-associated genes in urinary sediment and their relation to disease severity in type 2 diabetic Egyptian patients with diabetic nephropathy. Subjects and methods: Diabetic patients (n=60) and healthy controls (n=20) were enrolled in this study. Diabetic patients were divided- according to their urinary albumin excretion (UAE)-into a normoalbuminuria group (UAE less than 30 mg/g, n=20), a microalbuminuria group (UAE between 30 and 300 mg/g, n=20), and a macroalbuminuria group (UAE more than 300 mg/g, n=20). Relative mRNA abundance of nephrin, podocalyxin, and podocin were quantified, and correlations between target mRNAs and clinical parameters were examined

Issued also as CD

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