Dissertation > Excellent graduate degree dissertation topics show
Gene Polymorphism of Myeloperoxidase and Genetic Susceptibility to Essential Hypertension
Author: ZhangZhiMing
Tutor: MaLiYa
School: Lanzhou University
Course: Department of Cardiology
Keywords: Essential Hypertension Myeloperoxidase Gene polymorphism Genetic susceptibility
CLC: R544.1
Type: Master's thesis
Year: 2007
Downloads: 48
Quote: 0
Read: Download Dissertation
Abstract
|
BACKGROUND & OBJECTIVE: A-463 bp G/A polymorphism is located in the promoter region of myeloperoxidase(MPO)gene was found to be associated with bioavailability of NO. However, its association with Essential Hypertension remained unclear. The aim of this study was designed to explore this association in Chinese population.METHODS: MPO genotypes’ in 107 cases of essential hypertension and 97 persons of healthy control were detected using PCR-restriction fragment length polymorphism assay(PCR-RFLP) in a case-control molecular epidemiology study. The association between this gene polymorphism and the risk of Essential Hypertension in Chinese population was examined through comparing odds ratio (OR)and 95% confidence interval (CI) between two groups.RESULTS: In healthy control group, the frequencies of persons carrying G/G, G/A, and A/A genotypes were 56.7% , 40.2% , and 3.1%, respectively . In Essential Hypertension group , the frequencies of the persons carrying above three genotypes were 70.1% , 29.0% , and 0.9% , respectively. There was significant diference of the frequencies of G/A genotype between two groups (P <0. 05), the risk of Essential Hypertension for person carrying G/G genotype was 1.79 fold of the persons carrying at least one A allele (95% Cl 1.005~3.186).CONCLUSION : MPO gene polymorphism was associated with susceptibility of Essential Hypertension in Chinese population. The risk of Essential Hypertension was decreased in the persons carrying allele A.
|
Related Dissertations
- CYP2C19 Gene Polymorphism in Patients with Ischemic Cerebrovascular,R743
- The Relationship of Polymorphisms of Methionine Synthase Reductase(MTRR) Gene and Plasma Homocysteine Levels with Myocardial Infarction,R542.22
- Clinical Study on Relationship Among Syndrome Differentiation Clssified in Tcm,ambulatory Blood Pressure Monitoring and Transcranial Doppler in Essential Hypertension,R259
- Preliminary Study of Molecular Epidemiology on Hepatitis B among Certain Regions in Anhui Province,R512.62
- Heterogeneity and Meta Analysis of the Essential Hypertension Risk Assessments,R544.1
- Association of Interleukin-6 Gene Polymorphisms with Susceptibility to Coronary Heart Disease in Asian Populations: a Meta-analysis,R541.4
- Effects of Telmisartan on hs-CRP and HMW-adiponectinin Patients with Essential Hypertension,R544.1
- Study of the Expression of Toll-like Receptor 2, 4mRNA and Polymorphisms of Patients with Leprosy,R755
- MDR1 and CYP3A gene polymorphisms on digoxin plasma concentrations of,R96
- MPO, IL-18 and INF-γ expression in human coronary arteries with plaque stability and preliminary study,R541.4
- Preliminary Study of Left Atrial Volume and Left Ventricular Volume Changes in Essential Hypertensive Elderly Patients,R544.1
- SLC2A9 gene eighth exon 137A / G polymorphism and diabetic patients with hyperuricemia relationship,R587.1
- The Expression of DNA Adducts dA in Chronic Atrophis Gastritis, Precancerous Lesions and Gastric Cancer and the Relationship with the CYP2E1 Gene Polymorphism,R735.2
- The Influence of Innate Immune Molecules and Cells in the Pathogenesis of Autoimmune Disease in Central Nervous System,R392
- Application of SYBR Green I Real-time PCR in ABO Genotyping,R440
- Effects of Lidocaine on Liver Injury Induced by Intestinal Ischemia-Reperfusion in Young Rats,R965
- The Correlation Research between the Gene Polymorphisms of Five CYP450 Isoforms of Enzymes and the Differences of Metabolic Ratio of Cocktail Probes,R969.1
- The Polymorphism of Sites 373 and 1688 of PECAM-1 Gene in Mucocutaneous Lymph Node Syndrome in Children,R758.6
- Relationship between Polymorphism of NAT1、NAT2 and ACE Gene and Hair Dye Dermatitis,R758.2
- Association between Genetic Polymorphisms of the FP Receptor (Prostaglandin F2α Receptor) Gene and Response to Latanoprost,R775
- CHD patients with depression nitric oxide synthase gene G894T polymorphism,R749.4
CLC: > Medicine, health > Internal Medicine > Heart, blood vessels ( circulatory ) disease > Abnormal blood pressure > Hypertension
© 2012 www.DissertationTopic.Net Mobile
|