首页> 美国卫生研究院文献>Journal of Cardiovascular Development and Disease >Analysis of Angiotensin Converting Enzyme Endothelial Nitric Oxide Synthase Serotonin Gene Polymorphisms among Atrial Septal Defect Subjects with and without Pulmonary Arterial Hypertension
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Analysis of Angiotensin Converting Enzyme Endothelial Nitric Oxide Synthase Serotonin Gene Polymorphisms among Atrial Septal Defect Subjects with and without Pulmonary Arterial Hypertension

机译:患有和未患有肺动脉高压的房间隔缺损患者中血管紧张素转化酶内皮型一氧化氮合酶和血清素基因多态性的分析

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摘要

Genetic polymorphisms are variations in DNA sequences which can influence either disease susceptibility, severity, or prognosis. Pulmonary arterial hypertension (PAH) is one of the complications that occurs in certain patients who have atrial septal defect (ASD). This study seeks to determine the association of gene polymorphisms with the pathogenesis of PAH in ASD patients. This study was conducted on 30 ASD patients with PAH, and 50 ASD patients who were not diagnosed with PAH. All respondents were Malay. Patients were selected based on stringent inclusion and exclusion criteria. Molecular analyses were done to detect the genetic polymorphisms of angiotensin converting enzyme (ACE I/D), serotonin transporter (5-HTTLPR), endothelial nitric oxide synthase (eNOS) G894T, and eNOS 4b/4a. The genotypes of these genetic polymorphisms were determined using conventional PCR and PCR-RFLP methods. The PCR products were analysed using agarose gel electrophoresis. Statistical analysis was done using SPSS Version 22. Clinical characteristics, such as the diameter of ASD, mean arterial pressure (MAP), and mean pulmonary artery pressure (mPAP) differed significantly (p < 0.05). Based on the statistical analysis, ACE I/D, eNOS G894T, and eNOS 4b/4a do not contribute to the progression of PAH amongst ASD patients (p > 0.05). However, the L allele of the 5-HTTLPR gene polymorphism may have an affect on the development of PAH in ASD patients (p < 0.05).
机译:遗传多态性是DNA序列中的变异,可影响疾病的易感性,严重性或预后。肺动脉高压(PAH)是某些患有房间隔缺损(ASD)的患者所发生的并发症之一。这项研究旨在确定基因多态性与ASD患者PAH发病机制的关系。这项研究针对30名ASD PAH患者和50名未诊断为PAH的ASD患者进行。所有受访者均为马来人。根据严格的入选和排除标准选择患者。进行了分子分析,以检测血管紧张素转化酶(ACE I / D),血清素转运蛋白(5-HTTLPR),内皮型一氧化氮合酶(eNOS)G894T和eNOS 4b / 4a的遗传多态性。使用常规PCR和PCR-RFLP方法确定这些遗传多态性的基因型。使用琼脂糖凝胶电泳分析PCR产物。使用SPSS 22版进行统计分析。临床特征,例如ASD的直径,平均动脉压(MAP)和平均肺动脉压(mPAP)有显着差异(p <0.05)。根据统计分析,ACE I / D,eNOS G894T和eNOS 4b / 4a对ASD患者的PAH进程无贡献(p> 0.05)。但是,5-HTTLPR基因多态性的L等位基因可能会影响ASD患者PAH的发生(p <0.05)。

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