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Investigation of the correlation between norepinephrine transporter gene polymorphisms and essential hypertension

机译:去甲肾上腺素转运蛋白基因多态性与原发性高血压的相关性研究

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Essential hypertension (EH) is an etiological risk factor that poses a serious threat to human health. The aim of this study therefore was to investigate the correlation between the two SNPs (rs1805067 and rs2397771) of the norepinephrine (NE) transporter gene in the sympathetic nervous system and essential hypertension (EH). A total of 96 hypertensive patients (EH group) and 96 normal subjects (control group) were selected by epidemiological investigation and the sequences at rs1805067 and rs2397771 in the two groups were investigated using polymerase chain reaction (PCR) and Sanger sequencing. In the EH group, systolic and diastolic blood pressure, body mass index (BMI), levels of creatinine, low-density lipoprotein cholesterol (LDL-C), triglycerides (TG), and the percentage of drinkers were found to be higher compared with those of the control group (P<0.05). The results of the analysis of the allele frequencies of rs1805067 (A/G) revealed that there was no difference between the two groups (P>0.05). The analysis results of the allele frequencies of rs2397771 (C/G) in the EH group revealed that G accounted for 48.96% and C for 51.04% of the patients, while in the control group, these values were 64.58 and 35.42%, respectively. These results indicated a significant difference between the two groups (P<0.05). In the population studied, the onset of EH may be correlated with BMI. TG, LDL-C and high-density lipoprotein cholesterol (HDL-C). EH may be related to the rs2397771 (C/G) C allele polymorphism of the NE transporter gene but not to rs1805067 (A/G).
机译:原发性高血压(EH)是一种病因危险因素,对人类健康构成严重威胁。因此,本研究的目的是研究交感神经系统中去甲肾上腺素(NE)转运蛋白基因的两个SNP(rs1805067和rs2397771)之间的相关性。通过流行病学调查,共选择了96例高血压患者(EH组)和96例正常受试者(对照组),并使用聚合酶链反应(PCR)和Sanger测序研究了两组中rs1805067和rs2397771的序列。在EH组中,发现收缩压和舒张压,体重指数(BMI),肌酐水平,低密度脂蛋白胆固醇(LDL-C),甘油三酸酯(TG)和饮酒者的百分比高于对照组(P <0.05)。 rs1805067(A / G)等位基因频率的分析结果表明,两组之间没有差异(P> 0.05)。 EH组rs2397771(C / G)等位基因频率的分析结果显示,G占患者的48.96%,C占51.04%,而对照组的这些值分别为64.58和35.42%。这些结果表明两组之间有显着差异(P <0.05)。在所研究的人群中,EH的发作可能与BMI相关。 TG,LDL-C和高密度脂蛋白胆固醇(HDL-C)。 EH可能与NE转运蛋白基因的rs2397771(C / G)C等位基因多态性相关,但与rs1805067(A / G)不相关。

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