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探讨多巴胺 D1 受体基因多态性与土耳其人群原发性高血压的相关性。

Investigation of the association between dopamine D1 receptor gene polymorphisms and essential hypertension in a group of Turkish subjects.

机构信息

Marmara University School of Medicine, Department of Biophysics, Istanbul, Turkey.

出版信息

Clin Exp Hypertens. 2011;33(6):418-21. doi: 10.3109/10641963.2011.561898. Epub 2011 Jul 28.

DOI:10.3109/10641963.2011.561898
PMID:21797797
Abstract

Dopamine has been shown to influence blood pressure by regulating renal sodium excretion through direct interaction with the dopamine receptors, especially with the Dopamine D1 receptor (DRD1). To better understand the role of polymorphisms in those effects, we investigated the association between two polymorphic sites in the DRD1 promoter region (A-48G, G-94A) and essential hypertension in the Turkish population. The DRD1 variants were genotyped by restriction fragment length polymorphism (RFLP) analysis. A total of 205 unrelated individuals were enrolled in the study. We found that genotype distributions and allele frequencies of the control and hypertensive subjects were very similar and did not show any significant difference with respect to blood pressure (BP) and hypertension. Contribution of the gene variances in BP or hypertension by sex differences and dependence on body mass index (BMI) were also evaluated. Distribution of genotypes and allele frequencies were found to be in line with previous reports. However, increments detected in hypertensive subjects were far from being statistically significant.

摘要

多巴胺通过与多巴胺受体(尤其是多巴胺 D1 受体 [DRD1])的直接相互作用,调节肾脏钠排泄,从而影响血压。为了更好地理解这些影响中多态性的作用,我们研究了土耳其人群中 DRD1 启动子区域(A-48G、G-94A)两个多态性位点与原发性高血压之间的关联。通过限制性片段长度多态性(RFLP)分析对 DRD1 变体进行了基因分型。共有 205 名无血缘关系的个体参与了这项研究。我们发现,对照组和高血压组的基因型分布和等位基因频率非常相似,与血压(BP)和高血压均无显著差异。还评估了性别差异和对体重指数(BMI)的依赖性对 BP 或高血压中基因方差的贡献。基因型和等位基因频率的分布与先前的报告一致。然而,在高血压组中检测到的增量远没有统计学意义。

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