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汉族人群 CYP11B2 基因与原发性高血压的关联:基于单体型的病例对照研究。

Association of the human CYP11B2 gene and essential hypertension in southwest Han Chinese population: a haplotype-based case-control study.

机构信息

Human Genetics Center of Yunnan University, PR China.

出版信息

Clin Exp Hypertens. 2011;33(2):106-12. doi: 10.3109/10641963.2010.531835. Epub 2011 Jan 26.

Abstract

Aldosterone synthase produces aldosterone, which regulates electrolytes and thereby blood pressure (BP). The aldosterone-synthase gene (CYP11B2) has been regarded as a candidate gene for essential hypertension. To address this issue, we carried out a haplotype-based, case-control study to explore the association between a human CYP11B2 gene and essential hypertension (EH) in the southwest Han population of China (n = 1020 individuals). Four tag single-nucleotide polymorphisms (SNPs) (rs4536, rs4545, rs3097, and rs3802230) and the C-344T polymorphism, as well as the K173R polymorphism in the CYP11B2 gene, were genotyped using the PCR-RFLP method. Single-locus analysis showed that the C allele of rs3802230 was significantly more prevalent in the EH subjects as compared to control subjects, adjusted for covariates. Haplotype analysis showed that the haplotype AAGC constructed by the tag SNPs (rs4536, rs4545, rs3097, and rs3802230), which carried the susceptible rs3802230 C allele, significantly increased the risk of essential hypertension with an odds ratios equal to 3.56 (P = 0.0001). The present results indicated that the rs3802230 C allele might be a risk marker for essential hypertension and haplotype AAGC might confer high genetic susceptibility to essential hypertension in a southwest Han Chinese population.

摘要

醛固酮合酶产生醛固酮,调节电解质,从而调节血压(BP)。醛固酮合酶基因(CYP11B2)已被视为原发性高血压的候选基因。为了解决这个问题,我们进行了基于单体型的病例对照研究,以探讨中国西南汉族人群 CYP11B2 基因与原发性高血压(EH)之间的关联(n=1020 人)。使用 PCR-RFLP 方法对四个标签单核苷酸多态性(SNP)(rs4536、rs4545、rs3097 和 rs3802230)和 CYP11B2 基因的 C-344T 多态性以及 K173R 多态性进行了基因分型。单基因分析表明,与对照组相比,EH 患者 rs3802230 的 C 等位基因明显更为常见,调整了协变量。单体型分析表明,由标签 SNP(rs4536、rs4545、rs3097 和 rs3802230)构建的单体型 AAGC 携带易感 rs3802230 C 等位基因,显著增加了原发性高血压的风险,比值比等于 3.56(P=0.0001)。本研究结果表明,rs3802230 C 等位基因可能是原发性高血压的风险标志物,单体型 AAGC 可能在中国西南汉族人群中赋予原发性高血压的高遗传易感性。

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