首页> 外文期刊>Pharmacogenetics and genomics >Lack of association between polymorphisms in STK39, a putative thiazide response gene, and blood pressure response to hydrochlorothiazide.
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Lack of association between polymorphisms in STK39, a putative thiazide response gene, and blood pressure response to hydrochlorothiazide.

机译:推定的噻嗪类应答基因STK39中的多态性与对氢氯噻嗪的血压应答之间缺乏关联。

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摘要

STK39 was earlier implicated as a hypertension susceptibility gene and is thought to be involved in the control of Na-Cl co-transporter activity. STK39 has been implicated as a putative thiazide diuretic response gene, as Na-Cl co-transporter activity is inhibited by thiazides. Thus, we aimed to determine whether STK39 is a thiazide response gene. One hundred and ninety-five 'good' and 194 'poor' responders to hydrochlorothiazide (HCTZ) were genotyped for approximately 100 single nucleotide polymorphisms (SNPs) within 5000 bases of STK39. SNPs meeting criteria for advancement to replication analysis (P<0.01), along with those earlier associated with hypertension, were then analyzed in a second population of 201 HCTZ-treated hypertensives. Two SNPs passed screening and were further analyzed. However, neither these, nor earlier implicated SNPs met criteria for significant association with blood pressure response to HCTZ. These data suggest that common variants in STK39 likely do not have a clinically relevant role in blood pressure response to HCTZ in hypertensives.
机译:STK39以前被认为是高血压易感基因,被认为与Na-Cl共转运蛋白活性的控制有关。 STK39被认为是推定的噻嗪类利尿剂应答基因,因为噻嗪类抑制了Na-Cl共转运蛋白活性。因此,我们旨在确定STK39是否为噻嗪类应答基因。对STK39的5000个碱基内的大约100个单核苷酸多态性(SNP),对195对氢氯噻嗪(HCTZ)的“好”和194个“差”的应答者进行了基因分型。然后在第二批接受HCTZ治疗的高血压人群中分析了符合复制分析标准的SNP(P <0.01),以及较早与高血压相关的SNP。两个SNP通过了筛选,并进行了进一步分析。但是,这些以及早期牵连的SNP均未达到与HCTZ血压反应显着相关的标准。这些数据表明,STK39的常见变异在高血压中对HCTZ的血压反应中可能没有临床相关的作用。

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