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首页> 外文期刊>Journal of hypertension >Bradykinin B2 receptor gene (-58T/C) polymorphism influences baroreflex sensitivity in never-treated hypertensive patients.
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Bradykinin B2 receptor gene (-58T/C) polymorphism influences baroreflex sensitivity in never-treated hypertensive patients.

机译:缓激肽B2受体基因(-58T / C)多态性影响从未治疗的高血压患者的压力反射敏感性。

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摘要

BACKGROUND: Most evidence currently favours a fundamental role of the autonomic nervous system in the pathogenesis of essential hypertension. Recent studies suggest that about 40% of baroreflex variation, an index of cardiac autonomic control, is influenced by genetic factors. METHODS AND RESULTS: The aim of this study was to investigate the effect of a common polymorphic variant of the bradykinin B2 receptor gene (B2R; -58T/C) on the autonomic regulation of baroreflex sensitivity (BRS) in 129 mild-moderate never-treated hypertensive patients. No significant differences were found for clinical and biochemical parameters among genotypes. BRS increased with the number of B2R T alleles. B2R genotype was a strong independent predictor of BRS, accounting for 12% of its variation. We suggest that a decrease in the transcription of the bradykinin B2R gene in the presence of the B2R -58C allele could reduce BRS via the diminished effect of bradykinin. CONCLUSIONS: B2R genotype can explain part of the BRS variation that is unaccounted for by simple anthropometric variables and common risk factors.
机译:背景:目前,大多数证据支持植物神经系统在原发性高血压发病中的基本作用。最近的研究表明,约40%的压力反射变化是心脏自主神经控制的指标,受遗传因素影响。方法和结果:本研究的目的是研究缓激肽B2受体基因(B2R; -58T / C)的常见多态性变异体对129轻度中度永不应激的压力反射敏感性(BRS)的自主调节的影响。治疗高血压患者。基因型之间在临床和生化指标上没有发现显着差异。 BRS随B2R T等位基因数目的增加而增加。 B2R基因型是BRS的强烈独立预测因子,占其变异的12%。我们建议在存在B2R -58C等位基因的情况下,缓激肽B2R基因转录的减少可能通过缓激肽的减弱作用而降低BRS。结论:B2R基因型可以解释部分BRS变异,这是简单的人体测量学变量和常见危险因素所无法解释的。

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