Williams Gordon H
Endocrinology, Diabetes and Hypertension Division, Brigham and Women's Hospital, Harvard Medical School, 221 Longwood Avenue, RFB-2, Boston, MA 02115, USA.
Mol Cell Endocrinol. 2004 Mar 31;217(1-2):41-4. doi: 10.1016/j.mce.2003.10.007.
Defining the genetic basis of essential hypertension is most informative when the blood pressure regulation is correlated with physiologic mechanisms, e.g., responses of the renin-angiotensin aldosterone system (RAAS) in hypertensive subjects. The aldosterone response to angiotensin II (Ang II) on a low salt diet is influenced by gender, plasma renin activity, and most significantly, familial resemblance, but only in males and in post-menopausal females. There is familial aggregation of low-renin hypertension, no association with candidate genes of the RAAS, but, a highly significant association with polymorphisms in the alpha-adducin gene. Finally, angiotensinogen (AGT) genotype effects renal and adrenal responses to Ang II in patients with hypertension. These results strongly suggest that in contrast to population-based studies that use hypertension as the phenotype, classifying patients by the variability in physiologic, mechanistic traits enhances the probability of identifying the genetic factors influencing a rise in blood pressure.
当血压调节与生理机制相关时,例如高血压患者肾素-血管紧张素-醛固酮系统(RAAS)的反应,确定原发性高血压的遗传基础最具参考价值。低盐饮食时醛固酮对血管紧张素II(Ang II)的反应受性别、血浆肾素活性影响,最重要的是受家族相似性影响,但仅在男性和绝经后女性中如此。低肾素性高血压存在家族聚集性,与RAAS的候选基因无关联,但与α-加ducin基因的多态性有高度显著关联。最后,血管紧张素原(AGT)基因型影响高血压患者肾脏和肾上腺对Ang II的反应。这些结果强烈表明,与以高血压为表型的基于人群的研究不同,根据生理、机制特征的变异性对患者进行分类可提高识别影响血压升高的遗传因素的可能性。