Salt, aldosterone and hypertension

被引:26
作者
Pimenta, E. [2 ,3 ,4 ]
Gordon, R. D. [2 ]
Stowasser, M. [1 ,2 ,3 ,4 ]
机构
[1] Univ Queensland, Princess Alexandra Hosp, Hypertens Unit, Endocrine Hypertens Res Ctr,Sch Med, Brisbane, Qld 4102, Australia
[2] Univ Queensland, Greenslopes Hosp, Sch Med, Endocrine Hypertens Res Ctr, Brisbane, Qld 4102, Australia
[3] Univ Queensland, Princess Alexandra Hosp, Clin Ctr Res Excellence Cardiovasc Dis & Met Diso, Sch Med, Brisbane, Qld 4102, Australia
[4] Univ Queensland, Greenslopes Hosp, Clin Ctr Res Excellence Cardiovasc Dis & Metab Di, Sch Med, Brisbane, Qld 4102, Australia
关键词
hypertension; salt; aldosterone; RESISTANT HYPERTENSION; BLOOD-PRESSURE; MYOCARDIAL FIBROSIS; DIETARY-SODIUM; HEART-FAILURE; URINARY SODIUM; DIAGNOSIS; EXCRETION; OUTCOMES; HYPERALDOSTERONISM;
D O I
10.1038/jhh.2012.27
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Clinical studies have shown that aldosterone and salt are independently related to hypertension, cardiovascular morbidity and mortality. More recently, studies in humans have demonstrated that, similarly to animals, endogenous aldosterone and dietary salt intake have not only separate, but also combined effects to accelerate target-organ deterioration. The aldosterone-salt interaction has important clinical implications, because combined effects of both can be minimized, if not avoided, by reducing salt intake. This interaction could also be interrupted by blocking the effects of aldosterone, with use of mineralocorticoid receptor antagonists, or by reducing aldosterone effects by adrenalectomy, in patients with aldosterone producing adenoma. Furthermore, aldosterone reduction or blockade may reduce salt appetite. Journal of Human Hypertension (2013) 27, 1-6; doi:10.1038/jhh.2012.27; published online 12 July 2012
引用
收藏
页码:1 / 6
页数:6
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