Stowasser Michael
Endocrine Hypertension Research Centre, Greenslopes and Princess Alexandra Hospitals, University of Queensland School of Medicine, Ipswich Road, Woolloongabba, Queensland, 4102, Australia,
Curr Hypertens Rep. 2014 Jul;16(7):439. doi: 10.1007/s11906-014-0439-7.
Among patients with resistant hypertension, primary aldosteronism (PA) is worth detecting as it appears to be particularly common in this cohort. It is associated with excessive cardiovascular morbidity in relation to the degree of hypertension and reduced quality of life, both of which can be abrogated with specific surgical or medical treatment. Knowledge concerning factors (including medications) which can influence the results of screening by aldosterone/renin ratio (ARR) testing is expanding, and is important to appreciate, particularly in patients with resistant hypertension, in whom the need for multiple medications can render interpretation challenging. Advances in approaches to confirmatory testing, subtype differentiation and assay methodology are helping to improve feasibility and reliability of the diagnostic workup for PA and new treatment approaches are emerging. Major developments in understanding the genetic bases for PA hold promise towards further improvements and options in diagnosis and therapy.
在顽固性高血压患者中,原发性醛固酮增多症(PA)值得检测,因为它在这一群体中似乎特别常见。PA与高血压程度相关的心血管发病率过高以及生活质量下降有关,而这两者都可以通过特定的手术或药物治疗得到改善。关于可能影响醛固酮/肾素比值(ARR)检测筛查结果的因素(包括药物)的知识正在不断扩展,这一点很重要,尤其是在顽固性高血压患者中,因为多种药物治疗的需求可能会使结果解读具有挑战性。在确诊检测、亚型分化和检测方法方面的进展有助于提高PA诊断检查的可行性和可靠性,新的治疗方法也正在出现。对PA遗传基础的深入理解取得的重大进展有望进一步改善诊断和治疗并提供更多选择。