Ardhanari Sivakumar, Kannuswamy Rohini, Chaudhary Kunal, Lockette Warren, Whaley-Connell Adam
Department of Medicine, University of Missouri-Columbia School of Medicine, Columbia, MO; Division of Cardiovascular Medicine, University of Missouri-Columbia School of Medicine, Columbia, MO; Department of Pathology and Anatomical Sciences, University of Missouri, Columbia, MO; Division of Nephrology and Hypertension, University of Missouri-Columbia School of Medicine, Columbia, MO; Research Service, Harry S. Truman Memorial Veterans Hospital, Columbia, MO; and Division of Endocrinology and Metabolism, University of Missouri-Columbia School of Medicine, Columbia, MO.
Department of Medicine, University of Missouri-Columbia School of Medicine, Columbia, MO; Division of Cardiovascular Medicine, University of Missouri-Columbia School of Medicine, Columbia, MO; Department of Pathology and Anatomical Sciences, University of Missouri, Columbia, MO; Division of Nephrology and Hypertension, University of Missouri-Columbia School of Medicine, Columbia, MO; Research Service, Harry S. Truman Memorial Veterans Hospital, Columbia, MO; and Division of Endocrinology and Metabolism, University of Missouri-Columbia School of Medicine, Columbia, MO.
Adv Chronic Kidney Dis. 2015 May;22(3):185-95. doi: 10.1053/j.ackd.2015.03.002.
The mineralocorticoid aldosterone is a key hormone in the regulation of plasma volume and blood pressure in man. Excessive levels of this mineralocorticoid have been shown to mediate metabolic disorders and end-organ damage more than what can be attributed to its effects on blood pressure alone. Inappropriate excess levels of aldosterone contribute significantly to the cardiorenal metabolic syndrome and target organ injury that include atherosclerosis, myocardial hypertrophy, fibrosis, heart failure, and kidney disease. The importance of understanding the role of excess mineralocorticoid hormones such as aldosterone in resistant hypertension and in those with secondary hypertension should be visited. Primary aldosteronism is one of the commonly identified causes of hypertension and is treatable and/or potentially curable. We intend to review the management of mineralocorticoid-induced hypertension in the adult population along with other disease entities that mimic primary aldosteronism.
盐皮质激素醛固酮是人体调节血容量和血压的关键激素。已表明,这种盐皮质激素水平过高所介导的代谢紊乱和终末器官损害,不仅仅是其对血压的影响所能解释的。醛固酮水平异常过高是导致心肾代谢综合征和靶器官损伤的重要因素,这些损伤包括动脉粥样硬化、心肌肥大、纤维化、心力衰竭和肾脏疾病。有必要深入了解过量的盐皮质激素如醛固酮在顽固性高血压和继发性高血压患者中的作用。原发性醛固酮增多症是常见的高血压病因之一,且可治疗和/或潜在可治愈。我们打算综述成年人群中盐皮质激素诱导的高血压以及其他类似原发性醛固酮增多症的疾病实体的管理。