He Xin, Modi Zubin, Else Tobias
Division of Metabolism, Endocrinology, and Diabetes, University of Michigan, Ann Arbor, MI, USA.
Division of Pediatric Nephrology, Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA.
Gland Surg. 2020 Feb;9(1):150-158. doi: 10.21037/gs.2019.11.20.
Secondary hypertension is a common condition with a broad differential diagnosis. Identification of the true cause of hypertension can be critical for guiding appropriate management. Here, we review hereditary conditions underlying the most common cause of secondary hypertension, primary aldosteronism, as well as other disorders impacting various levels of mineralocorticoid action. Recently, several pathogenic variants of ion channels have been described as etiologies of familial aldosteronism. Defects in steroid hormone synthesis cause hypertension in 11β-hydroxylase deficiency and 17α-hydroxylase deficiency, two types of congenital adrenal hyperplasia. Inappropriate activation of mineralocorticoid receptors underlies the syndrome of apparent mineralocorticoid excess and constitutive activation of the mineralocorticoid receptor. Finally, Liddle syndrome and pseudohypoaldosteronism type 2 are disorders impacting the function of renal sodium channels, the endpoint of mineralocorticoid action. We discuss the pathophysiology, clinical presentation, diagnosis and management of these low renin hypertension states that ultimately result in apparent excess mineralocorticoid activity.
继发性高血压是一种常见疾病,鉴别诊断范围广泛。确定高血压的真正病因对于指导恰当的治疗至关重要。在此,我们回顾继发性高血压最常见病因——原发性醛固酮增多症的遗传状况,以及影响盐皮质激素作用各个层面的其他病症。最近,已将几种离子通道的致病变异描述为家族性醛固酮增多症的病因。类固醇激素合成缺陷在11β-羟化酶缺乏症和17α-羟化酶缺乏症(两种先天性肾上腺增生类型)中导致高血压。盐皮质激素受体的不适当激活是表观盐皮质激素过多综合征和盐皮质激素受体组成性激活的基础。最后,利德尔综合征和2型假性醛固酮减少症是影响肾钠通道功能(盐皮质激素作用的终点)的病症。我们讨论这些低肾素性高血压状态的病理生理学、临床表现、诊断和治疗,这些状态最终导致明显的盐皮质激素活性过剩。