Veglio F, Morello F, Rabbia F, Leotta G, Mulatero P
Hypertension Unit, Department of Medicine and Experimental Oncology, S. Vito Hospital, University of Turin, Turin, Italy.
Minerva Med. 2003 Aug;94(4):259-65.
Primary aldosteronism is the most common form of secondary hypertension. The use of aldosterone/plasma renin activity ratio (ARR) as a screening test has elevated its prevalence up to 10% of hypertensive patients. Idiopathic bilateral adrenal hyperplasia and aldosterone-producing adrenal adenoma are the leading causes of primary aldosteronism. Most patients with this conditions are normokalemic and clinically undistinguishable from essential hypertensives. However, they suffer from anticipated and more severe target organ damage than other hypertensives. Thus, being primary aldosteronism a common, specifically treatable and sometimes surgically cured form of hypertension, a prompt diagnosis is necessary and cannot be overlooked. The measurement of ambulatory ARR represents the screening test and should be performed in the majority of hypertensive patients. ARR higher than a set cutoff suggests the need of a confirmatory test for primary aldosteronism, such as intravenous saline load or fludrocortisone suppression test. If inability to suppress aldosterone is demonstrated, the disease is confirmed. The subtype evaluation is based on adrenal imaging (CT scan) and selective adrenal venous sampling. The latter is the gold standard for the diagnosis of a lateralized aldosterone secretion, as typically observed in aldosterone-producing adenomas. Microadenomas are frequently overlooked by adrenal image. If lateralization is confirmed, unilateral adrenalectomy is the reasonable therapeutic option, leading to a significant reduction of blood pressure, if not normotension. If bilateral aldosterone excess is demonstrated, an aldosterone receptor antagonist should be administered. This article reviews and discusses the new data about prevalence, diagnosis and treatment of primary aldosteronism.
原发性醛固酮增多症是继发性高血压最常见的形式。使用醛固酮/血浆肾素活性比值(ARR)作为筛查试验,已将其在高血压患者中的患病率提高到了10%。特发性双侧肾上腺增生和醛固酮分泌性腺瘤是原发性醛固酮增多症的主要病因。大多数患有这种疾病的患者血钾正常,临床上与原发性高血压患者难以区分。然而,他们比其他高血压患者更容易出现预期的和更严重的靶器官损害。因此,鉴于原发性醛固酮增多症是一种常见的、可特异性治疗且有时可通过手术治愈的高血压形式,必须及时诊断,不容忽视。动态ARR的测量是筛查试验,应在大多数高血压患者中进行。高于设定临界值的ARR提示需要进行原发性醛固酮增多症的确诊试验,如静脉盐水负荷试验或氟氢可的松抑制试验。如果证实醛固酮不能被抑制,则可确诊该病。亚型评估基于肾上腺成像(CT扫描)和选择性肾上腺静脉采血。后者是诊断单侧醛固酮分泌的金标准,如在醛固酮分泌性腺瘤中通常所见。微腺瘤常被肾上腺成像漏诊。如果证实为单侧分泌,单侧肾上腺切除术是合理的治疗选择,即使不能使血压恢复正常,也可显著降低血压。如果证实双侧醛固酮分泌过多,则应给予醛固酮受体拮抗剂。本文回顾并讨论了有关原发性醛固酮增多症患病率、诊断和治疗的新数据。