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原发性醛固酮增多症:一种常见且可治愈的高血压类型。

Primary aldosteronism: A common and curable form of hypertension.

作者信息

Young W F

机构信息

Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.

出版信息

Cardiol Rev. 1999 Jul-Aug;7(4):207-14.

Abstract

Since its initial description in 1955, primary aldosteronism was thought to be a rare cause of hypertension. However, with improved screening methodologies, it appears that primary aldosteronism is the most common form of secondary hypertension. Diagnosis of this disorder results in either the cure of hypertension or targeted pharmacotherapy. In addition, recent evidence suggests that aldosterone excess may have specific cardiotoxicity that is reversible with treatment. Patients with hypertension and hypokalemia and most patients with treatment-resistant hypertension should undergo screening for primary aldosteronism. A random and ambulatory ratio of plasma aldosterone concentration (ng/dl) to plasma renin activity (ng/ml per hour) >20 and a plasma aldosterone concentration >15 ng/dl is a positive screen for primary aldosteronism. A plasma aldosterone concentration/plasma renin activity ratio >20 alone is not diagnostic of primary aldosteronism; primary aldosteronism must be confirmed by demonstrating inappropriate aldosterone secretion with either the intravenous saline suppression test or measurement of 24-hour urinary aldosterone while on a high-sodium diet. The 2 major subtypes of primary aldosteronism are unilateral aldosterone-producing adenoma and bilateral idiopathic hyperplasia. Patients with aldosterone-producing adenoma are usually treated with unilateral adrenalectomy, and patients with idiopathic hyperplasia are treated medically. The subtype evaluation may require one or more tests, the first of which is imaging the adrenals with computed tomography (CT). When CT reveals a solitary unilateral macroadenoma (>1 centimeter) and normal contralateral adrenal morphology in a patient with primary aldosteronism, unilateral laparoscopic adrenalectomy is a reasonable therapeutic option. However, in many cases, CT imaging may reveal normal-appearing adrenals or ambiguous findings. Adrenal venous sampling helps solve these clinical dilemmas.

摘要

自1955年首次被描述以来,原发性醛固酮增多症一直被认为是高血压的罕见病因。然而,随着筛查方法的改进,原发性醛固酮增多症似乎是继发性高血压最常见的形式。对这种疾病的诊断要么能治愈高血压,要么能进行有针对性的药物治疗。此外,最近的证据表明,醛固酮过量可能具有特定的心脏毒性,治疗后可逆转。高血压合并低钾血症的患者以及大多数顽固性高血压患者应接受原发性醛固酮增多症的筛查。血浆醛固酮浓度(ng/dl)与血浆肾素活性(ng/ml每小时)的随机和动态比值>20且血浆醛固酮浓度>15 ng/dl是原发性醛固酮增多症的阳性筛查结果。仅血浆醛固酮浓度/血浆肾素活性比值>20并不能诊断原发性醛固酮增多症;必须通过静脉盐水抑制试验或在高钠饮食时测量24小时尿醛固酮来证明醛固酮分泌异常,才能确诊原发性醛固酮增多症。原发性醛固酮增多症的2种主要亚型是单侧醛固酮分泌腺瘤和双侧特发性增生。醛固酮分泌腺瘤患者通常接受单侧肾上腺切除术,特发性增生患者接受药物治疗。亚型评估可能需要一项或多项检查,首先是用计算机断层扫描(CT)对肾上腺进行成像。当CT显示原发性醛固酮增多症患者有孤立的单侧大腺瘤(>1厘米)且对侧肾上腺形态正常时,单侧腹腔镜肾上腺切除术是一种合理的治疗选择。然而,在许多情况下,CT成像可能显示肾上腺外观正常或结果不明确。肾上腺静脉采血有助于解决这些临床难题。

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