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低肾素性高血压综合征:“去伪存真”

The syndromes of low-renin hypertension: "separating the wheat from the chaff".

作者信息

Kater Claudio E, Biglieri Edward G

机构信息

Adrenal and Hypertension Unit, Division of Endocrinology, Department of Medicine, Universidade Federal de São Paulo, São Paulo, SP.

出版信息

Arq Bras Endocrinol Metabol. 2004 Oct;48(5):674-81. doi: 10.1590/s0004-27302004000500013. Epub 2005 Mar 7.

Abstract

Primary aldosteronism (PA) is characterized by hypertension and suppressed renin activity with or without hypokalemia and comprises the aldosterone-producing adenoma (APA) and bilateral adrenal hyperplasia or idiopatic hyperaldosteronism (IHA). In recent series employing the aldosterone (aldo, ng/dL):renin (ng/mL.h) ratio (ARR) for screening, prevalence of PA among hypertensives soars to 8-20%; current predominance of IHA (>80%) over APA suggests the inclusion of former low-renin essential hypertensives (LREH), in whom plasma aldo can be reduced by suppressive maneuvers. We evaluated the test characteristics of the ARR obtained retrospectively from 127 patients with PA (81 APA; 46 IHA) and 55 with EH (30 LREH; 25 NREH) studied from 1975 to 1990. Using the combined ROC-defined cutoffs of 27 for the ARR and 12ng/dL for aldo, we obtained 89.8% sensitivity (Ss) and 98.2% specificity (Sp) in discriminating PA from EH: all APA and 72% of the IHA patients had values above these limits, but only one (3%) with LREH. Among the 46 IHA patients, 10 (21.7%) had ARR <27, four of whom with aldo <12ng/dL, virtually indistinguishable from LREH. Use of higher cutoff values (ARR > or =100; aldo > or =20) may attain 84%Ss and 82.6%Sp in separating APA from IHA. Because IHA and LREH ("the chaff") may be spectrum stages from the same disease, definite discrimination between these entities seems immaterial. However, precise identification of the APA ("the wheat") is critical, since it is the only surgically curable form of PA. Thus, while patients who may harbor an APA must be thoroughly investigated and surgically treated, non-tumoral disease (IHA and LREH) may be best treated with an aldo-receptor antagonist that will also prevent the aldo-mediated inflammatory effects involved in myocardial fibrosis and abnormal cardiac remodeling.

摘要

原发性醛固酮增多症(PA)的特征为高血压和肾素活性受抑制,伴或不伴低钾血症,包括醛固酮瘤(APA)以及双侧肾上腺增生或特发性醛固酮增多症(IHA)。在近期采用醛固酮(aldo,ng/dL):肾素(ng/mL·h)比值(ARR)进行筛查的系列研究中,高血压患者中PA的患病率飙升至8% - 20%;目前IHA(>80%)比APA更为常见,这表明应将前者纳入低肾素原发性高血压(LREH),此类患者的血浆醛固酮可通过抑制措施降低。我们评估了从1975年至1990年研究的127例PA患者(81例APA;46例IHA)和55例原发性高血压(EH)患者(30例LREH;25例非LREH)中回顾性获得的ARR的检测特征。使用联合ROC定义的ARR截断值27和醛固酮截断值12ng/dL,我们在区分PA和EH时获得了89.8%的灵敏度(Ss)和98.2%的特异度(Sp):所有APA患者和72%的IHA患者的值高于这些限值,但LREH患者中只有1例(3%)高于此值。在46例IHA患者中,10例(21.7%)的ARR <27,其中4例醛固酮<12ng/dL,几乎与LREH无法区分。使用更高的截断值(ARR≥100;醛固酮≥20)在区分APA和IHA时可达到84%的Ss和82.6%的Sp。由于IHA和LREH(“谷壳”)可能是同一疾病的不同阶段,明确区分这些实体似乎并不重要。然而,精确识别APA(“麦粒”)至关重要,因为它是PA唯一可通过手术治愈的形式。因此,虽然可能患有APA的患者必须进行全面检查并接受手术治疗,但非肿瘤性疾病(IHA和LREH)可能最好用醛固酮受体拮抗剂治疗,这也将预防醛固酮介导的涉及心肌纤维化和异常心脏重塑的炎症效应。

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