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13 年间原发性醛固酮增多症临床表现亚型特异性变化趋势。

Subtype-specific trends in the clinical picture of primary aldosteronism over a 13-year period.

机构信息

Department of Endocrinology, Metabolism and Nephrology, School of Medicine, Keio University, Tokyo.

Center for Diabetes, Endocrinology and Metabolism, Shizuoka General Hospital, Shizuoka.

出版信息

J Hypertens. 2021 Nov 1;39(11):2325-2332. doi: 10.1097/HJH.0000000000002924.

DOI:
10.1097/HJH.0000000000002924
PMID:34224538
Abstract

OBJECTIVE

Primary aldosteronism has two main clinically and biologically distinct subtypes: unilateral aldosterone-producing adenoma (APA) and bilateral adrenal hyperplasia (BAH). We aimed to evaluate the changes of each subtype's clinical characteristics over a 13-year period.

METHODS

This retrospective study involved time-trend analyses to identify changes in the clinical features of APA and BAH at diagnosis (2006-2018). A nationwide database from 41 Japanese referral centers was searched, which identified 2804 primary aldosteronism patients with complete baseline information and adrenal venous sampling (AVS) data.

RESULTS

The proportion of patients with APA decreased from 51% in 2006-2009 to 22% in 2016-2018. Among the 1634 patients with BAH, trend analyses revealed decreases in hypertension duration (median 7--3 years; P < 0.01) and hypokalemia prevalence (18--11%; P < 0.01). However, among the 952 patients with APA, there were no significant changes in hypertension duration (median 8 years) and hypokalemia prevalence (overall 70%). Furthermore, the APA group had a trend towards increased use of multiple hypertensive drugs at diagnosis (30--43%; P < 0.01). When subtypes were reclassified according to the precosyntropin stimulation AVS data, APA patients tended to be diagnosed earlier and at milder forms, consistent with the trend in overall primary aldosteronism patients.

CONCLUSION

During 2006-2018, we identified marked subtype-specific trends in the clinical findings at the diagnosis of primary aldosteronism. Our results suggested that the emphasis on the implementing cosyntropin stimulation during AVS might lead to under-identification of APA, especially in patients with mild or early cases.

摘要

目的

原发性醛固酮增多症有两种主要的临床和生物学上明显不同的亚型:单侧醛固酮分泌腺瘤(APA)和双侧肾上腺增生(BAH)。我们旨在评估在 13 年期间每个亚型的临床特征变化。

方法

本回顾性研究进行了时间趋势分析,以确定 2006-2018 年诊断时 APA 和 BAH 的临床特征变化。从 41 家日本转诊中心的全国性数据库中搜索,确定了 2804 例原发性醛固酮增多症患者,这些患者具有完整的基线信息和肾上腺静脉采样(AVS)数据。

结果

APA 患者的比例从 2006-2009 年的 51%降至 2016-2018 年的 22%。在 1634 例 BAH 患者中,趋势分析显示高血压持续时间(中位数 7-3 年;P<0.01)和低钾血症发生率(18-11%;P<0.01)降低。然而,在 952 例 APA 患者中,高血压持续时间(中位数 8 年)和低钾血症发生率(总体 70%)无显著变化。此外,APA 组在诊断时使用多种降压药物的趋势增加(30-43%;P<0.01)。当根据预皮质激素刺激 AVS 数据重新分类亚型时,APA 患者倾向于更早诊断和更轻的形式,与原发性醛固酮增多症患者的总体趋势一致。

结论

在 2006-2018 年期间,我们发现原发性醛固酮增多症诊断时临床发现的明显的亚型特异性趋势。我们的结果表明,在 AVS 期间强调使用皮质激素刺激可能导致 APA 识别不足,尤其是在轻度或早期病例中。

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