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mTOR 抑制剂依维莫司可降低原发性醛固酮增多症患者的血容量过多。

The mTOR-inhibitor everolimus reduces hypervolemia in patients with primary aldosteronism.

机构信息

Department of Endocrinology, Diabetes and Metabolism, University Hospital Basel, Basel, Switzerland -

Center for Physical Activity Research, Rigshospitalet, Copenhagen, Denmark -

出版信息

Minerva Endocrinol (Torino). 2024 Jun;49(2):150-157. doi: 10.23736/S2724-6507.21.03382-0. Epub 2021 Apr 1.

Abstract

BACKGROUND

We recently showed in a proof-of-concept study that treating individuals with primary aldosteronism with the mTOR-inhibitor everolimus decreases home blood pressure and renin suppression overall, and markedly reduces aldosterone levels in a subset of individuals. Based on these findings, the question arose whether the effects of everolimus were also mediated via aldosterone-independent mechanisms. Here, we undertook an exploratory, secondary analysis of above-mentioned study to comprehensively investigate how everolimus impacted the hemodynamic status of the study participants, which in turn could elucidate these mechanisms.

METHODS

Hemodynamic parameters were measured in study participants with primary aldosteronism at baseline, after treatment with everolimus 0.75 mg orally twice daily for 2 weeks and after a 2-week wash-out. Of the 14 participants, 10 participants had complete data sets for peripheral and central blood pressure, heart rate and pulse wave velocity, and 7 participants had complete data sets for cardiac index, inotropic state index, left stroke work index and stroke systemic vascular resistance index that could be analyzed. Parameters were acquired by brachial oscillometry (Mobil-o-graph PWA) and thoracic electrical bioimpedance (HOTMAN System).

RESULTS

After treatment with everolimus, peripheral (P=0.049) and central (P=0.037) diastolic blood pressure, as well as hypervolemia (P=0.008) were significantly decreased. Likewise, peripheral (P=0.073) and central systolic blood pressure (P=0.166) trended downwards.

CONCLUSIONS

Everolimus lowers central and peripheral blood pressure in individuals with primary aldosteronism, possibly by decreasing primary aldosteronism-induced hypervolemia and preload.

摘要

背景

我们最近在一项概念验证研究中表明,用 mTOR 抑制剂依维莫司治疗原发性醛固酮增多症患者,总体上降低了家庭血压和肾素抑制,并且在一部分患者中明显降低了醛固酮水平。基于这些发现,人们不禁产生疑问,依维莫司的作用是否也通过醛固酮非依赖性机制介导。在这里,我们对上述研究进行了探索性的二次分析,全面研究了依维莫司如何影响研究参与者的血液动力学状态,这反过来又可以阐明这些机制。

方法

在原发性醛固酮增多症患者中,在基线时、口服依维莫司 0.75mg 每天两次治疗 2 周后和 2 周洗脱期后测量血液动力学参数。在 14 名参与者中,有 10 名参与者有外周和中心血压、心率和脉搏波速度的完整数据集,有 7 名参与者有心脏指数、变力状态指数、左心搏做功指数和系统性血管阻力指数的完整数据集,这些数据可进行分析。参数通过臂动脉振荡测量法(Mobil-o-graph PWA)和胸部电生物阻抗(HOTMAN 系统)获得。

结果

依维莫司治疗后,外周(P=0.049)和中心(P=0.037)舒张血压以及血容量过多(P=0.008)显著降低。同样,外周(P=0.073)和中心收缩压(P=0.166)也呈下降趋势。

结论

依维莫司降低原发性醛固酮增多症患者的中心和外周血压,可能通过降低原发性醛固酮增多症引起的血容量过多和前负荷。

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