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一项评估他汀类药物使用对降低醛固酮水平影响的临床试验。

A clinical trial to evaluate the effect of statin use on lowering aldosterone levels.

机构信息

Division of Endocrinology, Diabetes, and Hypertension, Brigham and Women's Hospital and Harvard Medical School, 221 Longwood Ave, Boston, MA, 02115, USA.

出版信息

BMC Endocr Disord. 2020 Jul 14;20(1):105. doi: 10.1186/s12902-020-00587-4.

Abstract

BACKGROUND

Statins are the first-line pharmaceutical agent in the management of hypercholesterolemia and cardiovascular (CV) risk reduction, and the most commonly prescribed class of drugs worldwide. Studies describing CV risk reduction independent of LDL-cholesterol lowering have evoked an interest in the pleiotropic mechanisms of statins' benefits. We recently demonstrated that administration of statins in animal models lowers aldosterone levels and observed an association between statin use and reduced aldosterone levels in two human cohorts, with lipophilic statins displaying a greater effect than hydrophilic statins. Therefore, we designed a randomized, placebo-controlled, double-blinded intervention study to assess whether statin treatment lowers aldosterone in a type-dependent manner in humans, with simvastatin (lipophilic) showing a greater effect than pravastatin (hydrophilic).

METHODS/DESIGN: One hundred five healthy participants will be recruited from the general population to enroll in a 12-week, randomized, placebo-controlled, double-blinded, 3-arm clinical trial. Ninety participants are anticipated to complete the protocol. After baseline assessment of aldosterone levels, participants will be randomized to daily simvastatin, pravastatin, or placebo. Aldosterone levels will be assessed after 2 days on study drug and again after 6 weeks and 12 weeks on study drug. Prior to each aldosterone assessment, participants will consume an isocaloric sodium and potassium-controlled run-in diet for 5 days. Assessments will occur on an inpatient research unit to control for diurnal, fasting, and posture conditions. The primary outcome will compare 12-week angiotensin II-stimulated serum aldosterone by study drug. Secondary outcomes will compare baseline and 12-week 24-h urine aldosterone by study drug.

DISCUSSION

Results from this rigorous study design should provide strong support that statins lower aldosterone levels in humans. These results may explain some of the beneficial effects of statins that are not attributed to the LDL-lowering effect of this important class of medications. Results would demonstrate that statin lipophilicity is an important attribute in lowering aldosterone levels. The outcomes of this program will have implications for the design of studies involving statin medications, as well as for the differential use of classes of statins.

TRIAL REGISTRATION

ClinicalTrials.gov; NCT02871687 ; First Posted August 18, 2016.

摘要

背景

他汀类药物是治疗高胆固醇血症和降低心血管(CV)风险的一线药物,也是全球最常用的药物类别。描述他汀类药物降低心血管风险与降低 LDL 胆固醇无关的研究引起了人们对他汀类药物多效机制的兴趣。我们最近在动物模型中证明,他汀类药物的给药可降低醛固酮水平,并在两个人类队列中观察到他汀类药物使用与降低醛固酮水平之间的关联,亲脂性他汀类药物的作用大于亲水性他汀类药物。因此,我们设计了一项随机、安慰剂对照、双盲干预研究,以评估他汀类药物治疗是否以依赖于类型的方式降低人类的醛固酮水平,辛伐他汀(亲脂性)的作用大于普伐他汀(亲水性)。

方法/设计:将从普通人群中招募 105 名健康参与者入组一项为期 12 周的随机、安慰剂对照、双盲、三臂临床试验。预计 90 名参与者将完成方案。在基线评估醛固酮水平后,参与者将随机接受每日辛伐他汀、普伐他汀或安慰剂治疗。在开始研究药物治疗后 2 天、6 周和 12 周后评估醛固酮水平。在每次醛固酮评估之前,参与者将在 5 天内接受等热量钠钾控制的预备饮食。评估将在住院研究单位进行,以控制昼夜、空腹和体位条件。主要结局将比较研究药物治疗 12 周后血管紧张素 II 刺激的血清醛固酮。次要结局将比较研究药物治疗的基线和 12 周 24 小时尿醛固酮。

讨论

这项严格的研究设计的结果应该为他汀类药物降低人类醛固酮水平提供强有力的支持。这些结果可能解释了他汀类药物的一些有益作用,这些作用不能归因于这种重要药物类别的 LDL 降低作用。结果将表明,他汀类药物的亲脂性是降低醛固酮水平的一个重要属性。该项目的结果将对涉及他汀类药物的研究设计以及他汀类药物类别的差异使用产生影响。

试验注册

ClinicalTrials.gov;NCT02871687;首次报告 2016 年 8 月 18 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bced/7362429/a89b2ee2f157/12902_2020_587_Fig1_HTML.jpg

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