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临床试验/NCT01319344
NCT01319344已完成3 期

Prospective and Open Label Study With Blind End Point Evaluation on the Effect of Mineralocorticoid Receptor Inhibition on Endothelial Function of the Micro- and Macrovasculature in Patients With Metabolic Syndrome

University of Erlangen-Nürnberg Medical School2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2010年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
42
试验地点
2
主要终点
Change of basal nitric oxide activity as assessed by change of retinal capillary flow (measured by Scanning Laser Doppler Flowmetry)

研究概览

简要总结

Patients with the metabolic syndrome (MetSyn) are at increased risk for cardiovascular mortality and morbidity.This increased cardiovascular risk is attributed to metabolic dysregulations like impaired glucose tolerance or diabetes mellitus and dyslipidemia, abdominal obesity and arterial hypertension, which promote oxidative stress and inflammation with consecutive endothelial dysfunction causing an atherogenic environment.

Aldosterone promoted end organ damage is mainly found in the cardiovascular system and the kidney. Inflammation and activation of different factors promotes fibroblast growth and matrix production resulting in myocardial fibrosis, vascular remodelling and renal fibrosis.

MetSyn and aldosterone are cardiovascular risk factors and it is of crucial importance to note that there is a connection between MetSyn and aldosterone. Other cross sectional studies show a direct correlation of aldosterone levels and impaired glucose metabolism in patients with and without the MetSyn. Taken together, aldosterone influences essential parameters of the MetSyn. Coincidentally parameters of the MetSyn are stimulus for an increased aldosterone synthesis, i.e. visceral adipocytes.

In large scale clinical trials - RALES, EPHESUS, 4E - inhibition of MR has proven to be beneficial in patients with congestive heart failure and post myocardial infarction and this result has been confirmed for diabetic patients, who are known to have an increased cardiovascular risk.

There is only very limited data on the impact of MR inhibition on metabolic, endocrine, and inflammatory parameters in patients with MetSyn, who have not yet suffered from cardiovascular events.

详细描述

Patients with the metabolic syndrome (MetSyn) are at increased risk for cardiovascular mortality and morbidity.

This increased cardiovascular risk is attributed to metabolic dysregulations like impaired glucose tolerance or diabetes mellitus and dyslipidemia, abdominal obesity and arterial hypertension, which promote oxidative stress and inflammation and together cause an atherogenic environment. MetSyn is now a well established cardiovascular risk factor and prevalence and incidence of MetSyn in the western world are constantly rising with 19.8 percent prevalence in Germany 4.

Aldosterone is predominantly synthesized in the adrenal glands. In addition, local aldosterone synthesis has been found in the heart and vasculature and aldosterone synthesis in adipocytes is discussed. Aldosterone exerts its effects via the mineralocorticoid receptor (MR). Besides the well described MR in the distal tubule of the kidney MR have also been detected in other organs such as the vasculature and a paracrine mode of action is discussed. Recently it has been described, that MR can be activated independent of aldosterone in hypertensive and obese rats 1. Aldosterone promoted end organ damage is mainly found in the cardiovascular system and the kidney. Inflammation and activation of different factors promotes fibroblast growth and matrix production resulting in myocardial fibrosis, vascular remodelling and renal fibrosis. Aldosterone appears to be involved in all steps of this process by synthesis of reactive oxygen species, induction of inflammation and growth factors like TGF-Beta and connective tissue growth factor. Taken together aldosterone - as the MetSyn- is an independent cardiovascular risk factor 5.

MetSyn and aldosterone are cardiovascular risk factors and it is of crucial importance to note that there is a connection between MetSyn and aldosterone. In clinical studies it was clearly demonstrated that Renin and Aldosterone in patients with MetSyn are elevated 6. Similar results have been obtained in animal studies where obesity induced arterial hypertension increased renin and aldosterone levels 7-9. In a cross sectional study with 397 participants the impact of aldosterone on the onset of arterial hypertension and MetSyn was analysed. In this study blood pressure was associated with aldosterone levels and aldosterone was correlated with waist circumference, insulin, HOMA index and an unfavourable lipid profile 10.

Other cross sectional studies show a direct correlation of aldosterone levels and impaired glucose metabolism in patients with and without the MetSyn 10;11. Taken together, aldosterone influences essential parameters of the MetSyn. Coincidentally parameters of the MetSyn are stimulus for an increased aldosterone synthesis, i.e. visceral adipocytes 12.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Patients with or without antihypertensive therapy and mean blood pressure > 160/100 mmHg
  • Patients with secondary hypertension
  • Patients with one antihypertensive agent maximally dosed or two (or less) agents with half (or less) of maximum approved dose
  • Patients with diabetes mellitus type 1 or type 2
  • Smokers and ex-smokers < 1 year
  • Female patients (to prevent effects of changes in endothelial function attributable to the menstrual cycle)
  • Patients with sick sinus syndrome
  • Patients with higher degree of sinoatrial or atrioventricular block (II-III)
  • Patients with bradycardia (< 50 beats/min)
  • Patients with malignant arrhythmias
  • Patients with known cardiovascular, disease
  • Patients with known cerebrovacular disease
  • Patients with peripheral occlusive artery disease
  • Patients with history of epilepsy
  • Patients with severe hepatic disease (serum GOT, GPT, gamma-GT, AP, bilirubin > 300 of uppper normal range)
  • Patients with renal disease defined by eGFR < 60 ml/min/1,73m2
  • Patients with history of malignant disease within the last 2 years
  • Patients with history of depression
  • Patients with drug or alcohol abuse
  • Use of any investigational drug within 28 days before study entry
  • Known allergy or a known intolerance to the study drug
  • Likelihood of requiring treatment during the study period with drugs not permitted by the clinical study protocol, especially likelihood of the need for additional antihypertensive medication
  • Serious disorders which may limit the ability to evaluate the efficacy or safety of the test drug(s), including cerebrovascular, cardiovascular, renal, respiratory, hepatic, gastrointestinal, endocrine or metabolic, haematological or oncological, neurological and psychiatric diseases
  • Subject is the investigator or any subinvestigator, research assistant, pharmacist, study coordinator, other staff or relative thereof directly involved in the conduct of the protocol
  • Mental conditions rendering the subject unable to understand the nature, scope and possible consequences of the study
  • Subject unlikely to comply with protocol, e.g. uncooperative attitude, inability to return for follow-up visits and unlikelihood of completing the study

研究组 & 干预措施

Eplerenone

Experimental

干预措施: Eplerenone (Drug)

结局指标

主要结局

Change of basal nitric oxide activity as assessed by change of retinal capillary flow (measured by Scanning Laser Doppler Flowmetry)

时间窗: Ten weeks

次要结局

  • Changes of distensibility of the carotid artery.(Ten weeks)
  • Change of flow mediated dilation of the brachial artery.(Ten weeks)

研究者

发起方
University of Erlangen-Nürnberg Medical School
申办方类型
Other
责任方
Principal Investigator
主要研究者

Roland E. Schmieder

Prof. Dr. med.

University of Erlangen-Nürnberg Medical School

研究点 (2)

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