Freel E M, Tsorlalis I K, Lewsey J D, Latini R, Maggioni A P, Solomon S, Pitt B, Connell J M C, McMurray J J V
BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow G12 8TA, UK.
Heart. 2009 Dec;95(23):1920-4. doi: 10.1136/hrt.2009.173344. Epub 2009 Aug 26.
Aldosterone has a key role in the pathophysiology of heart failure. In around 50% of such patients, aldosterone "escapes" from inhibition by drugs that interrupt the renin-angiotensin axis; such patients have a worse clinical outcome. Insulin resistance is a risk factor in heart failure and cardiovascular disease. The relation between aldosterone status and insulin sensitivity was investigated in a cohort of heart failure patients.
302 patients with New York Heart Association (NYHA) class II-IV heart failure on conventional therapy were randomised in the ALiskiren Observation of heart Failure Treatment study (ALOFT), designed to test the safety of a directly acting renin inhibitor. Plasma aldosterone and 24-hour urinary aldosterone excretion, as well as fasting insulin and homeostasis model assessment of insulin resistance (HOMA-IR) were measured. Subjects with aldosterone escape and high urinary aldosterone were identified according to previously accepted definitions.
20% of subjects demonstrated aldosterone escape and 34% had high urinary aldosterone levels. At baseline, there was a positive correlation between fasting insulin and plasma (r = 0.22 p<0.01) and urinary aldosterone(r = 0.19 p<0.03). Aldosterone escape and high urinary aldosterone subjects both demonstrated higher levels of fasting insulin (p<0.008, p<0.03), HOMA-IR (p<0.06, p<0.03) and insulin-glucose ratios (p<0.006, p<0.06) when compared to low aldosterone counterparts. All associations remained significant when adjusted for potential confounders.
This study demonstrates a novel direct relation between aldosterone status and insulin resistance in heart failure. This observation merits further study and may identify an additional mechanism that contributes to the adverse clinical outcome associated with aldosterone escape.
醛固酮在心力衰竭的病理生理过程中起关键作用。在大约50%的此类患者中,醛固酮会从抑制肾素 - 血管紧张素轴的药物抑制作用中“逃逸”;这类患者临床结局更差。胰岛素抵抗是心力衰竭和心血管疾病的一个危险因素。在一组心力衰竭患者中研究了醛固酮状态与胰岛素敏感性之间的关系。
在阿利吉仑心力衰竭治疗观察研究(ALOFT)中,将302例接受常规治疗的纽约心脏协会(NYHA)II - IV级心力衰竭患者随机分组,该研究旨在测试一种直接作用的肾素抑制剂的安全性。测量了血浆醛固酮、24小时尿醛固酮排泄量,以及空腹胰岛素和胰岛素抵抗的稳态模型评估(HOMA - IR)。根据先前公认的定义确定醛固酮逃逸和尿醛固酮高的受试者。
20%的受试者表现出醛固酮逃逸,34%的受试者尿醛固酮水平高。在基线时,空腹胰岛素与血浆醛固酮(r = 0.22,p<0.01)和尿醛固酮(r = 0.19,p<0.03)之间存在正相关。与醛固酮水平低的对应者相比,醛固酮逃逸和尿醛固酮高的受试者空腹胰岛素水平(p<0.008,p<0.03)、HOMA - IR(p<0.06,p<0.03)和胰岛素 - 葡萄糖比值(p<0.006,p<0.06)均更高。在对潜在混杂因素进行调整后,所有关联仍具有显著性。
本研究证明了心力衰竭中醛固酮状态与胰岛素抵抗之间存在一种新的直接关系。这一观察结果值得进一步研究,可能会发现导致与醛固酮逃逸相关的不良临床结局的另一种机制。