Department of Medicine II, Endocrinology and Hypertension, Tokyo Women's Medical University, Tokyo, Japan.
Department of Medical Education, Tokyo Women's Medical University, Tokyo, Japan.
Hypertens Res. 2018 Jun;41(6):435-443. doi: 10.1038/s41440-018-0037-1. Epub 2018 Apr 4.
The (pro)renin receptor is important in the regulation of the tissue renin-angiotensin-aldosterone system. The benefits and safety of single-aliskiren treatment without other renin-angiotensin-aldosterone system inhibitors remain unclear. The serum level of the soluble form of the (pro)renin receptor is thought to be a biomarker reflecting the activity of the tissue renin-angiotensin-aldosterone system. We investigated the effects of single renin-angiotensin-aldosterone system blockade with aliskiren on renal and vascular functions and determined if serum level of the soluble (pro)renin receptor was a predictor of aliskiren efficacy in hypertensive patients with chronic kidney disease. Thirty-nine essential hypertensive patients with chronic kidney disease in our outpatient clinic were randomly assigned to receive either aliskiren or amlodipine. The parameters associated with renal and vascular functions and indices of renin-angiotensin-aldosterone system components, including serum levels of the soluble form, were evaluated before and after 12-week and 24-week treatment. Blood pressure was not significantly different between the groups. No significant changes in serum levels were observed in the soluble (pro)renin receptor in either group. Urinary albumin, protein excretion, and cardio-ankle vascular index significantly decreased in the aliskiren group. In the aliskiren group, there was a significant negative correlation between the basal level of the soluble (pro)renin receptor and the change in plasma aldosterone concentration. Single renin-angiotensin-aldosterone system blockade with aliskiren showed renal and vascular protective effects independent of blood pressure reduction. Serum levels of the soluble (pro)renin receptor may indicate aldosterone production via the (pro)renin receptor in the adrenal gland.
(前)肾素受体在组织肾素-血管紧张素-醛固酮系统的调节中起着重要作用。单一使用阿利克仑治疗而不联合使用其他肾素-血管紧张素-醛固酮系统抑制剂的益处和安全性尚不清楚。可溶性(前)肾素受体的血清水平被认为是反映组织肾素-血管紧张素-醛固酮系统活性的生物标志物。我们研究了单一肾素-血管紧张素-醛固酮系统阻断剂阿利克仑对肾脏和血管功能的影响,并确定血清可溶性(前)肾素受体水平是否可预测高血压合并慢性肾脏病患者使用阿利克仑的疗效。我们在门诊随机分配 39 例原发性高血压合并慢性肾脏病患者接受阿利克仑或氨氯地平治疗。治疗前、治疗 12 周和 24 周后,评估与肾脏和血管功能相关的参数以及肾素-血管紧张素-醛固酮系统成分的指标,包括血清可溶性形式的水平。两组的血压无显著差异。两组的可溶性(前)肾素受体血清水平均无显著变化。阿利克仑组的尿白蛋白、蛋白排泄和心踝血管指数显著降低。在阿利克仑组,基础水平的可溶性(前)肾素受体与血浆醛固酮浓度变化之间存在显著的负相关。单独使用阿利克仑阻断肾素-血管紧张素-醛固酮系统具有独立于降压作用的肾脏和血管保护作用。血清可溶性(前)肾素受体水平可能表明醛固酮通过肾上腺中的(前)肾素受体产生。