Kario Kazuomi, Ito Sadayoshi, Itoh Hiroshi, Rakugi Hiromi, Okuda Yasuyuki, Yamakawa Satoru
Division of Cardiovascular Medicine, Department of Medicine, Jichi Medical University School of Medicine, Shimotsuke, Japan.
Division of Nephrology, Endocrinology and Vascular Medicine, Department of Medicine, Tohoku University School of Medicine, Sendai, Japan.
Am J Hypertens. 2025 Jul 15;38(8):605-611. doi: 10.1093/ajh/hpaf048.
Nocturnal blood pressure (BP) is superior to daytime BP in predicting cardiovascular mortality. It is of clinical relevance to evaluate the effect of esaxerenone combination therapy on nighttime BP in patients with uncontrolled hypertension.
A post hoc analysis of a multicenter, open-label, phase 3 study evaluated the nighttime BP-lowering effects of esaxerenone as monotherapy or in combination with a calcium channel blocker (CCB) or renin-angiotensin system inhibitor (RASi) in Japanese patients with uncontrolled hypertension. In addition, the effect on N-terminal pro B-type natriuretic peptide (NT-proBNP), a known biomarker of cardiovascular disease prognosis, was evaluated.
In total, 270 patients were included in this analysis (172, 49, and 49 patients in the monotherapy, CCB, and RASi groups, respectively). The 24-hour ambulatory systolic BP reduction from baseline was - 10.0, - 6.0, and - 17.0 mm Hg in the monotherapy, CCB, and RASi groups, respectively. Nighttime systolic BP decreased significantly from baseline to week 28 in all groups (P < 0.001 each); the RASi group showed the greatest change (- 20.6 mm Hg). NT-proBNP decreased significantly in all three treatment groups.
Esaxerenone when used in combination with a CCB or RASi, but especially when used in combination with a RASi, may be a useful treatment option for patients with uncontrolled hypertension to control nocturnal BP.
夜间血压在预测心血管死亡率方面优于日间血压。评估依沙库利酮联合治疗对未控制高血压患者夜间血压的影响具有临床意义。
一项多中心、开放标签、3期研究的事后分析评估了依沙库利酮单药治疗或与钙通道阻滞剂(CCB)或肾素-血管紧张素系统抑制剂(RASi)联合使用对日本未控制高血压患者夜间血压的降低作用。此外,还评估了对N端前B型利钠肽(NT-proBNP)的影响,NT-proBNP是心血管疾病预后的已知生物标志物。
本分析共纳入270例患者(单药治疗组、CCB组和RASi组分别为172例、49例和49例)。单药治疗组、CCB组和RASi组从基线开始的24小时动态收缩压降低分别为-10.0、-6.0和-17.0 mmHg。所有组夜间收缩压从基线到第28周均显著下降(每组P<0.001);RASi组变化最大(-20.6 mmHg)。所有三个治疗组的NT-proBNP均显著下降。
依沙库利酮与CCB或RASi联合使用时,尤其是与RASi联合使用时,可能是未控制高血压患者控制夜间血压的一种有效治疗选择。