Division of Cardiovascular Medicine, Department of Medicine, Jichi Medical University School of Medicine, Shimotsuke, Tochigi, Japan.
Division of Nephrology, Endocrinology and Vascular Medicine, Department of Medicine, Tohoku University School of Medicine, Sendai, Japan.
Hypertens Res. 2022 Jan;45(1):97-105. doi: 10.1038/s41440-021-00756-5. Epub 2021 Oct 15.
There are limited data on the nighttime blood pressure (BP)-lowering effect of esaxerenone and its effect on N-terminal pro b-type natriuretic peptide (NT-proBNP), a predictor of cardiovascular risk, according to different dipping patterns of nocturnal BP. This was a post hoc analysis of a multicenter, open-label, long-term phase 3 study of esaxerenone, a new highly selective mineralocorticoid receptor blocker, in patients with essential hypertension. Patients were classified by dipping pattern (extreme dippers, dippers, non-dippers, risers). Mean changes in BP, changes in dipping pattern, mean NT-proBNP levels, and percentage of patients with normal NT-proBNP levels (<55 pg/mL) at baseline and Weeks 12 and 28 were evaluated. Nighttime systolic BP decreased in all dipping pattern groups at Week 28, with the riser group showing the greatest change (-25.5 mmHg). A significant shift in dipping pattern and riser/non-dipper pattern changes to dipper/extreme dipper pattern were found from baseline to Week 28 (p < 0.0001). The prevalence of the riser pattern decreased from 14.4% to 9.8%, and that of the non-dipper pattern from 44.7% to 39.2%. The decrease in NT-proBNP from baseline to Week 28 was statistically significant in risers, non-dippers, dippers, and extreme dippers (p < 0.001, respectively). At baseline, the proportion of patients with NT-proBNP <55 pg/mL was lowest in risers versus the other dipping pattern types, but after reductions in NT-proBNP in all groups to Week 28, these differences disappeared. Long-term administration of esaxerenone may be a useful treatment option for nocturnal hypertension, especially in patients with a riser pattern.
根据不同的夜间血压(BP)下降模式和夜间 BP 下降模式的预测心血管风险的 N 末端 pro B 型利钠肽(NT-proBNP),有关依普利酮的夜间 BP 降压作用及其对 NT-proBNP 的影响的数据有限。这是一项多中心、开放标签、长期 3 期研究的事后分析,研究对象为原发性高血压患者,接受新型高度选择性盐皮质激素受体阻滞剂依普利酮治疗。根据夜间 BP 下降模式(极夜型、夜间下降型、非夜间下降型、夜间升高型)对患者进行分类。评估降压治疗 28 周时 BP 的平均变化、夜间 BP 下降模式的变化、平均 NT-proBNP 水平、以及治疗基线和 12 周及 28 周时 NT-proBNP 水平正常(<55pg/mL)的患者比例。夜间收缩压在所有夜间 BP 下降模式组中均下降,夜间升高组的变化最大(-25.5mmHg)。从基线到 28 周时,夜间 BP 下降模式发生了显著变化,夜间升高/非夜间下降型模式转变为夜间下降/极夜型模式(p<0.0001)。夜间升高型模式的发生率从 14.4%下降至 9.8%,非夜间下降型模式的发生率从 44.7%下降至 39.2%。夜间升高组、非夜间下降组、夜间下降组和极夜型组从基线至 28 周时 NT-proBNP 下降有统计学意义(p<0.001)。基线时,夜间升高组患者的 NT-proBNP<55pg/mL 比例最低,而与其他夜间 BP 下降模式类型相比,但在所有组 NT-proBNP 降低至 28 周时,这些差异消失。长期服用依普利酮可能是治疗夜间高血压的一种有效治疗选择,尤其是对夜间升高型高血压患者。