John W Ostrominski, Brian L Claggett, Ian J Kulac, Akshay S Desai, Pardeep S Jhund, Alasdair Henderson, Carolyn S P Lam, Michele Senni, Sanjiv J Shah, Adriaan A Voors, Faiez Zannad, Bertram Pitt, Meike Brinker, Patrick Schloemer, Flaviana Amarante, Lucas Hofmeister, John J V McMurray, Scott D Solomon, Muthiah Vaduganathan
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引用次数: 0
Abstract
Aims: Apparent treatment-resistant hypertension (aTRH) is common and associated with adverse outcomes in individuals with heart failure (HF) with mildly reduced or preserved ejection fraction (HFmrEF/HFpEF). Whether finerenone improves blood pressure (BP) and clinical outcomes in individuals with HFmrEF/HFpEF and aTRH is uncertain.
Methods: In this pre-specified analysis of the FINEARTS-HF trial, participants were categorized according to baseline BP, with aTRH defined as BP ≥140/90 mm Hg (≥130/80 mm Hg if diabetes) despite treatment with ≥3 BP-lowering medications, including a diuretic. Non-resistant hypertension was defined as BP above threshold but not meeting aTRH criteria. Controlled BP was defined as BP under the threshold. Incidence of clinical outcomes and safety events was assessed by baseline hypertension category.
Results: Among 6001 participants, 3471 (57.8%) had controlled blood pressure, 1754 (29.2%) had non-resistant hypertension, and 776 (12.9%) had aTRH at baseline. Between baseline and 36 months, finerenone similarly reduced systolic BP across baseline BP categories (Pinteraction = 0.59). Rates of cardiovascular death and total HF events (per 100 person-years) were 17.0 in those with controlled BP, 16.0 in those with non-resistant hypertension, and 13.8 in those with aTRH (Pcomparison = 0.12). Relative treatment benefits of finerenone vs placebo on the primary outcome (Pinteraction = 0.32) and HF-related health status (Pinteraction = 0.22) were consistent across hypertension categories. The safety profile of finerenone vs placebo did not appear to be modified by baseline hypertension category.
Conclusion: aTRH was identified in 1-in-8 individuals with HFmrEF/HFpEF in FINEARTS-HF. Finerenone consistently improved clinical outcomes, health status, and blood pressure, including among those with aTRH.
目的:明显的治疗抵抗性高血压(aTRH)在射血分数轻度降低或保持的心力衰竭(HF)患者中很常见,并与不良结局相关。芬尼酮是否能改善HFmrEF/HFpEF和aTRH患者的血压(BP)和临床结果尚不确定。方法:在这项预先指定的FINEARTS-HF试验分析中,参与者根据基线血压进行分类,尽管接受了包括利尿剂在内的≥3种降压药物治疗,但aTRH定义为血压≥140/90 mm Hg(糖尿病患者≥130/80 mm Hg)。非顽固性高血压定义为血压高于阈值但不符合aTRH标准。控制血压定义为阈值以下的血压。临床结果和安全事件的发生率通过基线高血压分类进行评估。结果:在6001名参与者中,3471人(57.8%)血压得到控制,1754人(29.2%)患有非顽固性高血压,776人(12.9%)在基线时患有aTRH。在基线和36个月之间,芬烯酮在基线血压类别中相似地降低了收缩压(p相互作用= 0.59)。血压控制组心血管死亡和总HF事件发生率(每100人年)为17.0,非顽固性高血压组为16.0,aTRH组为13.8 (p比较= 0.12)。芬尼酮与安慰剂在主要结局(p相互作用= 0.32)和hf相关健康状况(p相互作用= 0.22)方面的相对治疗益处在高血压类别中是一致的。芬尼酮与安慰剂的安全性似乎没有因基线高血压类别而改变。结论:在FINEARTS-HF中,每8例HFmrEF/HFpEF患者中就有1例发现aTRH。芬尼酮持续改善临床结果、健康状况和血压,包括aTRH患者。
期刊介绍:
European Journal of Heart Failure is an international journal dedicated to advancing knowledge in the field of heart failure management. The journal publishes reviews and editorials aimed at improving understanding, prevention, investigation, and treatment of heart failure. It covers various disciplines such as molecular and cellular biology, pathology, physiology, electrophysiology, pharmacology, clinical sciences, social sciences, and population sciences. The journal welcomes submissions of manuscripts on basic, clinical, and population sciences, as well as original contributions on nursing, care of the elderly, primary care, health economics, and other related specialist fields. It is published monthly and has a readership that includes cardiologists, emergency room physicians, intensivists, internists, general physicians, cardiac nurses, diabetologists, epidemiologists, basic scientists focusing on cardiovascular research, and those working in rehabilitation. The journal is abstracted and indexed in various databases such as Academic Search, Embase, MEDLINE/PubMed, and Science Citation Index.