Maeda Daichi, Dotare Taishi, Matsue Yuya, Teramoto Kanako, Sunayama Tsutomu, Tromp Jasper, Minamino Tohru
Department of Cardiovascular Biology and Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
National Heart Centre, Singapore, Singapore.
Hypertens Res. 2023 Apr;46(4):817-833. doi: 10.1038/s41440-022-01158-x. Epub 2023 Jan 5.
Hypertension is a leading cause of heart failure and other cardiovascular diseases. Its role in the pathogenesis of heart failure with reduced ejection fraction (HFrEF) differs from that in heart failure with preserved ejection fraction (HFpEF). Moreover, rigorous blood pressure control may reduce the incidence of heart failure. However, once heart failure develops, prognosis is affected by blood pressure, which may differ between patients with and without heart failure. Therefore, the association between guideline-directed medical therapy (GDMT) for heart failure and its uptitration must be considered for blood pressure management and should not be overlooked. Heart failure medications affect the blood pressure and efficacy per baseline blood pressure value. This review discusses the potential mechanisms by which hypertension leads to HFrEF or HFpEF, the impact of hypertension on incident heart failure, and the recommended approaches for blood pressure management in patients with heart failure. Comparison between patients with and without heart failure regarding blood pressure The association between CV events and SBP is linear in patients without heart failure; however, it becomes J-shaped or inverse linear in those with heart failure. The management of BP, including optimal BP or pharmacotherapy, differs between the two populations. ACEi angiotensin-converting enzyme inhibitors, ARB angiotensin II receptor blockers; ARNi angiotensin receptor-neprilysin inhibitors, BB beta-blockers, BP blood pressure, CV cardiovascular, DASH Dietary Approaches to Stop Hypertension, GDMT guideline-directed medical therapy, HF heart failure, HFrEF heart failure with reduced ejection fraction, MRA mineralocorticoid receptor antagonists, SBP systolic blood pressure, SGLT2i sodium-glucose cotransporter 2 inhibitors.
高血压是心力衰竭和其他心血管疾病的主要病因。其在射血分数降低的心力衰竭(HFrEF)发病机制中的作用与射血分数保留的心力衰竭(HFpEF)不同。此外,严格控制血压可降低心力衰竭的发生率。然而,一旦发生心力衰竭,血压会影响预后,心力衰竭患者与非心力衰竭患者的情况可能有所不同。因此,在进行血压管理时必须考虑心力衰竭的指南导向药物治疗(GDMT)及其滴定增加情况,不容忽视。心力衰竭药物会根据基线血压值影响血压和疗效。本综述讨论了高血压导致HFrEF或HFpEF的潜在机制、高血压对新发心力衰竭的影响以及心力衰竭患者血压管理的推荐方法。心力衰竭患者与非心力衰竭患者血压的比较 在非心力衰竭患者中,心血管事件与收缩压(SBP)之间的关联呈线性;然而,在心力衰竭患者中则呈J形或反线性。这两类人群在血压管理方面存在差异,包括最佳血压或药物治疗。ACEi:血管紧张素转换酶抑制剂,ARB:血管紧张素II受体阻滞剂;ARNi:血管紧张素受体脑啡肽酶抑制剂,BB:β受体阻滞剂,BP:血压,CV:心血管,DASH:终止高血压膳食疗法,GDMT:指南导向药物治疗,HF:心力衰竭,HFrEF:射血分数降低的心力衰竭,MRA:盐皮质激素受体拮抗剂,SBP:收缩压,SGLT2i:钠-葡萄糖协同转运蛋白2抑制剂