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Improved Renal Denervation Mitigated Hypertension Induced by Angiotensin II Infusion
Published on: May 26, 2022
Management of hypertension associated with cardiovascular failure
Shunsuke Kiuchi1, Takanori Ikeda1
1Department of Cardiovascular Medicine, Toho University Graduate School of Medicine, Tokyo, Japan.
Insights
Strict blood pressure control prevents heart failure (HF) progression. However, optimal targets differ for HF with reduced or preserved ejection fraction (HFrEF/HFpEF), necessitating tailored antihypertensive strategies.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Hypertension (HT) management is crucial for preventing heart failure (HF) incidence, particularly in Japan.
- The SPRINT trial demonstrated that a blood pressure (BP) target of ~120 mmHg inhibits HF progression in early stages (A and B).
- HF stages C and D require distinct BP targets based on ejection fraction (EF), differentiating between HF with reduced EF (HFrEF) and HF with preserved EF (HFpEF).
Purpose of the Study:
- To analyze the relationship between BP control and HF prognosis, considering the J-curve phenomenon.
- To investigate the role of vascular insufficiency in HF pathophysiology and its impact on antihypertensive treatment.
- To guide the selection of antihypertensive medications with cardioprotective effects, considering compelling indications.
Main Methods:
- Review of existing clinical trial data, including the SPRINT trial.
- Analysis of the J-curve phenomenon in relation to BP control in HFrEF and HFpEF.
- Evaluation of antihypertensive medication strategies, including uptitration and combination therapy.
Main Results:
- A BP target of approximately 120 mmHg is effective for early HF stages.
- HFpEF patients may require lower BP targets than HFrEF patients due to associated vascular failure.
- Optimal antihypertensive strategies must consider vascular status and individual patient factors.
Conclusions:
- Antihypertensive treatment must be individualized, considering HF type (HFrEF vs. HFpEF) and vascular health.
- Cardioprotective medication selection and management (e.g., ACE inhibitors/ARBs, beta-blockers) require careful consideration of onset, half-life, and patient-specific factors.
- Further research is needed on the optimal use of cardioprotective medications in specific populations, including elderly patients with HFrEF.
Abstract:
Hypertension (HT) treatment should focus on the prevention of new-onset heart failure (HF) or its exacerbation due to the increasing trend of HF incidence in Japan. According to the SPRINT trial, strict control of blood pressure (BP) of approximately 120 mmHg suppresses the progression of HF stages A and B to a more severe stage. However, in stages C and D, the target value for BP reduction differs depending on whether HF is HF reduced ejection fraction (EF) (HFrEF) or HF preserved EF (HFpEF). Additionally, the relationship between BP control and the prognosis of HF mostly showed the J-curve phenomenon in both HFrEF and HFpEF; however, patients with HFpEF need a lower target BP value than those with HFrEF. One reason is that vascular failure is associated with the pathophysiology of HF. Therefore, it is important to utilize an antihypertensive treatment strategy that considers vascular insufficiency. In addition, the presence or absence of compelling indications is important for the selection of antihypertensive (with cardioprotective effects for HF) medications. The uptitration of cardioprotective medications such as angiotensin-converting enzyme inhibitors/angiotensin II type 1a receptor blockers and beta-blockers is recommended in patients with HFrEF; however, it is often not practically possible to increase the dosage. In these cases, the use of medications in combination with other medication classes is also useful. Moreover, it is also useful to properly use medications of the same class considering their onset of action and half-life in the blood. It is still unclear how cardioprotective medications are used in patients with HFrEF, especially on certain age groups. The optimal initiation and continuation of cardioprotective medications should be carefully determined.
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