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Improved Renal Denervation Mitigated Hypertension Induced by Angiotensin II Infusion
Published on: May 26, 2022
Prognostic and Safety Implications of Renin-Angiotensin-Aldosterone System Inhibitors in Hypertrophic Cardiomyopathy:
Chan Soon Park1, Tae-Min Rhee1, Hyun Jung Lee1,2
1Cardiovascular Center, Seoul National University Hospital, Seoul, Korea.
Insights
Renin-angiotensin-aldosterone system inhibitors (RASi) did not worsen outcomes in hypertrophic cardiomyopathy (HCM) patients. This study suggests RASi can be safely used in HCM patients when clinically indicated.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Renin-angiotensin-aldosterone system inhibitors (RASi) use in hypertrophic cardiomyopathy (HCM) is debated due to concerns about worsening left ventricular outflow tract (LVOT) obstruction.
- The prognostic and safety implications of RASi in HCM remain incompletely understood.
Purpose of the Study:
- To investigate the safety and prognostic implications of RASi in a large cohort of patients diagnosed with HCM.
- To evaluate the association between RASi use and clinical outcomes, including all-cause mortality and heart failure hospitalizations.
Main Methods:
- A total of 2,104 patients with HCM were enrolled from two tertiary university hospitals and followed for five years.
- RASi use was defined as administration after HCM diagnosis. Primary outcomes were all-cause mortality and hospitalization for heart failure (HHF).
- Multivariable and subgroup analyses were performed to assess the impact of RASi on outcomes, considering factors like LVOT obstruction and LV ejection fraction.
Main Results:
- RASi were prescribed to 36.2% of patients. Over a median follow-up of 48.1 months, 5.3% died and 4.5% were hospitalized for heart failure.
- Despite baseline differences, RASi use was not associated with significantly different rates of all-cause mortality or HHF compared to non-RASi users.
- Subgroup analyses showed no significant interaction between RASi use and LVOT obstruction, LV ejection fraction, or LV wall thickness.
Conclusions:
- RASi use was not associated with adverse clinical outcomes in patients with hypertrophic cardiomyopathy.
- RASi may be safely administered to HCM patients when clinically indicated, challenging previous concerns about LVOT obstruction aggravation.
Background And Objectives:
The prognostic or safety implication of renin-angiotensin-aldosterone system inhibitors (RASi) in hypertrophic cardiomyopathy (HCM) are not well established, mainly due to concerns regarding left ventricular outflow tract (LVOT) obstruction aggravation. We investigated the implications of RASi in a sizable number of HCM patients.
Methods:
We enrolled 2,104 consecutive patients diagnosed with HCM in 2 tertiary university hospitals and followed up for five years. RASi use was defined as the administration of RASi after diagnostic confirmation of HCM. The primary and secondary outcomes were all-cause mortality and hospitalization for heart failure (HHF).
Results:
RASi were prescribed to 762 patients (36.2%). During a median follow-up of 48.1 months, 112 patients (5.3%) died, and 94 patients (4.5%) experienced HHF. Patients using RASi had less favorable baseline characteristics than those not using RASi, such as older age, more frequent history of comorbidities, and lower ejection fraction. Nonetheless, there was no difference in clinical outcomes between patients with and without RASi use (log-rank p=0.368 for all-cause mortality and log-rank p=0.443 for HHF). In multivariable analysis, patients taking RASi showed a comparable risk of all-cause mortality (hazard ratio [HR], 0.70, 95% confidence interval [CI], 0.43-1.14, p=0.150) and HHF (HR, 1.03, 95% CI, 0.63-1.70, p=0.900). In the subgroup analysis, there was no significant interaction of RASi use between subgroups stratified by LVOT obstruction, left ventricular (LV) ejection fraction, or maximal LV wall thickness.
Conclusions:
RASi use was not associated with worse clinical outcomes. It might be safely administered in patients with HCM if clinically indicated.
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