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Published on: March 29, 2024
Sacubitril/Valsartan in Asian Patients with Heart Failure with Reduced Ejection Fraction
Pooja Dewan1, Kieran F Docherty1, John J V McMurray2
1British Heart Foundation Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
Insights
Sacubitril/valsartan, an Angiotensin Receptor-neprilysin inhibitor (ARNI), significantly reduced heart failure (HF) morbidity and mortality compared to an ACE inhibitor. This ARNI therapy is now approved for patients with heart failure with reduced ejection fraction (HFrEF).
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Heart failure with reduced ejection fraction (HFrEF) poses a significant global health burden, particularly in Asia.
- Current treatments, including Angiotensin converting enzyme inhibitors (ACEI), have limitations in managing HFrEF.
- The PARADIGM-HF trial investigated novel therapeutic approaches for HFrEF.
Purpose of the Study:
- To review the development and efficacy of sacubitril/valsartan, a novel Angiotensin Receptor-neprilysin inhibitor (ARNI).
- To evaluate the safety and effectiveness of sacubitril/valsartan in Asian patients with HFrEF.
- To compare ARNI therapy with standard ACEI treatment for HFrEF.
Main Methods:
- The review discusses data from the PARADIGM-HF trial, a prospective comparison of ARNI versus ACEI.
- Focuses on outcomes including cardiovascular death, HF hospitalization, and all-cause mortality.
- Examines evidence specific to the Asian population with HFrEF.
Main Results:
- Sacubitril/valsartan demonstrated superiority over enalapril (an ACEI) in reducing the primary composite outcome of cardiovascular death or HF hospitalization by 20%.
- ARNI therapy resulted in a 16% reduction in all-cause mortality compared to ACEI.
- The PARADIGM-HF trial led to regulatory approval of sacubitril/valsartan for HFrEF treatment.
Conclusions:
- Sacubitril/valsartan represents a significant advancement in HFrEF management, offering improved outcomes over traditional ACEI therapy.
- The efficacy and safety profile of sacubitril/valsartan in Asian populations with HFrEF warrant further consideration.
- This ARNI therapy is a crucial new option for patients with HFrEF globally and in Asia.
Abstract:
The Prospective comparison of Angiotensin Receptor-neprilysin inhibitor (ARNI) with Angiotensin converting enzyme inhibitor (ACEI) to Determine Impact on Global Mortality and morbidity in Heart Failure (HF) trial (PARADIGM-HF) showed that adding a neprilysin inhibitor (sacubitril) to a renin-angiotensin system blocker (and other standard therapy) reduced morbidity and mortality in ambulatory patients with chronic HF with reduced ejection fraction (HFrEF). In PARADIGM-HF, valsartan combined with sacubitril (a so-called ARNI) was superior to the current gold standard of an ACEI, specifically enalapril, reducing the risk of the primary composite outcome of cardiovascular (CV) death or first HF hospitalization by 20% and all-cause death by 16%. Following the results of PARADIGM-HF, sacubitril/valsartan was approved by American and European regulatory authorities for the treatment of HFrEF. The burden of HF in Asia is substantial, both due to the huge population of the region and as a result of increasing CV risk factors and disease. Both the prevalence and mortality associated with HF are high in Asia. In the following review, we discuss the development of sacubitril/valsartan, the prototype ARNI, and the available evidence for its efficacy and safety in Asian patients with HFrEF.
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