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Published on: November 29, 2024
Is Entresto good for the brain?
1Nirav Patel, Jason Gluck, Department of Cardiology, University of Connecticut, Harford Hospital, Hartford, CT 06102, United States.
Insights
Sacubitril-valsartan (SV) improves heart failure (HF) outcomes by targeting both the renin-angiotensin-aldosterone (RAAS) and neprilysin pathways (NP). Long-term monitoring is crucial to assess potential Alzheimer
Area of Science:
- Cardiology
- Pharmacology
- Neurology
Background:
- Current heart failure (HF) pharmacotherapy targets the renin-angiotensin-aldosterone (RAAS) and neprilysin pathways (NP).
- While effective in reducing morbidity and mortality, these therapies have notable adverse effects.
- Sacubitril-valsartan (SV), also known as Entresto, represents a novel approach by simultaneously inhibiting both RAAS and NP.
Purpose of the Study:
- To review the literature on the efficacy and safety of sacubitril-valsartan (SV) in heart failure management.
- To highlight the dual-action mechanism of SV as an angiotensin receptor blocker and neprilysin inhibitor (NPi).
- To investigate concerns regarding potential adverse effects, specifically the risk of Alzheimer's disease (AD).
Main Methods:
- Literature review of studies on sacubitril-valsartan (SV) in heart failure.
- Analysis of the pharmacological action of SV on RAAS and NP pathways.
- Examination of reported side effects, including cognitive changes and Alzheimer's disease (AD) risk.
Main Results:
- SV has demonstrated improved heart failure prognosis, marking an evolution in HF management.
- Initial follow-up data for SV treatment shows promising results.
- Concerns exist regarding a potential increased risk of Alzheimer's disease (AD) due to neprilysin inhibition's effect on beta-amyloid peptide clearance.
Conclusions:
- Sacubitril-valsartan (SV) offers a significant advancement in heart failure treatment through dual pathway inhibition.
- The potential link between neprilysin inhibition and Alzheimer's disease (AD) necessitates careful consideration.
- Extended patient follow-up is essential to monitor for any adverse cognitive changes in individuals treated with SV.
Abstract:
The main stay pharmacotherapy for heart failure (HF) is targeted towards rennin-angiotensin-aldosterone (RAAS) and neprilysin pathways (NP). Both therapeutic strategies decreases morbidity and mortality but also carry considerable adverse effects. This review of the literature highlights the new generation of HF drug, sacubitril-valsartan (SV), trade name Entresto (researched as LCZ696, Novartis) which simultaneously blocks RAAS and NP. This dual action of angiotensin receptors blocker and neprilysin inhibitor (NPi) has improved HF prognosis and it is an evolution in the management of HF. Although the initial follow-up of patients treated with SV has yielded promising results, there are concerns regarding potential side effects especially an increase in the risk of Alzheimer's disease (AD) and young onset of AD. NPi interferes with the breakdown and clearing of beta-amyloid peptides, the plaques seen in AD, raising concern for AD in SV patients. On the other hand, hypertension and cardiovascular diseases are established risk factors for AD which can be decreased by SV therapy. It is therefore essential that SV treated patients are followed up over an extended period of time to detect any adverse cognitive changes.
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