Renin-Angiotensin System Blockade in Aortic Stenosis: Implications Before and After Aortic Valve Replacement

Aortic stenosis (AS) is a common valvular heart disease in the aging population that is characterized by a variable period of asymptomatic phase before development of symptoms and severe AS. Mortality and morbidity is substantial even after aortic valve replacement, in part related to persistent lef...

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Published inJournal of the American Heart Association Vol. 9; no. 18; p. e016911
Main Authors Goel, Sachin S, Kleiman, Neal S, Zoghbi, William A, Reardon, Michael J, Kapadia, Samir R
Format Journal Article
LanguageEnglish
Published England John Wiley and Sons Inc 15.09.2020
Wiley
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Summary:Aortic stenosis (AS) is a common valvular heart disease in the aging population that is characterized by a variable period of asymptomatic phase before development of symptoms and severe AS. Mortality and morbidity is substantial even after aortic valve replacement, in part related to persistent left ventricular hypertrophy, diastolic dysfunction, and heart failure. Renin-angiotensin system (RAS) blockade therapy is associated with modulation of adverse left ventricular remodeling, reduction in myocardial hypertrophy, and fibrosis, resulting in clinical improvements in patients with congestive heart failure There are emerging data to suggest benefit of RAS blockade in patients with AS before and after AVR with regard to potentially slower progression of aortic valve calcification, left ventricular mass and survival benefit in favor of RAS blockade group before AVR, and also survival benefit in patients after AVR. We review the available data to understand the role of RAS blockade before AVR and in patients undergoing surgical AVR and transcatheter AVR. There are significant survival advantages of RAS inhibition in patients with AS undergoing surgical AVR or transcatheter AVR. On the basis of existing literature, adequately powered randomized trials are needed to evaluate the role of RAS inhibition in patients with AS.
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For Disclosures, see page 10.
ISSN:2047-9980
2047-9980
DOI:10.1161/JAHA.120.016911