Sustained Remission of New-onset Heart Failure in Genetic Cardiomyopathy Without Contemporary Four-pillar Therapy: Implications for ‘Personalized Guideline-directed Medical Therapy’

A 40-year-old woman with new-onset heart failure with reduced ejection fraction (HFrEF) attributed to a titin-truncating variant achieved remission while being treated with carvedilol, lisinopril (first 4 years), and losartan (for 1 year following lisinopril cessation). The patient never received an angiotensin receptor–neprilysin inhibitor, mineralocorticoid receptor antagonist, or sodium–glucose cotransporter 2 inhibitor. Her left ventricular ejection fraction rose from <25% to >50%, her N-terminal pro-B-type natriuretic peptide level dropped from 1,980 pg/ml to 79 pg/ml, and she regained New York Heart Association I status. Her remission persists more than a decade after condition onset. This case demonstrates that patients with genetic cardiomyopathy can achieve durable remission with a narrower set of medications than quadruple therapy.

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Publication Details

Journal
US Cardiology Review
Published
2026-11-06
DOI
https://doi.org/10.15420/usc.2026.26
Primary Topic
Heart Failure Treatment and Management
Type
article
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article

Sustained Remission of New-onset Heart Failure in Genetic Cardiomyopathy Without Contemporary Four-pillar Therapy: Implications for ‘Personalized Guideline-directed Medical Therapy’

Jennifer T. Thibodeau, Michael Pitonak, Mark H. Drazner, Jake Munch et al.
4 links
US Cardiology Review
Heart Failure Treatment and Management
article

Sustained Remission of New-onset Heart Failure in Genetic Cardiomyopathy Without Contemporary Four-pillar Therapy: Implications for ‘Personalized Guideline-directed Medical Therapy’

Jennifer T. Thibodeau, Michael Pitonak, Mark H. Drazner, Jake Munch, Chinanuekpere Emma Ezeala
article en

Abstract

A 40-year-old woman with new-onset heart failure with reduced ejection fraction (HFrEF) attributed to a titin-truncating variant achieved remission while being treated with carvedilol, lisinopril (first 4 years), and losartan (for 1 year following lisinopril cessation). The patient never received an angiotensin receptor–neprilysin inhibitor, mineralocorticoid receptor antagonist, or sodium–glucose cotransporter 2 inhibitor. Her left ventricular ejection fraction rose from <25% to >50%, her N-terminal pro-B-type natriuretic peptide level dropped from 1,980 pg/ml to 79 pg/ml, and she regained New York Heart Association I status. Her remission persists more than a decade after condition onset. This case demonstrates that patients with genetic cardiomyopathy can achieve durable remission with a narrower set of medications than quadruple therapy.

US Cardiology Review
The University of Texas Southwestern Medical Center (US)
Good health and well-being
Openalex Percentile: Top 13%
Heart Failure Treatment and Management
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