Key result
Dual therapy with carvedilol and an ACEi/ARB sustains >10-year HFrEF remission in a case report.
Case Report (n=1)
This case report suggests that selected patients with HFrEF secondary to a titin-truncating variant may achieve durable, decade-long remission using beta-blocker and renin-angiotensin system inhibition alone without contemporary four-pillar therapy.
Answers are grounded in this paper and cite their sources.
Challenges mandatory quadruple therapy in titin-variant HFrEF; extends support for genotype-guided personalization in genetic cardiomyopathy.
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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Ezeala et al. (2026) conducted a case report in New-onset heart failure with reduced ejection fraction (HFrEF) attributed to a titin-truncating variant (n=1). Carvedilol, lisinopril (first 4 years), and losartan (1 year) was evaluated on Heart failure remission (LVEF recovery, NT-proBNP reduction, and NYHA functional status). Treatment with carvedilol and lisinopril/losartan without quadruple therapy achieved >10-year HFrEF remission, raising LVEF from <25% to >50% and lowering NT-proBNP from 1,980 to 79 pg/ml.
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