# One- and two-year structural changes of mavacamten therapy in hypertrophic obstructive cardiomyopathy: a case report with serial comprehensive CMR demonstrating continuous reverse remodelling

**Authors:** Katharina Seuthe, Roman Pfister, Carl-Hubertus Schönherr, Kenan Kaya, Lenhard Pennig

PMC · DOI: 10.1093/ehjcr/ytag165 · European Heart Journal. Case Reports · 2026-03-09

## TL;DR

This case report shows that mavacamten treatment for hypertrophic obstructive cardiomyopathy leads to long-term heart remodeling over two years.

## Contribution

The study provides the first detailed two-year CMR analysis of cardiac remodeling with mavacamten in HOCM.

## Key findings

- Mavacamten caused progressive reverse remodeling, including reduced LV ejection fraction and LV mass index over two years.
- Native T1 relaxation times decreased, while extracellular volume fraction initially increased but normalized by two years.
- Late gadolinium enhancement mass remained unchanged despite structural changes.

## Abstract

Hypertrophic obstructive cardiomyopathy (HOCM) is characterized by dynamic left ventricular outflow tract (LVOT) obstruction and impaired quality of life. Mavacamten, a first-in-class myosin inhibitor, offers a novel therapeutic approach for HOCM, which improves clinical symptoms and exercise capacity while leading to reduction of LVOT gradient and favourable cardiac remodelling in echocardiography and cardiovascular magnetic resonance (CMR). However, data on CMR-derived treatment effects remain limited to short follow-up studies.

A 39-year-old male with symptomatic HOCM refractory to bisoprolol and disopyramide was initiated on mavacamten therapy. Serial CMR after one and two years demonstrated progressive reverse remodelling over the follow-up period, including ongoing reduction of LV ejection fraction and LV mass index. While late gadolinium enhancement mass remained unchanged, there were divergent changes to measures of interstitial fibrosis: While native T1 relaxation times steadily decreased, extracellular volume (ECV) fraction initially increased but normalized at two-year follow-up.

This case indicates that mavacamten leads to longer-term cardiac remodelling up to two years after initiation of treatment, beyond early haemodynamic improvement and reduction of LVOT obstruction. These observations nurture additional studies to investigate longer-term effects on myocardial structure, function, and interstitial fibrosis.

## Linked entities

- **Chemicals:** mavacamten (PubChem CID 117761397)

## Full-text entities

- **Genes:** MYH14 (myosin heavy chain 14) [NCBI Gene 79784] {aka DFNA4, DFNA4A, FP17425, MHC16, MYH17, NMHC II-C}
- **Diseases:** heart failure (MESH:D006333), ) obstruction (MESH:D000402), HCM (MESH:D000092183), myocardial hypertrophy (MESH:D006984), mitral regurgitation (MESH:D008944), cardiac remodelling (MESH:D020257), ventricular arrhythmias (MESH:D001145), systolic murmur (MESH:D054160), ventricular tachycardia (MESH:D017180), genetic disorder (MESH:D030342), atrial fibrillation (MESH:D001281), SCD (MESH:D016757), SAM (MESH:D009041), LV hypertrophy (MESH:D017379), fibrosis (MESH:D005355), HOCM (MESH:D002312), CMR (MESH:D002318), LVOT obstruction (MESH:D000092242), cardiomyopathies (MESH:D009202), myocardial remodelling (MESH:D064752), dizziness (MESH:D004244), syncope (MESH:D013575), LGE (MESH:C564835)
- **Chemicals:** Mavacamten (MESH:C000605992), gadolinium (MESH:D005682), disopyramide (MESH:D004206), BioRender (-), bisoprolol (MESH:D017298)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13008283/full.md

## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC13008283/full.md

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Source: https://tomesphere.com/paper/PMC13008283