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Mavacamten-Associated Temporal Changes in Left Atrial Function in Obstructive HCM: Insights From the VALOR-HCM Trial
Milind Y Desai1, Yuichiro Okushi2, Kathy Wolski3
1Hypertrophic Cardiomyopathy Center, Heart, Vascular and Thoracic Institute, Cleveland Clinic, Cleveland, Ohio, USA; Department of Cardiovascular Medicine, Heart, Vascular and Thoracic Institute, Cleveland Clinic, Cleveland, Ohio, USA; Cleveland Clinic Coordinating Center for Clinical Research, Heart, Vascular and Thoracic Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Insights
Mavacamten improved left atrial (LA) function and reduced LA volume index in patients with obstructive hypertrophic cardiomyopathy (HCM). These benefits were observed in the VALOR-HCM trial, except in patients with atrial fibrillation.
Area of Science:
- Cardiology
- Pharmacology
- Cardiac Imaging
Background:
- Obstructive hypertrophic cardiomyopathy (HCM) significantly impacts patient quality of life.
- Mavacamten has shown efficacy in reducing left ventricular outflow tract gradients and improving cardiac remodeling in HCM.
- The effect of mavacamten on left atrial (LA) function in HCM patients remained unclear.
Purpose of the Study:
- To evaluate the serial changes in left atrial (LA) strain parameters in patients with obstructive HCM participating in the VALOR-HCM trial.
- To assess the impact of mavacamten on LA function over 56 weeks.
Main Methods:
- The VALOR-HCM trial enrolled 112 symptomatic obstructive HCM patients.
- Patients received mavacamten or placebo, with placebo patients transitioning to mavacamten.
- Echocardiographic LA strain (reservoir, conduit, contraction) was measured using vendor-neutral software over 56 weeks.
Main Results:
- Mavacamten significantly improved LA volume index (LAVI) and all LA strain measures (conduit, contraction, reservoir) from baseline to week 56.
- Baseline LA measurements were worse than normal values.
- No significant improvement in LA strain was observed in patients with a history of atrial fibrillation.
Conclusions:
- Mavacamten treatment led to significant improvements in LAVI and LA strain, indicating favorable LA remodeling and function in obstructive HCM.
- The positive effects on LA function were not observed in the atrial fibrillation subgroup.
- Further research is needed to determine if mavacamten's LA remodeling benefits impact atrial tachyarrhythmias in HCM.
Background:
In severely symptomatic patients with obstructive hypertrophic cardiomyopathy (HCM), the VALOR-HCM (A Study to Evaluate Mavacamten in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Who Are Eligible for Septal Reduction Therapy) trial showed that mavacamten reduced the eligibility for septal reduction therapy with sustained improvement in left ventricular outflow tract gradients. Mavacamten also resulted in favorable cardiac remodeling, including improvement in biomarkers (eg, N-terminal pro-B-type natriuretic peptide and troponin T). However, the impact of mavacamten on left atrial (LA) function is unknown.
Objectives:
The aim of this study was to assess serial changes in LA strain measures in patients enrolled in the VALOR-HCM trial.
Methods:
VALOR-HCM included 112 symptomatic patients with obstructive HCM (mean age 60 years; 51% male). Patients assigned to receive mavacamten at baseline (n = 56) continued therapy for 56 weeks and those assigned to placebo transitioned to mavacamten (n = 52) from week 16 to week 56. Echocardiographic LA strain (reservoir, conduit, and contraction) was measured by using a vendor-neutral postprocessing software.
Results:
At baseline, the mean LA volume index (LAVI) and LA strain values (conduit, contraction, and reservoir) were 41.3 ± 16.5 mL/m2, -11.8% ± 6.5%, -8.7% ± 5.0%, and 20.5% ± 8.7%, respectively (all worse than reported normal). LAVI significantly improved by -5.6 ± 9.7 mL/m2 from baseline to week 56 (P < 0.001). There was a significant (P < 0.05) improvement in absolute LA strain values from baseline to week 56 (conduit [-1.7% ± 6%], contraction [-1.2% ± 4.5%], and reservoir [2.8% ± 7.7%]). Patients originally receiving placebo had no differences in LA measurements up to week 16. There was no significant improvement in LA strain values (conduit [-0.9% ± 3.8%], contraction [-0.4% ± 3.4%], and reservoir [1.4% ± 6.1%]; all; P = not significant) from baseline to week 56 in patients with history of atrial fibrillation.
Conclusions:
In VALOR-HCM, mavacamten resulted in an improvement in LAVI and LA strain at week 56, suggesting sustained favorable LA remodeling and improved function, except in the atrial fibrillation subgroup. Whether the advantageous LA remodeling associated with long-term treatment with mavacamten results in a favorable impact on the observed high burden of atrial tachyarrhythmias in HCM remains to be proven. (A Study to Evaluate Mavacamten in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Who Are Eligible for Septal Reduction Therapy [VALOR-HCM]; NCT04349072).
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