Serial Changes in Ventricular Strain in Symptomatic Obstructive Hypertrophic Cardiomyopathy Treated With Mavacamten:
Milind Y Desai1,2,3, Yuichiro Okushi1,2, Andrew Gaballa1,2
1Hypertrophic Cardiomyopathy Center (M.Y.D., Y.O., A.G., Z.B.P.), Heart Vascular and Thoracic Institute, Cleveland Clinic, OH.
Insights
Mavacamten treatment improved left ventricular strain in obstructive hypertrophic cardiomyopathy patients. This cardiac myosin inhibitor showed no adverse effects on right ventricular strain.
Area of Science:
- Cardiology
- Cardiac Imaging
- Pharmacology
Background:
- Obstructive hypertrophic cardiomyopathy (oHCM) significantly impacts patients' quality of life.
- Mavacamten has shown promise in reducing symptoms and left ventricular (LV) outflow tract gradients in oHCM.
- Global longitudinal strain (GLS) is a sensitive indicator of myocardial systolic function.
Purpose of the Study:
- To assess the impact of mavacamten on serial changes in LV and right ventricular (RV) strain in patients with symptomatic oHCM.
- To evaluate LV-GLS and RV-GLS as markers of systolic function during mavacamten treatment.
Main Methods:
- The VALOR-HCM study enrolled 112 patients with symptomatic oHCM.
- Patients received mavacamten or placebo for 56 weeks, with placebo patients transitioning to mavacamten.
- LV-GLS and RV-GLS were assessed using vendor-neutral software at baseline and week 56.
Main Results:
- LV-GLS significantly improved from baseline to week 56 (P=0.02).
- In patients with transient LV ejection fraction reduction, LV-GLS showed no significant worsening.
- RV-GLS (free wall and 4-chamber) remained unchanged, indicating no detrimental effect on RV function.
Conclusions:
- Mavacamten treatment favorably impacts regional LV systolic function, as evidenced by improved LV-GLS.
- The drug demonstrated a favorable safety profile regarding RV systolic function.
- Mavacamten offers a potential therapeutic option for managing oHCM with sustained systolic function benefits.
Background:
In severely symptomatic patients with obstructive hypertrophic cardiomyopathy, VALOR-HCM (A Study to Evaluate Mavacamten in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Who Are Eligible for Septal Reduction Therapy) demonstrated that mavacamten reduces the need for septal reduction therapy with sustained improvement in left ventricular (LV) outflow tract gradients and symptoms. Global longitudinal strain (GLS), a measure of regional myocardial function, is a more sensitive marker of systolic function. In VALOR-HCM, we assessed serial changes in LV and right ventricular (RV) strain.
Methods:
VALOR-HCM included 112 patients with symptomatic obstructive hypertrophic cardiomyopathy (mean, 60 years; 51% male; LV ejection fraction, 68%). Patients assigned to mavacamten at baseline continued the drug for 56 weeks (n=56) and those assigned to placebo (n=52) transitioned to mavacamten from weeks 16 to 56 (40-week exposure). LV-GLS and RV-GLS assessment was performed using a vendor-neutral software. Non-foreshortened apical (4-, 3-, and 2-chamber) views were used to obtain peak LV-GLS. RV focused 4-chamber view was used to calculate RV 4-chamber and free wall strain. A more negative strain value is favorable.
Results:
At baseline, the mean LV-GLS, RV 4-chamber, and free wall strain values were -14.7%, -22.2%, and -16.8%, respectively (all worse than reported normal means). In the total study sample, LV-GLS significantly improved from baseline to week 56 (P=0.02). Twelve patients had transient reduction in LV ejection fraction (<50%) requiring temporary drug interruption (including 3 permanent discontinuations). The LV-GLS in this subgroup was worse at baseline versus total study population (-11.4%), with no significant worsening from baseline through week 56 (P=0.64). Both free wall and 4-chamber RV-GLS remained unchanged from baseline to week 56 (P=0.62 and P=0.56, respectively).
Conclusions:
In VALOR-HCM, treatment with mavacamten improved LV-GLS from baseline through week 56 (with no significant worsening of LV-GLS in patients with a reduction in LV ejection fraction ≤50%), suggesting a favorable long-term impact on regional LV systolic function. Additionally, there was no detrimental impact on RV systolic function.
Registration:
URL: https://www.clinicaltrials.gov; Unique identifier: NCT04349072.
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