Anterior mitral valve leaflet length and response to mavacamten in obstructive hypertrophic cardiomyopathy

This study examines whether anterior mitral valve leaflet (AMVL) length is associated with response to mavacamten in patients with obstructive hypertrophic cardiomyopathy (HCM). Obstruction of the left-ventricular outflow tract (LVOT) in HCM has been associated with asymmetric septal hypertrophy and...

Full description

Saved in:
Bibliographic Details
Published inEuropean heart journal. Imaging methods and practice Vol. 3; no. 2; p. qyaf081
Main Authors Saleh, Danish, Kim, Ellis Y, Hussain, Kifah, Appadurai, Vinesh, Mueller, Kayla, Garza, Abigail, Cheema, Baljash, Fullenkamp, Dominic E, Rigolin, Vera H, Narang, Akhil, Cremer, Paul C, Choudhury, Lubna
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.07.2025
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:This study examines whether anterior mitral valve leaflet (AMVL) length is associated with response to mavacamten in patients with obstructive hypertrophic cardiomyopathy (HCM). Obstruction of the left-ventricular outflow tract (LVOT) in HCM has been associated with asymmetric septal hypertrophy and abnormalities of the mitral valve and sub-valvular apparatus. Mavacamten is a myosin-inhibitor shown to decrease LVOT gradient and improve functional status in patients with obstructive HCM. Measurements of cardiac structural elements were obtained from magnetic resonance imaging and echocardiography data among patients with obstructive HCM treated with mavacamten. Endpoints were effective mavacamten dose, defined as the dose required to achieve a Valsalva LVOT gradient <30 mmHg, and rapid response to mavacamten therapy, defined as achieved Valsalva LVOT gradient <20 mmHg within 8 weeks of initiation. Among 33 patients, patients with an effective dose of 5 mg ( = 13) had a shorter AMVL length [20.00 (18.50, 20.80) mm] compared with patients with a dose of 10 mg ( = 12) [23.30 (22.45, 26.10) mm] and 15 mg ( = 8) [25.45 (24.20, 26.85) mm] ( < 0.001). After adjusting for age and sex, the 5 mg dose was associated with a shorter AMVL length ( = 0.003). AMVL length was shorter in rapid responders [20.9 (19.9, 22.5) mm] compared with patients without a rapid response [24.9 (23.3, 26.5) mm] ( = 0.006). Shorter AMVL length is associated with a lower effective dose and a rapid response to mavacamten. If confirmed in larger studies, AMVL length may inform optimal dosing of myosin inhibitors in obstructive HCM.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Conflict of interest: B.C. has served as a consultant for Caption Health, Inc and Viz.ai; speaker with honorarium from BMS; has served on an Advisory Board for Novo Nordisk; and is an advisor with equity interest in Healthspan, Inc and Zoe Biosciences. V.H.R. has stock ownership in BMS. A.N. has served as a speaker with honorarium from Abbott, Bristol Meyers Squibb, and Edwards Lifesciences. P.C.C. reported receiving grants from Novartis and Kiniksa and receiving personal fees from Kiniksa, Sobi, and CardiolRx Therapeutics outside the submitted work. L.C. co-authored the EXPLORER-HCM study of Mavacamten in obstructive HCM and the MAVERICK-HCM study on non-obstructive HCM; she is an investigator of the MAVA-LTE study examining the long-term effects of Mavacamten in obstructive and non-obstructive HCM.
ISSN:2755-9637
2755-9637
DOI:10.1093/ehjimp/qyaf081