Abnormal septal convexity into the left ventricle occurs in subclinical hypertrophic cardiomyopathy

Background: sarcomeric gene mutations cause hypertrophic cardiomyopathy (hcm). in gene mutation carriers without left ventricular (lv) hypertrophy (g + lvh-),subclinical imaging biomarkers are recognized as predictors of overt hcm,consisting of anterior mitral valve leaflet elongation,myocardial crypts,hyperdynamic lv ejection fraction,and abnormal apical trabeculation. reverse curvature of the interventricular septum (into the lv) is characteristic of overt hcm. we aimed to assess lv septal convexity in subclinical hcm. methods: cardiovascular magnetic resonance was performed on 36 g + lvh- individuals (31 ± 14 years,33 % males) with a pathogenic sarcomere mutation,and 36 sex and age-matched healthy controls (33 ± 12 years,33 % males). septal convexity (scx) was measured in the apical four chamber view perpendicular to a reference line connecting the mid-septal wall at tricuspid valve insertion level and the apical right ventricular insertion point. results: septal convexity was increased in g + lvh- compared to controls (maximal distance of endocardium to reference line: 5.0 ± 2.5 mm vs. 1.6 ± 2.4 mm,p ≤ 0.0001). expected findings occurred in g + lvh- individuals: longer anterior mitral valve leaflet (23.5 ± 3.0 mm vs. 19.9 ± 3.1 mm,p ≤ 0.0001),higher relative wall thickness (0.31 ± 0.05 vs. 0.29 ± 0.04,p ≤ 0.05),higher lv ejection fraction (70.8 ± 4.3 % vs. 68.3 ± 4.4 %,p ≤ 0.05),and smaller lv end-systolic volume index (21.4 ± 4.4 ml/m2 vs. 23.7 ± 5.8 ml/m2,p ≤ 0.05). other morphologic measurements (lv angles,sphericity index,and eccentricity index) were not different between g + lvh- and controls. conclusions: septal convexity is an additional previously undescribed feature of subclinical hcm. © 2015 reant et al.