Key result
LVH patterns differentiate myocardial strain, with pattern 2 linked to severe LVGLS impairment.
Why the study?
The impact of different left ventricular hypertrophy distribution patterns on myocardial strain and atrioventricular coupling in hypertrophic cardiomyopathy remains unclear.
How do different left ventricular hypertrophy distribution patterns and obstruction impact myocardial strain and left atrioventricular coupling in patients with hypertrophic cardiomyopathy?
Observational (n=199)
How do different left ventricular hypertrophy distribution patterns and obstruction impact myocardial strain and left atrioventricular coupling in patients with hypertrophic cardiomyopathy?
Effect estimate: β=2.14
p-value: p=0.007
Different LVH patterns in HCM significantly impact myocardial strain on cardiac MRI, with septal plus other segment hypertrophy showing the most severe longitudinal strain impairment.
Different LVH patterns may alter strain and atrioventricular coupling in HCM; leaves open clinical relevance and need for prospective validation.
BACKGROUND: Hypertrophic cardiomyopathy (HCM) exhibits complex phenotypic heterogeneity. Left ventricular myocardial strain and atrioventricular coupling hold significant clinical value in cardiovascular diseases; however, the impact of different left ventricular hypertrophy (LVH) distribution patterns on myocardial strain and atrioventricular coupling remains unclear in HCM. OBJECTIVE: To investigate left ventricular strain and left atrioventricular coupling in HCM patients with different LVH distribution patterns and obstruction using cardiac magnetic resonance feature tracking. METHODS: A total of 199 HCM patients were divided into four LVH patterns (P1-P4): P1 (isolated septal hypertrophy), P2 (septal+other segments hypertrophy, non-apical), P3 (apical+other segments hypertrophy) and P4 (isolated apical hypertrophy). We measured left ventricular global longitudinal strain (LVGLS), global radial strain (LVGRS), global circumferential strain (LVGCS) and left atrioventricular coupling index (LACI). Parameters were compared across groups and between obstructive HCM (HOCM) and non-obstructive HCM (HNCM). RESULTS: Strain differed significantly among the four groups (all p<0.05). LVGLS impairment was most severe in P2. P4 showed better LVGRS and LVGCS than the other groups. Absolute LVGRS and LVGCS were higher in HOCM than HNCM (both p<0.05), but LVGLS did not differ. However, after indexing LVGRS to left ventricular maximal wall thickness (LVMWT) (LVGRS/LVMWT), the difference between HOCM and HNCM was no longer significant (p=0.999). HOCM also had higher LACI, left atrial volumes (all p<0.05). On multivariable analysis, P2 was independently associated with LVGLS impairment (β=2.14, adjusted p=0.007). P4 was independently associated with better LVGRS and LVGCS (adjusted p<0.05). Obstruction was independently associated with LVGCS (adjusted p<0.05). LACI showed no independent association with hypertrophy pattern or obstruction (all adjusted p>0.05). CONCLUSION: LVH patterns on cardiac MR effectively differentiate myocardial strain in HCM. P2 identifies a subtype with severe LVGLS impairment, whereas P4 shows preserved LVGRS and LVGCS. Obstruction independently correlates with compensatory enhancement of LVGCS with larger left atrial volumes, whereas the augmentation of LVGRS may be attributable to wall thickness differences. LACI is not independently associated with LVH pattern or obstruction.
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Li et al. (2026) conducted an observational in Hypertrophic cardiomyopathy (n=199). Left ventricular hypertrophy distribution patterns and obstruction vs. Comparison among different patterns (P1-P4) and non-obstructive HCM was evaluated on Left ventricular global longitudinal strain (LVGLS), global radial strain (LVGRS), global circumferential strain (LVGCS) and left atrioventricular coupling index (LACI) (β=2.14, p=0.007). Left ventricular hypertrophy patterns effectively differentiate myocardial strain, with pattern 2 independently associated with severe LVGLS impairment (β=2.14, p=0.007).
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