Why the septum thickens in hypertrophic cardiomyopathy

In hypertrophic cardiomyopathy (HCM), hypertrophy often disproportionately affects the interventricular septum, especially in the obstructive form (oHCM). The reasons for this septal predilection remain debated. Here, we review emerging evidence that septal hypertrophy in HCM represents a localised, load-driven remodelling response, an adaptive "retrofitting" of the heart's wall to withstand abnormal stress. Congenital differences in septal fibre architecture and chronic sarcomeric hypercontractility create a focal mechanical burden that predisposes the septum to near-isometric contraction (low septal mobility) and drives early hypertrophic remodelling. When present, systolic anterior motion of the mitral valve and left ventricular (LV) outflow tract obstruction (LVOTO) further amplify this load, increase wall stress, and accelerate this process. Analogous to earthquake engineering, where rigid buildings are retrofitted with dampers to absorb shocks, the septum adapts by accumulating viscoelastic elements (e.g., microtubules, titin, collagen) that thicken and stiffen the wall. This structural adaptation protects against further damage by limiting myocardial shortening and reducing wall tension (according to Laplace's law), albeit at the cost of diastolic dysfunction and energetic inefficiency. We integrate haemodynamic studies and new patient-specific computational modelling data to confirm this load-centric model. When LVOTO develops, the added external load activates the afterload-dependent compensation (Anrep effect), characterised by increased LV end-systolic pressure, enhanced contractility, prolonged ejection, and elevated myocardial work. Septal reduction (surgery/ablation) relieves the external load imposed by LVOTO, whereas myosin inhibition (mavacamten) reduces the internal load from sarcomere-level hypercontractility and can secondarily lessen dynamic obstruction. Both approaches therefore reduce septal stress (although not equally), but myosin inhibition acts earlier in the disease sequence. Computational models further demonstrate that removing the septal load yields a more homogeneous stress distribution and improves mechano-energetic efficiency in the ventricle. Thus, septal hypertrophy in HCM is best understood as a targeted, load-driven remodelling analogous to structural retrofitting. Reducing sarcomere-level hypercontractility and, when present, the added load from LVOTO addresses the key mechanical drivers of disease, halting the maladaptive cycle and potentially allowing reverse remodelling. This unifying framework, now corroborated by computational modelling, positions ventricular unloading as a central therapeutic strategy in HCM.

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Publication Details

Journal
Journal of Molecular and Cellular Cardiology Plus
Published
2026-04-22
DOI
https://doi.org/10.1016/j.jmccpl.2026.100849
Primary Topic
Cardiomyopathy and Myosin Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Why the septum thickens in hypertrophic cardiomyopathy

Jan M. Federspiel, Vasco Sequeira, Jan‐Christian Reil
Journal of Molecular and Cellular Cardiology Plus
Cardiomyopathy and Myosin Studies
article

Why the septum thickens in hypertrophic cardiomyopathy

Jan M. Federspiel, Vasco Sequeira, Jan‐Christian Reil
article en

Abstract

In hypertrophic cardiomyopathy (HCM), hypertrophy often disproportionately affects the interventricular septum, especially in the obstructive form (oHCM). The reasons for this septal predilection remain debated. Here, we review emerging evidence that septal hypertrophy in HCM represents a localised, load-driven remodelling response, an adaptive "retrofitting" of the heart's wall to withstand abnormal stress. Congenital differences in septal fibre architecture and chronic sarcomeric hypercontractility create a focal mechanical burden that predisposes the septum to near-isometric contraction (low septal mobility) and drives early hypertrophic remodelling. When present, systolic anterior motion of the mitral valve and left ventricular (LV) outflow tract obstruction (LVOTO) further amplify this load, increase wall stress, and accelerate this process. Analogous to earthquake engineering, where rigid buildings are retrofitted with dampers to absorb shocks, the septum adapts by accumulating viscoelastic elements (e.g., microtubules, titin, collagen) that thicken and stiffen the wall. This structural adaptation protects against further damage by limiting myocardial shortening and reducing wall tension (according to Laplace's law), albeit at the cost of diastolic dysfunction and energetic inefficiency. We integrate haemodynamic studies and new patient-specific computational modelling data to confirm this load-centric model. When LVOTO develops, the added external load activates the afterload-dependent compensation (Anrep effect), characterised by increased LV end-systolic pressure, enhanced contractility, prolonged ejection, and elevated myocardial work. Septal reduction (surgery/ablation) relieves the external load imposed by LVOTO, whereas myosin inhibition (mavacamten) reduces the internal load from sarcomere-level hypercontractility and can secondarily lessen dynamic obstruction. Both approaches therefore reduce septal stress (although not equally), but myosin inhibition acts earlier in the disease sequence. Computational models further demonstrate that removing the septal load yields a more homogeneous stress distribution and improves mechano-energetic efficiency in the ventricle. Thus, septal hypertrophy in HCM is best understood as a targeted, load-driven remodelling analogous to structural retrofitting. Reducing sarcomere-level hypercontractility and, when present, the added load from LVOTO addresses the key mechanical drivers of disease, halting the maladaptive cycle and potentially allowing reverse remodelling. This unifying framework, now corroborated by computational modelling, positions ventricular unloading as a central therapeutic strategy in HCM.

Journal of Molecular and Cellular Cardiology PlusVol. 16
University of Würzburg (DE), Heart and Diabetes Center North Rhine-Westphalia (DE), Comprehensive Cancer Center Mainfranken (DE), Universitätsklinikum Würzburg (DE), Saarland University (DE)
Bristol-Myers Squibb, Deutsche Forschungsgemeinschaft, Julius-Maximilians-Universität Würzburg
Sustainable cities and communities
Openalex Percentile: Top 18%
Cardiomyopathy and Myosin Studies
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