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Published on: June 14, 2016
In patients with hypertrophic cardiomyopathy myocardial fibrosis is associated with both left ventricular and left
Christian Prinz1, Frank Van Buuren, Nicola Bogunovic
1Dept. of Cardiology, Heart and Diabetes Centre North-Rhine Westphalia, Ruhr University Bochum, Bad Oeynhausen, Germany. Cchrprinz@aol.com
Insights
Myocardial fibrosis in hypertrophic cardiomyopathy is linked to impaired left atrial and ventricular function. This dysfunction correlates with more severe heart failure symptoms, highlighting fibrosis as a key indicator of disease progression.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Cardiac Physiology
Background:
- Hypertrophic cardiomyopathy (HCM) is a genetic heart muscle disease characterized by left ventricular hypertrophy.
- Myocardial fibrosis, the deposition of collagen in the heart muscle, is a common finding in HCM and is associated with adverse outcomes.
- Left atrial (LA) function plays a crucial role in diastolic filling and overall cardiac performance.
Purpose of the Study:
- To evaluate left atrial (LA) function using two-dimensional speckle-tracking echocardiography (2DSTE).
- To investigate the relationship between LA function and myocardial fibrosis in patients with hypertrophic cardiomyopathy (HCM).
Main Methods:
- 30 HCM patients underwent 2DSTE to assess global longitudinal left ventricular (LV) strain and LA strain/strain-rate parameters.
- Delayed-enhancement magnetic resonance imaging (DE-MRI) was used to detect and quantify myocardial fibrosis.
- Patients were categorized into two groups: no fibrosis and moderate-to-severe fibrosis in at least two LV segments.
Main Results:
- 20 patients (66.7%) exhibited moderate or severe myocardial fibrosis.
- Patients with fibrosis showed significantly reduced global longitudinal LV strain and peak LA strain compared to those without fibrosis.
- Increased indexed LA volume and higher New York Heart Association (NYHA) class were observed in patients with significant fibrosis, correlating with impaired LA and LV function.
Conclusions:
- Myocardial fibrosis in HCM is associated with impaired left atrial and left ventricular function.
- The presence and extent of fibrosis correlate with the severity of heart failure symptoms (NYHA class).
- 2DSTE is a valuable tool for assessing LA dysfunction in the context of HCM-related myocardial fibrosis.
Aims:
The aim of this study was to assess LA function by two-dimensional speckle-tracking echocardiography and its relation with myocardial fibrosis in hypertrophic cardiomyopathy (HCM).
Methods:
We enrolled 30 consecutive HCM-patients in our study (20 males; age: 49.7 +/- 10.4 years, NYHA-class: 1.9 +/- 0.7). Echocardiography was performed with assessment of global longitudinal LV strain (epsilon) and LA epsilon and strain-rate parameters (systolic, early diastolic, and late diastolic during atrial contraction). Each patient received delayed-enhancement magnetic resonance imaging (DE-MRI) to check for myocardial fibrosis. We divided the patients into two groups. Patients of group 1 had no fibrosis, group 2 demonstrated moderate or severe fibrosis in > or = 2 segments using a 17 segment-model of the LV.
Results:
Moderate and severe fibrosis was observed in 20 patients (group 2: 66.7%). Global longitudinal LV epsilon (-13.0 +/- 2.4 vs -20.6 +/- 3.2%, P < 0.001) and peak LA epsilon (-0.2 +/- 3.9 vs 17.9 +/- 6.7%, P < 0.001) were reduced in group 2 in comparison with patients without myocardial fibrosis. In all patients peak LA epsilon correlated with global longitudinal LV epsilon (r = -0.78, P < 0.001). Patients with considerable myocardial fibrosis (group 2) had a higher indexed left atrial volume (35.7 +/- 12.8 ml/m2 vs 24.1 +/- 8.6 ml/m2, P = 0.016). New York Heart Association class (NYHA) was higher in patients with severe myocardial fibrosis (2.2 +/- 0.7 vs 1.3 +/- 0.5) and correlated with peak LA (r = -0.5, P = 0.008) and global LV epsilon (r = 0.5, P = 0.005).
Conclusions:
Occurrence of myocardial fibrosis in hypertrophic cardiomyopathy is associated with left atrial and ventricular dysfunction as well as with the severity of heart failure symptoms.
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