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Published on: June 14, 2016
Two types of left ventricular wall motion abnormalities with distinct clinical features in patients with hypertrophic
S Ishiwata1, S Nishiyama, S Nakanishi
1Cardiovascular Center, Toranomon Hospital, Tokyo, Japan.
Insights
Hypertrophic cardiomyopathy (HCM) patients can develop left ventricular (LV) wall motion abnormalities. Two distinct patterns emerged, suggesting different underlying mechanisms for these HCM complications.
Area of Science:
- Cardiology
- Cardiovascular Research
- Medical Science
Background:
- Hypertrophic cardiomyopathy (HCM) can lead to left ventricular (LV) wall motion abnormalities.
- These abnormalities may develop over time without coronary artery disease.
- Understanding predictors and mechanisms is crucial for patient management.
Purpose of the Study:
- To investigate the incidence, mechanisms, and predictors of LV wall motion abnormalities in HCM patients.
- To identify clinical features influencing the gradual development of these abnormalities.
- To differentiate between distinct patterns of LV dysfunction in long-term HCM follow-up.
Main Methods:
- Retrospective analysis of 162 HCM patients with an average follow-up of 13.3 years.
- Focused on 16 patients who developed LV wall motion abnormalities.
- Categorized abnormalities into apical segmental dysfunction with obstruction and generalized hypokinesis.
Main Results:
- Two distinct patterns of LV wall motion abnormalities were identified.
- 11 patients showed apical dysfunction with midzone obstruction, linked to extensive apical hypertrophy.
- Five patients developed generalized hypokinesis, with initial LV contractility decrease.
Conclusions:
- HCM patients can develop distinct forms of LV wall motion abnormalities.
- Apical hypertrophy and initial LV dysfunction predict different abnormality patterns.
- These patterns suggest different underlying pathophysiological mechanisms in HCM progression.
Abstract:
During the long-term follow-up of patients with hypertrophic cardiomyopathy (HCM), some patients develop left ventricular (LV) wall motion abnormalities in the absence of fixed coronary artery disease. The purpose of this study is to clarify which clinical features in patients with HCM seem to influence gradual development of LV wall motion abnormalities over an extended period of time. The study investigates the incidence, mechanism and predictors of these abnormalities. In this retrospective study of 162 patients with HCM, followed-up for an average of 13.3 years, we focused our attention on 16 patients who gradually developed two different forms of LV wall motion abnormality. In 11 of these 16 patients, apical segmental dysfunction with midzone obstruction was recognized; the remaining five patients showed generalized hypokinesis, as seen in dilated cardiomyopathy. The 11 patients with apical segmental dysfunction presented with extensive apical hypertrophy reaching the midventricular level at first examination. The five patients with generalized hypokinesis showed a slight decrease in LV contractility and reduced localized antero-apical wall motion even at initial examination. None of the patients in either group developed the other group's features during their clinical course. These two groups had different initial manifestations and pursued different clinical courses, suggesting that the underlying mechanisms causing wall motion abnormalities are different.
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