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Updated: May 25, 2026

Evaluation of Left Ventricular Structure and Function using 3D Echocardiography
Published on: October 28, 2020
Isolated left ventricular noncompaction in sub-Saharan Africa: a clinical and echocardiographic perspective
Ferande Peters1, Bijoy K Khandheria, Claudia dos Santos
1Department of Cardiology, Chris Hani Baragwanath Hospital, University of the Witwatersrand, Johannesburg, South Africa.
Insights
Isolated left ventricular noncompaction (ILVNC) in Africans often involves both ventricles and is linked to pulmonary hypertension. This study highlights key echocardiographic features in this population.
Area of Science:
- Cardiology
- Medical Imaging
- Genetics
Background:
- Isolated left ventricular noncompaction (ILVNC) is a rare cardiomyopathy.
- It results from impaired fetal myocardial compaction, leading to heart failure, arrhythmias, and cardioembolism.
- Limited data exists on ILVNC's clinical and echocardiographic profile in African populations.
Purpose of the Study:
- To investigate the clinical and echocardiographic characteristics of ILVNC in African patients.
- To identify specific features of ILVNC in this demographic.
- To compare findings with healthy controls of African descent.
Main Methods:
- A single-center, prospective case-control study.
- Screening and diagnosis of ILVNC based on specific echocardiographic criteria (LVNC ratio >2, apical trabeculations >3, deep intertrabecular recesses).
- Inclusion of 54 ILVNC patients and a control group of African descent.
Main Results:
- The prevalence of ILVNC in the cardiomyopathy clinic was 6.9%.
- Heart failure with systolic dysfunction (98.1%) was the primary presentation, with reduced ejection fraction (26.7±11.9%).
- Biventricular abnormalities (right ventricular noncompaction in 22.2%, dilation in 74.1%, depressed function in 59.3%) and pulmonary hypertension (83.3%) were common.
Conclusions:
- ILVNC in patients of African descent frequently presents with biventricular abnormalities.
- Pulmonary hypertension is a significant associated finding.
- These findings expand the understanding of ILVNC beyond isolated left ventricular involvement.
Background:
Isolated left ventricular noncompaction (ILVNC) is a cardiomyopathy caused by intrauterine failure of the myocardium to compact. Common clinical complications are heart failure, arrhythmias, and cardioembolism. A paucity of data exists relating to clinical and echocardiographic features of ILVNC in Africans.
Methods And Results:
This study is a single-center, prospective case-control study, whereby subjects attending a dedicated cardiomyopathy clinic were screened for and diagnosed with ILVNC, provided they had no other associated structural heart disease and fulfilled all the accompanying echocardiographic criteria: (1) end-systolic ratio of noncompacted layer to compacted layer >2, (2) presence of >3 prominent apical trabeculations, and (3) deep intertrabecular recesses that fill with blood from the ventricular cavity visualized using color Doppler ultrasound. Fifty-four subjects were identified, age 45.4±13.1 years (mean±SD), 95% confidence interval 3.6 to 10.2, 55.6% male, and 63.0% New York Health Association Class II, and prevalence of LVNC in our clinic was 6.9%, 95% confidence interval 3.6 to 10.2. Heart failure because of systolic dysfunction was the most common clinical presentation (53 subjects, 98.1%). Left ventricular end-diastolic diameter was 61.4±7.2 mm (mean±SD) and ejection fraction 26.7±11.9% (mean±SD). Common sites of noncompaction were the apical (100%), midinferior (74.1%), and midlateral (64.8%) walls. Right ventricular noncompaction occurred in 12 subjects (22.2%). Pulmonary hypertension was documented in 45 cases (83.3%). Right ventricular dilation was noted in 40 subjects (74.1%), while right ventricular function was depressed in 32 (59.3%). Tricuspid S' was 9.6±2.8 cm/s (mean±SD). No echocardiographic features suggestive of ILVNC were noted in a healthy control group of African descent.
Conclusions:
ILVNC in patients of African descent can be characterized by biventricular abnormality and pulmonary hypertension, in addition to isolated left-sided abnormality.
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