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Updated: Mar 14, 2026

Transthoracic Speckle Tracking Echocardiography for the Quantitative Assessment of Left Ventricular Myocardial Deformation
Published on: October 20, 2016
Left ventricular non-compaction and idiopathic dilated cardiomyopathy: the significant diagnostic value of
Fanny Tarando1,2, Damien Coisne3,2, Elena Galli1,4,2
1Service de Cardiologie and CIC-IT 1414, Hôpital Pontchaillou - CHU Rennes, 2 rue Henri Le Guillou, 35000, Rennes, France.
Insights
Left ventricular non-compaction (LVNC) is difficult to distinguish from dilated cardiomyopathy (DCM). A specific mid-wall strain base-apex gradient using echocardiography can help differentiate these conditions.
Area of Science:
- Cardiology
- Medical Imaging
- Biomedical Engineering
Background:
- Left ventricular non-compaction (LVNC) presents with abnormal trabeculations, often challenging to differentiate from dilated cardiomyopathies (DCM).
- Accurate distinction is crucial for appropriate patient management and prognosis.
Purpose of the Study:
- To identify novel echocardiographic tools for differentiating LVNC from DCM.
- To evaluate the diagnostic performance of longitudinal strain characteristics.
Main Methods:
- Compared longitudinal strain patterns in 48 LVNC patients and 45 DCM patients (derivation cohort).
- Analyzed global and regional multi-layer LV longitudinal strain.
- Validated findings in a separate cohort of 41 LVNC patients.
Main Results:
- LVNC patients exhibited greater longitudinal deformation than DCM patients.
- A mid-wall strain base-apex gradient showed 88.4% sensitivity and 66.7% specificity in distinguishing LVNC from DCM.
- This gradient was the sole independent echocardiographic predictor in multivariable analysis.
Conclusions:
- Longitudinal strain, particularly the base-apex gradient, is a valuable additive tool for differentiating LVNC from DCM.
- The findings were confirmed in a validation cohort, demonstrating high sensitivity and negative predictive value.
Abstract:
Left ventricular non-compaction (LV NC) is characterized by abnormal trabeculations that are mainly at the LV apex. Distinction between LV NC and non-specific dilated cardiomyopathies (DCMs) remains often challenging. We sought to find additive tools comparing the longitudinal strain characteristics of LVNC versus idiopathic DCM in a cohort of patients. 48 cases of LVNC (derivation cohort) were compared with 45 cases of DCM. Global and regional multi-layer (sub-endocardial, mid-wall, and sub-epicardial) LV longitudinal strain analysis was performed. Results were compared to define the best tool for distinguishing LVNC from DCM. A validation cohort (41 LVNC patients) was then used to assess the performance of the proposed diagnostic tools. In the derivation cohort, longitudinal deformation (strain) was greater in LVNC than in DCM patients. Longitudinal shortening was greater in the non-compacted segments than in the compacted ones. A mid-wall strain base-apex gradient had 88.4 % sensitivity and 66.7 % specificity in distinguishing LVNC from DCM (AUC = 0.83; cut-off of -23 or |0.23|%). In a multivariable model, the base-apex mid-wall gradient in an apical 4-chamber view was the only independent echocardiographic criteria (OR = 0.76, CI 95 % [0.66; 0.90], p = 0.0010) allowing the distinction between LVNC and DCM. In the validation cohort, the base-apex mid-wall gradient of strain had 88.4 % sensitivity, 85.7 % negative predictive values for the diagnosis of LVNC. Longitudinal strain, especially the base-apex longitudinal gradient of strain, appears as an additive valuable tool for distinguishing LVNC from DCM.
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