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Published on: October 28, 2020
Left Ventricular Noncompaction: Anatomical Phenotype or Distinct Cardiomyopathy?
Jonathan R Weir-McCall1, Phey Ming Yeap1, Carla Papagiorcopulo1
1Department of Cardiovascular and Diabetes Medicine, College of Medicine, University of Dundee, Dundee, United Kingdom.
Left ventricular noncompaction (LVNC) criteria are met by a significant portion of healthy individuals, questioning if LVNC is a distinct disease or an anatomical variation. This study highlights poor specificity in current diagnostic methods for LVNC.
Area of Science:
- Cardiology
- Medical Imaging
- Pathology
Background:
- Left ventricular noncompaction (LVNC) shows significant overlap with other cardiomyopathies.
- Its high prevalence in the general population (up to 40%) challenges its classification as a distinct pathological entity.
- Questions arise whether LVNC is a pathological entity, a remodeling epiphenomenon, or an anatomical phenotype.
Purpose of the Study:
- To determine the prevalence and predictors of LVNC in a healthy population.
- To evaluate the diagnostic performance of four cardiac magnetic resonance imaging (CMR) criteria for LVNC.
- To investigate the specificity of current LVNC diagnostic criteria in an asymptomatic cohort.
Main Methods:
- 1,651 volunteers over 40 without cardiovascular disease (CVD) underwent CMR.
- Four diagnostic criteria for LVNC were applied, including noncompaction ratios and myocardial mass ratios.
- Participants meeting all four criteria were classified as having LVNC.
Main Results:
- Of 1,480 analyzed participants, 1.3% met all four diagnostic criteria for LVNC.
- 14.8% met at least one criterion, indicating low specificity of current diagnostic methods.
- The noncompacted to compacted myocardial mass ratio was the most specific criterion (4.4%).
Conclusions:
- A substantial proportion of asymptomatic individuals without CVD meet current CMR diagnostic criteria for LVNC.
- This suggests that current criteria have poor specificity for diagnosing LVNC.
- LVNC may represent an anatomical phenotype rather than a distinct cardiomyopathy.
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