Left Ventricular Noncompaction: A Distinct Genetic Cardiomyopathy?

Left ventricular noncompaction (LVNC) describes a ventricular wall anatomy characterized by prominent left ventricular (LV) trabeculae, a thin compacted layer, and deep intertrabecular recesses. Individual variability is extreme, and trabeculae represent a sort of individual "cardioprinting.&qu...

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Published inJournal of the American College of Cardiology Vol. 68; no. 9; pp. 949 - 966
Main Authors Arbustini, Eloisa, Favalli, Valentina, Narula, Nupoor, Serio, Alessandra, Grasso, Maurizia
Format Journal Article
LanguageEnglish
Published United States Elsevier Limited 30.08.2016
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ISSN0735-1097
1558-3597
1558-3597
DOI10.1016/j.jacc.2016.05.096

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Abstract Left ventricular noncompaction (LVNC) describes a ventricular wall anatomy characterized by prominent left ventricular (LV) trabeculae, a thin compacted layer, and deep intertrabecular recesses. Individual variability is extreme, and trabeculae represent a sort of individual "cardioprinting." By itself, the diagnosis of LVNC does not coincide with that of a "cardiomyopathy" because it can be observed in healthy subjects with normal LV size and function, and it can be acquired and is reversible. Rarely, LVNC is intrinsically part of a cardiomyopathy; the paradigmatic examples are infantile tafazzinopathies. When associated with LV dilation and dysfunction, hypertrophy, or congenital heart disease, the genetic cause may overlap. The prevalence of LVNC in healthy athletes, its possible reversibility, and increasing diagnosis in healthy subjects suggests cautious use of the term LVNC cardiomyopathy, which describes the morphology but not the functional profile of the cardiomyopathy.
AbstractList Left ventricular noncompaction (LVNC) describes a ventricular wall anatomy characterized by prominent left ventricular (LV) trabeculae, a thin compacted layer, and deep intertrabecular recesses. Individual variability is extreme, and trabeculae represent a sort of individual "cardioprinting." By itself, the diagnosis of LVNC does not coincide with that of a "cardiomyopathy" because it can be observed in healthy subjects with normal LV size and function, and it can be acquired and is reversible. Rarely, LVNC is intrinsically part of a cardiomyopathy; the paradigmatic examples are infantile tafazzinopathies. When associated with LV dilation and dysfunction, hypertrophy, or congenital heart disease, the genetic cause may overlap. The prevalence of LVNC in healthy athletes, its possible reversibility, and increasing diagnosis in healthy subjects suggests cautious use of the term LVNC cardiomyopathy, which describes the morphology but not the functional profile of the cardiomyopathy.Left ventricular noncompaction (LVNC) describes a ventricular wall anatomy characterized by prominent left ventricular (LV) trabeculae, a thin compacted layer, and deep intertrabecular recesses. Individual variability is extreme, and trabeculae represent a sort of individual "cardioprinting." By itself, the diagnosis of LVNC does not coincide with that of a "cardiomyopathy" because it can be observed in healthy subjects with normal LV size and function, and it can be acquired and is reversible. Rarely, LVNC is intrinsically part of a cardiomyopathy; the paradigmatic examples are infantile tafazzinopathies. When associated with LV dilation and dysfunction, hypertrophy, or congenital heart disease, the genetic cause may overlap. The prevalence of LVNC in healthy athletes, its possible reversibility, and increasing diagnosis in healthy subjects suggests cautious use of the term LVNC cardiomyopathy, which describes the morphology but not the functional profile of the cardiomyopathy.
Left ventricular noncompaction (LVNC) describes a ventricular wall anatomy characterized by prominent left ventricular (LV) trabeculae, a thin compacted layer, and deep intertrabecular recesses. Individual variability is extreme, and trabeculae represent a sort of individual "cardioprinting." By itself, the diagnosis of LVNC does not coincide with that of a "cardiomyopathy" because it can be observed in healthy subjects with normal LV size and function, and it can be acquired and is reversible. Rarely, LVNC is intrinsically part of a cardiomyopathy; the paradigmatic examples are infantile tafazzinopathies. When associated with LV dilation and dysfunction, hypertrophy, or congenital heart disease, the genetic cause may overlap. The prevalence of LVNC in healthy athletes, its possible reversibility, and increasing diagnosis in healthy subjects suggests cautious use of the term LVNC cardiomyopathy, which describes the morphology but not the functional profile of the cardiomyopathy.
Author Arbustini, Eloisa
Favalli, Valentina
Serio, Alessandra
Narula, Nupoor
Grasso, Maurizia
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Keywords genetic counseling
congenital heart disease
heart ventricles
myocardium
mitochondrial myopathies
genetic testing
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References 27737754 - J Am Coll Cardiol. 2016 Oct 18;68(16):1821
28254188 - J Am Coll Cardiol. 2017 Mar 7;69(9):1209-1210
28254189 - J Am Coll Cardiol. 2017 Mar 7;69(9):1210-1211
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Snippet Left ventricular noncompaction (LVNC) describes a ventricular wall anatomy characterized by prominent left ventricular (LV) trabeculae, a thin compacted layer,...
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StartPage 949
SubjectTerms Athletes
Blood diseases
Cardiac arrhythmia
Cardiology
Cardiomyopathies - diagnosis
Cardiomyopathies - genetics
Cardiomyopathies - physiopathology
Cardiomyopathy
Cardiovascular disease
Congenital diseases
Diagnosis, Differential
Family medical history
Genetic counseling
Genetic Testing
Heart
Humans
Hypotheses
Isolated Noncompaction of the Ventricular Myocardium - diagnosis
Isolated Noncompaction of the Ventricular Myocardium - genetics
Isolated Noncompaction of the Ventricular Myocardium - physiopathology
Medical imaging
Morphology
Ratios
Ventricular Function, Left - physiology
Title Left Ventricular Noncompaction: A Distinct Genetic Cardiomyopathy?
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