European Heart Journal · 2005 · 14 citations · 25 references
MedicineCardiologyInternal MedicineCardiovascular GeneticsClinical CardiologyMedical GeneticsCardiac AssessmentCardiac ImagingCardiovascular AssessmentCardiovascular DiseaseHypertrophic Cardiomyopathy GeneticsLeft Ventricular Function AssessmentCardiomyopathy Genotype-phenotype CorrelationDiagnostic Accuracy StudiesDiagnostic Testing AccuracyEchocardiographic PhenotypingLeft Ventricular Hypertrophy CriteriaLeft Ventricular Wall Thickness AssessmentReceiver Operating Characteristic AnalysisSensitivity
AIMS: To study the diagnostic value of a new 2D left ventricle hypertrophy (2D LVH) score in families with hypertrophic cardiomyopathy (HCM) in comparison with the conventional maximal wall thickness (MWT) measurement (>13 mm in adults), which is limited by a low sensitivity in relatives. METHODS AND RESULTS: The study was performed in 237 adults from genotyped families with HCM. Population A (derivation sample) comprised 109 adults and population B (validation sample) comprised 128 adults. MWT and 2D LVH scores (sum of thicknesses of four segments) were determined by echocardiography. Genotyping was the gold standard for diagnosis. In population A, a theoretical value for LVH score was determined in the healthy population by a multiple linear regression model including age, sex, and body surface area. An abnormal cut-off value was defined as an LVH score above a maximum theoretical value according to receiver operating characteristic analysis. Sensitivity and specificity were, respectively, 73 and 96% for 2D LVH score and 62.5 and 100% for MWT. Improvement of sensitivity was particularly important in adults <50 years of age (69 vs. 54%, respectively, P<0.04). These results were validated in population B: sensitivity and specificity of LVH score were, respectively, 75 and 96% in this sample and 67 and 97%, in the subgroup <50 years. In the latter, sensitivity of LVH score increased when compared with that of MWT (67 vs. 53%, P<0.03). CONCLUSIONS: The LVH score has a higher diagnostic value for HCM than the conventional criterion of MWT, particularly in young adults. This echographic parameter may be proposed as an alternative diagnostic criterion for familial screening.
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Anja A. T. Geisterfer-Lowrance, Michael E. Christe, David A. Conner et al. · Science · 1996 · 556 citations
Medicine, Cardiology, Genetics +10