Tissue Doppler Imaging and Plasma N-Terminal Probrain Natriuretic Peptide for the Identification of Hypertrophic Cardiomyopathy Mutation Carriers

• Published in: The American journal of cardiology 2013-10, Vol.112 (7), p.996-1004
• Main Authors: Silva, Doroteia, MD, Madeira, Hugo, MD, PhD, Almeida, Augusto, MSc, Brito, Dulce, MD, PhD
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Age; Aged; Aged, 80 and over; Cardiomyopathy, Hypertrophic - diagnosis; Cardiomyopathy, Hypertrophic - genetics; Cardiovascular; Child; Child, Preschool; Echocardiography, Doppler; Female; Genetic counseling; Genotype; Heterozygote; Humans; Male; Middle Aged; Mutation; Myosins - genetics; Natriuretic Peptide, Brain - blood; Patients; Peptide Fragments - blood; Plasma; Prospective Studies; Studies; Troponin - genetics; Young Adult
• ISSN: 0002-9149; 1879-1913
• DOI: 10.1016/j.amjcard.2013.05.039

Previous studies have shown that tissue Doppler imaging (TDI) is able to identify mutation carriers of hypertrophic cardiomyopathy (HC) before the development of the clinical phenotype. However, data are scarce and have sometimes been controversial. We performed a systematic study that included conventional echocardiography, TDI, and plasma NT-probrain natriuretic peptide (NT-proBNP) measurement to evaluate the parameters that could identify HC mutation carriers. A total of 138 genotyped subjects were included and divided into 3 groups: group 1, those with HC (n = 62); group 2, mutation carriers (first-degree relatives with a positive genotype but negative phenotype; n = 34); and group 3, controls (first-degree relatives with a negative genotype and phenotype; n = 42). An echocardiographic study, including TDI, was performed on all subjects, and a TDI-derived index (global function index) was also determined. The age-adjusted mean differences in the echocardiographic and TDI parameters and NT-proBNP levels were compared among the 3 groups. Compared with the HC group, the carriers had significantly higher mean E′ velocities, lower mean E/E′ ratio, higher mean S′ velocities, and lower mean global function index and NT-proBNP values. The carriers and controls did not differ significantly either in the echocardiographic parameters studied or in the NT-proBNP levels. In conclusion, the echocardiographic and TDI parameters and NT-proBNP levels cannot be used to identify the HC mutation carrier state and therefore do not appear to be reliable for the purpose of making a preclinical diagnosis of the disease.