Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0036115
Title: Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers
Authors: Yiu K.H.
Atsma D.E.
Delgado V.
Ng A.C.T.
Witkowski T.G.
Ewe S.H. 
Auger D.
Holman E.R.
van Mil A.M.
Breuning M.H.
Tse H.F.
Bax J.J.
Schalij M.J.
Marsan N.A.
Keywords: angiotensin receptor antagonist
beta adrenergic receptor blocking agent
calcium channel blocking agent
dipeptidyl carboxypeptidase inhibitor
diuretic agent
myosin binding protein C
adult
article
calibration
cardiovascular risk
clinical article
controlled study
coronary artery disease
diabetes mellitus
electrocardiogram
female
gene mutation
heart ejection fraction
heart infarction
heart left ventricle
heart muscle
heart muscle revascularization
heart ventricle wall motion
heterozygote detection
human
hyperlipidemia
hypertension
hypertrophic cardiomyopathy
kidney dysfunction
male
phenotype
protein expression
reproducibility
sensitivity and specificity
smoking
systolic dysfunction
echocardiography
echography
genetics
heterozygote
hypertrophic cardiomyopathy
middle aged
mutation
pathology
pathophysiology
physiology
prognosis
systole
Adult
Cardiomyopathy, Hypertrophic
Echocardiography
Female
Heterozygote
Humans
Male
Middle Aged
Mutation
Myocardium
Phenotype
Prognosis
Reproducibility of Results
Systole
Issue Date: 2012
Citation: Yiu K.H., Atsma D.E., Delgado V., Ng A.C.T., Witkowski T.G., Ewe S.H., Auger D., Holman E.R., van Mil A.M., Breuning M.H., Tse H.F., Bax J.J., Schalij M.J., Marsan N.A. (2012). Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers. PLoS ONE 7 (5) : e36115. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0036115
Rights: Attribution 4.0 International
Abstract: Background: To evaluate the presence of myocardial structural alterations and subtle myocardial dysfunction during familial screening in asymptomatic mutation carriers without hypertrophic cardiomyopathy (HCM) phenotype. Methods and Findings: Sixteen HCM families with pathogenic mutation were studied and 46 patients with phenotype expression (Mut+/Phen+) and 47 patients without phenotype expression (Mut+/Phen-) were observed. Twenty-five control subjects, matched with the Mut+/Phen- group, were recruited for comparison. Echocardiography was performed to evaluate conventional parameters, myocardial structural alteration by calibrated integrated backscatter (cIBS) and global and segmental longitudinal strain by speckle tracking analysis. All 3 groups had similar left ventricular dimensions and ejection fraction. Basal anteroseptal cIBS was the highest in Mut+/Phen+ patients (-14.0±4.6 dB, p<0.01) and was higher in Mut+/Phen- patients as compared to controls (-17.0±2.3 vs. -22.6±2.9 dB, p<0.01) suggesting significant myocardial structural alterations. Global and basal anteroseptal longitudinal strains (-8.4±4.0%, p<0.01) were the most impaired in Mut+/Phen+ patients as compared to the other 2 groups. Although global longitudinal strain was similar between Mut+/Phen- group and controls, basal anteroseptal strain was lower in Mut+/Phen- patients (-14.1±3.8%, p<0.01) as compared to controls (-19.9±2.9%, p<0.01), suggesting a subclinical segmental systolic dysfunction. A combination of >-19.0 dB basal anteroseptal cIBS or >-18.0% basal anteroseptal longitudinal strain had a sensitivity of 98% and a specificity of 72% in differentiating Mut+/Phen- group from controls. Conclusion: The use of cIBS and segmental longitudinal strain can differentiate HCM Mut+/Phen- patients from controls with important clinical implications for the family screening and follow-up of these patients. © 2012 Yiu et al.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/161984
ISSN: 19326203
DOI: 10.1371/journal.pone.0036115
Rights: Attribution 4.0 International
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