Preclinical Systolic and Diastolic Dysfunction Assessed by Tissue Doppler Imaging is Associated With Elevated Plasma Pro-B-type Natriuretic Peptide Concentrations
Abstract
Background
Heart failure is a major public health problem. To improve its grave prognosis, early identification of cardiac dysfunction is mandatory. Conventional echocardiography is not suitable for this. Tissue Doppler imaging (TDI), however, could be so.
Methods and Results
Within a large community-based population-study (n = 1012), cardiac function was evaluated by conventional echocardiography (left ventricular hypertrophy, dilatation, systolic, and severe diastolic dysfunction), TDI, and plasma proBNP. Averages of peak systolic (s′), early diastolic (e′), and late diastolic (a′) velocities from 6 mitral annular sites were used. TDI was furthermore quantified by a combined index (eas-index) of diastolic and systolic performance: e′/(a′ × s′). Compared with controls, persons with elevated plasma proBNP concentrations (n = 100) displayed lower systolic and diastolic performance by TDI, in terms of lower s′ (P = 0.017) and a′ (P < .001), and higher e′/a′ (P = .002) and eas-index (P < .001). This pattern remained significant after multivariable adjustment for age, sex, body mass index, heart rate, estimated glomerular filtration rate, hypertension, diabetes, ischemic heart disease, and conventional echocardiography. Furthermore, TDI provided incremental information over conventional echocardiography in predicting elevated plasma proBNP concentrations.
Conclusions
Preclinical systolic and diastolic dysfunction by TDI is associated with elevated plasma proBNP levels, even when conventional echocardiography is normal.
Key Words: Heart failure, population, diagnosis, echocardiography, ProBNP
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Supported by grants from the Lundbeck Foundation, the Novo Nordisk Foundation, the Copenhagen County Research Foundation, the C.C. Klestrup Foundation, the Foundation Promoting Medicine, the Lykfeldt Foundation, the CM Sorensen and Wife's Foundation, and The Danish Heart Foundation (07-10-R60-A1698-B132-22413), Copenhagen, Denmark. Peter Sogaard has received honoraria from GE Healthcare. The sponsors had no role in the study design, data collection, data analysis, data interpretation nor in the writing of the manuscript.
PII: S1071-9164(09)00020-7
doi:10.1016/j.cardfail.2009.01.005
© 2009 Elsevier Inc. All rights reserved.
