TY - JOUR
T1 - The Diastolic Function to Cyclic Variation of Myocardial Ultrasonic Backscatter Relation
T2 - The Influence of Parametrized Diastolic Filling (PDF) Formalism Determined Chamber Properties
AU - Lloyd, Christopher W.
AU - Shmuylovich, Leonid
AU - Holland, Mark R.
AU - Miller, James G.
AU - Kovács, Sándor J.
N1 - Funding Information:
The authors would also like to thank the staff of the Cardiac Procedure Center at Washington University Medical Center’s Barnes-Jewish Hospital for their assistance and sonographer, Peggy Brown, for her expert acquisition of the ultrasonic data. This work was supported, in part, by NIH HL040302 and NSF CBET 0717830 , the Alan A. and Edith L Wolff Charitable Trust and the Barnes-Jewish Hospital Foundation . Leonid Shmuylovich is a recipient of an American Heart Association Pre-doctoral fellowship.
PY - 2011/8
Y1 - 2011/8
N2 - Myocardial tissue characterization represents an extension of currently available echocardiographic imaging. The systematic variation of backscattered energy during the cardiac cycle (the " cyclic variation" of backscatter) has been employed to characterize cardiac function in a wide range of investigations. However, the mechanisms responsible for observed cyclic variation remain incompletely understood. As a step toward determining the features of cardiac structure and function that are responsible for the observed cyclic variation, the present study makes use of a kinematic approach of diastolic function quantitation to identify diastolic function determinants that influence the magnitude and timing of cyclic variation. Echocardiographic measurements of 32 subjects provided data for determination of the cyclic variation of backscatter to diastolic function relation characterized in terms of E-wave determined, kinematic model-based parameters of chamber stiffness, viscosity/relaxation and load. The normalized time delay of cyclic variation appears to be related to the relative viscoelasticity of the chamber and predictive of the kinematic filling dynamics as determined using the parametrized diastolic filling formalism (with r-values ranging from .44 to .59). The magnitude of cyclic variation does not appear to be strongly related to the kinematic parameters.
AB - Myocardial tissue characterization represents an extension of currently available echocardiographic imaging. The systematic variation of backscattered energy during the cardiac cycle (the " cyclic variation" of backscatter) has been employed to characterize cardiac function in a wide range of investigations. However, the mechanisms responsible for observed cyclic variation remain incompletely understood. As a step toward determining the features of cardiac structure and function that are responsible for the observed cyclic variation, the present study makes use of a kinematic approach of diastolic function quantitation to identify diastolic function determinants that influence the magnitude and timing of cyclic variation. Echocardiographic measurements of 32 subjects provided data for determination of the cyclic variation of backscatter to diastolic function relation characterized in terms of E-wave determined, kinematic model-based parameters of chamber stiffness, viscosity/relaxation and load. The normalized time delay of cyclic variation appears to be related to the relative viscoelasticity of the chamber and predictive of the kinematic filling dynamics as determined using the parametrized diastolic filling formalism (with r-values ranging from .44 to .59). The magnitude of cyclic variation does not appear to be strongly related to the kinematic parameters.
KW - Cyclic variation
KW - Myocardial ultrasound
KW - Parametrized diastolic filling formalism
KW - Tissue characterization
UR - http://www.scopus.com/inward/record.url?scp=79959847211&partnerID=8YFLogxK
U2 - 10.1016/j.ultrasmedbio.2011.05.002
DO - 10.1016/j.ultrasmedbio.2011.05.002
M3 - Article
C2 - 21683506
AN - SCOPUS:79959847211
SN - 0301-5629
VL - 37
SP - 1185
EP - 1195
JO - Ultrasound in Medicine and Biology
JF - Ultrasound in Medicine and Biology
IS - 8
ER -