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The 3d left ventricular geometry integrated in myocardial wall stress estimation is more sensitive than end diastolic mass/volume ratio to characterize afterload-related left ventricular remodeling
© Kachenoura et al; licensee BioMed Central Ltd. 2011
- Published: 2 February 2011
- Left Ventricular Mass
- Left Ventricular Remodel
- Aortic Valve Stenosis
- Left Ventricular Geometry
- Concentric Remodel
To analyze left ventricular (LV) remodeling using an accurate 3D evaluation of afterload-related changes in LV geometry.
To maintain an effective LV-arterial coupling the LV adapts to the increased afterload caused by aging or cardiovascular disease. However, subsequent changes in LV mass and concentric remodeling have been associated with poor outcome. To understand LV remodeling, we studied variations of 3D myocardial wall stress (MWS), its geometrical factor as well as diastolic LV mass to volume ratio (LVM/EDV) on a population with a wide range of afterload.
Indeed, we studied 57 patients divided into three subgroups: 1) C1 included 22 healthy subjects aged between 22 and 37 years (26±5 years), (2) C2 included 23 healthy subjects aged between 41 et 81 years (55±9 years) and 3) AVS included 12 subjects (75±14 years) with aortic valve stenosis (AVS) characterized by (valve area=0.78±0.19 cm2). All subjects had short axis cine CMR acquisitions (GE 1.5T) followed by carotid applanation tonometry calibrated using brachial pressures recorded during CMR. After myocardial delineation, the LV geometrical factor LVGF, previously described by Grossman, was calculated as a combination of the local LV radius and myocardial thickness while considering the LV longitudinal curvature to correct for partial volume effects, especially in apical slices. This LVGF was combined with peak systolic pressures (PSP) resulting in MWS. For AVS patients, the echocardiographic transaortic valve maximal gradient was added to the tonometric PSP.
The described 3D evaluation of LV geometry, which can be easily integrated to standard CMR LV function evaluation since it only requires routine myocardial delineation in systole, sensitively characterized LV remodeling related to aging or to AVS.
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.