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Relationship between proximal aortic stiffness assessed with CMR and left ventricular diastolic function in a bicentric asymptomatic population with preserved left ventricular ejection fraction
© Redheuil et al; licensee BioMed Central Ltd. 2011
Published: 2 February 2011
To evaluate the direct relation between proximal aortic function and left ventricular diastolic function in individuals with normal LVEF free of overt cardiovascular disease.
Left ventricular (LV) diastolic dysfunction is considered to be an important determinant of heart failure with preserved LV ejection fraction (LVEF). Hypertension, diabetes and aging leading to increased aortic stiffness have been related to impaired diastolic function. Novel CMR measures of proximal aortic function have been recently shown to be better markers of vascular aging than conventional measures of arterial stiffness but their relationship to LV diastolic function has not been reported.
We studied 144 subjects (70 men, 74 women, age 44±16 [13-79] years) from 2 academic centers (Baltimore, USA; Paris, France). Ascending aortic strain was determined by CMR using an automated segmentation of SSFP cine acquisitions. Aortic arch pulse wave velocity (PWV) was measured by CMR from phase-contrast sequence for flow-wave analysis and multiple T1 spin echo images for aortic length measurement. Conventional LV diastolic function indices were measured by echo-Doppler (E/A, e’, E/e’); carotid pressures and carotid-femoral PWV (cfPWV) were measured using applanation tonometry. Central pressures were used to calculate aortic distensibility and carotid augmentation index (AIx).
Proximal aortic function measured by CMR is strongly associated with subclinical impairment in diastolic left ventricular function in subjects with preserved LVEF independent of the effects of age, gender, BMI, mean central pressure and LV mass. These novel markers of proximal aortic stiffness estimated by CMR have a stronger correlation with LV diastolic function than conventional markers of arterial stiffness.
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.