Longitudinally and circumferentially directed movements of the left ventricle studied by cardiovascular magnetic resonance phase contrast velocity mapping
© Codreanu et al; licensee BioMed Central Ltd. 2010
Received: 7 February 2010
Accepted: 17 August 2010
Published: 17 August 2010
Using high resolution cardiovascular magnetic resonance (CMR), we aimed to detect new details of left ventricular (LV) systolic and diastolic function, to explain the twisting and longitudinal movements of the left ventricle.
Using CMR phase contrast velocity mapping (also called Tissue Phase Mapping) regional wall motion patterns and longitudinally and circumferentially directed movements of the left ventricle were studied using a high temporal resolution technique in healthy male subjects (n = 14, age 23 ± 3 years).
Previously undescribed systolic and diastolic motion patterns were obtained for left ventricular segments (based on the AHA segmental) and for basal, mid and apical segments. The summation of segmental motion results in a complex pattern of ventricular twisting and longitudinal motion in the normal human heart which underlies systolic and diastolic function. As viewed from the apex, the entire LV initially rotates in a counter-clockwise direction at the beginning of ventricular systole, followed by opposing clockwise rotation of the base and counter-clockwise rotation at the apex, resulting in ventricular torsion. Simultaneously, as the entire LV moves in an apical direction during systole, the base and apex move towards each other, with little net apical displacement. The reverse of these motion patterns occur in diastole.
Left ventricular function may be a consequence of the relative orientations and moments of torque of the sub-epicardial relative to the sub-endocardial myocyte layers, with influence from tethering of the heart to adjacent structures and the directional forces associated with blood flow. Understanding the complex mechanics of the left ventricle is vital to enable these techniques to be used for the evaluation of cardiac pathology.
Left ventricular (LV) function is geometrically and mechanically complex. Advances in cardiac imaging techniques have accompanied ongoing efforts to define the mechanisms of three dimensional ventricular motion [1–7]. Current theories explaining LV motion are controversial. The "myocardial band model" divides the myocardium into two distinct helicoids [6, 7], but fails to explain the mechanisms of myocardial contraction after repolarization and ventricular motion in diastole. Additionally, the embryological development of the heart, and the failure of anatomists to separate "bands" on anatomical dissection, have further challenged this theory [8–12].
Cardiovascular magnetic resonance (CMR) has allowed detailed evaluation of LV wall motion throughout the cardiac cycle, using myocardial velocity encoding techniques [13, 14]. Here, we have used results from CMR phase contrast velocity mapping with high temporal resolution, to characterise longitudinal and rotational movements of the left ventricle in healthy human subjects.
CMR scans were performed on fourteen healthy male volunteers (age 23 ± 3 years). All subjects were non-smokers, with no history of cardiovascular disease. The study was conducted according to the principles of the Declaration of Helsinki and was approved by a local Oxfordshire Clinical Research Ethics Committee. Each subject provided written informed consent.
CMR scans were performed using a 1.5 Tesla Siemens Sonata clinical scanner. Pilot images, followed by horizontal and vertical long axis cine images were acquired using an SSFP pulse sequence. Cine images for navigator gated high temporal resolution phase contrast velocity mapping were acquired using a black blood segmented k-space spoiled gradient echo sequence (TR = 13.8 ms, TE = 5.0 ms, flip angle = 15°, bandwidth = 650 Hz/pixel, FOV = 400 × 300 mm, matrix = 256 × 96) [13, 14].
To obtain velocity measurements, three equidistant short-axis slices along the left ventricle were evaluated using 3-directionally encoded, time resolved phase contrast velocity maps. Velocity encoding was performed by including a phase image with no velocity encoding followed by images with a bipolar gradient in read, phase or slice direction after each RF pulse to the otherwise identical sequence (venc in-plane = 20 cm/s, venc through-plane = 30 cm/s). Acquisition was prospectively gated, typically covering between 80 to 90% of the cardiac cycle, meaning the contribution of atrial contraction on left ventricular motion was not possible to assess. Post-processing was performed in the standard fashion of subtracting the phase from the image with no velocity encoding, followed by conversion of the phase data into velocity maps.
The basal slice was positioned parallel to the base of the heart, distal to the LV outflow tract. Basal, midventricular and apical slices were positioned 15 to 20 mm apart, depending on the heart size. With cardiac and respiratory gating, each short axis acquisition took approximately 3-5 minutes, with an average of 60-70 phases per cardiac cycle. Cardiac phases were determined, with the end systole defined as the smallest LV cavity.
Analysis was performed using customized software (Matlab, version 6.5; Mathworks, Natick, Mass), where the left ventricle was divided into 16 segments (six basal, six middle and four apical) according to the American Heart Association model . Ventricular velocities and regional wall motion patterns were determined for all individual segments. The myocardial velocity results, or time varying vectors derived from all 3 directional components of velocity, have been subdivided into "longitudinal" and "circumferential" components (from one through-plane component, and two in-plane velocity datasets, respectively). All myocardial velocities are expressed as cm/s. Circumferential velocities are described as clockwise or counter-clockwise, as viewed from the ventricular apex.
These results demonstrate regional variations in circumferential and longitudinal motion within the left ventricular during systole and diastole. We believe this complex pattern of LV segmental motion, demonstrated using cardiac phase contrast velocity mapping, can be largely explained by the anatomical orientation of cardiomyocytes within the left ventricle and their attachments to adjacent structures.
On the anterior aspect of the heart, a significant part of the outer-surface aggregates cross the interventricular sulcus, extending to the right ventricle, great vessels and fibrous structures. These aggregates (labelled as type 1 in Figure 6) have been described on manual dissection and recently using diffusion tensor magnetic resonance imaging [17, 18]. Having the longest extension onto the anterior heart surface, they are likely to determine the dominant direction of initial LV rotation, causing the entire ventricle to rotate in a counter-clockwise direction, as viewed from the apex. We believe this explains the initial counter-clockwise movement of the left ventricle at the beginning of systole (Figure 1, wave a). Similarly, contraction of myocardial aggregates limited to the left ventricle (labelled as type 2 in Figure 6B and 6C) would result in LV torsion, i.e. in a clockwise rotation of the ventricular base (Figure 1, wave c) and a counter-clockwise motion of the apex, as observed in the velocity graphs. Since these aggregates are shorter, net motion only becomes apparent after the initial counter-clockwise rotation of the entire left ventricle, which is dominated by the longer (type 1) aggregates. The contraction of both type 1 and type 2 aggregates together may therefore explain the displacement of the ventricular apex anteriorly (Figure 6) and explain why the apex beat can be palpated on the anterior chest wall.
On the posterior aspect of the left ventricle, some of the outer surface aggregates also cross the interventricular sulcus, extending to the posterior surface of the right ventricle (labeled as type 3 in Figure 6C) [17, 18]. The contraction of these aggregates may contribute to the clockwise rotation of the ventricular base during LV ejection, provided they end within the LV wall. Additionally, any of these aggregates extending to various support structures outside the left ventricle (great vessels, valvular rings and fibrous structures) may produce a biventricular counter-clockwise rotation during systole. Thus, contraction of outer surface aggregates, which extend to the anterior heart surface (type 1), may explain the initial counter-clockwise rotation of the entire left ventricle (Figure 1, wave a), whilst the simultaneous contraction of the outer surface aggregates limited to the left ventricle (type 2), explains the clockwise rotation of the LV base and the counter-clockwise movement of the apex (Figure 1, basal segments 1-6 vs. apical segments 13-16).
A key consideration for ventricular motion may be which parts of the heart (predominantly basal) are tethered in the mediastinum and thorax by large vascular and pericardial attachments, and which (more apical) are free to rotate. This is evident at the beginning of ventricular repolarization where there is a sudden change in movement direction occurring only at the apex (Figure 1, wave e in apical segments 13-16), where the net result for basal segments is a counter-clockwise rotation, superimposed on a brief clockwise rotation of the entire LV. A further consideration is the phasic, directional forces (and hence possible displacements) associated with the momentum changes of blood, particularly into the outflow tracts and great arteries in early systole. Slight torque may be associated with acceleration (and later deceleration) of blood into the helical curvatures of the great arteries, though this relationship is likely to be complex, so requires further evaluation.
Longitudinal motion of the LV during systole may be explained by contraction of the predominantly longitudinally oriented epi- and endocardial, trabecular and papillary myocytes. Repolarization leads to cessation of active myocardial contraction, although minimal blood flow still occurs at the end of reduced ejection due to the kinetic energy of the ejected blood . There are two simultaneously occurring, and partly opposing components which likely contribute to longitudinal relaxation. Firstly, after repolarization, the LV base and apex move away from each other due to passive ventricular untwisting, resulting in an upward displacement of the base and a downward movement of the apex. Secondly, the potential importance of momentum changes, which are complex between atria, ventricles, outflow tracts and aortic arch should be considered. The results for basal motion would be consistent with elastic recoil, from these structures, pulling the ventricle back to its initial location after repolarization. The peak velocities of this upward longitudinal motion in diastole exceeding all other cardiac velocities during a cardiac cycle, strongly supports this "recoil" hypothesis.
Ventricular filling is likely to have multiple contributing factors. Firstly, a passive component, where repolarization leads to cessation of myocardial contraction and to ventricular wall relaxation, allowing blood to be expelled from the atria. Whether a suction component results from ventricular untwisting remains controversial [20, 22]. We also believe there could be a mechanical, or recoil component, where the left ventricle is being pulled towards its initial location by the adjacent great vessels and mediastinum. This would lead to fast recoil motion against the filled left atrium and substantially increase the pressure difference across the mitral valve, contributing to ventricular filling.
The complex pattern of LV motion can be explained by the helical orientation of cardiomyocytes in the healthy heart. From these results we believe that left ventricular torsion is mainly a consequence of the relative orientations and moments of torque of the sub-epicardial relative to the sub-endocardial myocyte layers, with influence from tethering of the heart to the mediastinum and great vessels and the directional forces associated with blood flow. Whether assessment of these detailed systolic and diastolic parameters would assist in the early diagnosis of cardiac disease requires further evaluation.
This research was funded by the British Heart Foundation and by the Oxford Partnership Comprehensive Biomedical Research Centre with funding from the Department of Health's NIHR Biomedical Research Centres funding scheme.
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