Chasing the reflected wave back into the heart: a new hypothesis while the jury is still out

Abstract

Background:

Arterial stiffness directly influences cardiac function and is independently associated with cardiovascular risk. However, the influence of the aortic reflected pulse pressure wave on left ventricular function has not been well characterized. The aim of this study was to obtain detailed information on regional ventricular wall motion patterns corresponding to the propagation of the reflected aortic wave on ventricular segments.

Methods:

Left ventricular wall motion was investigated in a group of healthy volunteers (n = 14, age 23 ± 3 years), using cardiac magnetic resonance navigator-gated tissue phase mapping. The left ventricle was divided into 16 segments and regional wall motion was studied in high temporal detail.

Results:

Corresponding to the expected timing of the reflected aortic wave reaching the left ventricle, a characteristic “notch” of regional myocardial motion was seen in all radial, circumferential, and longitudinal velocity graphs. This notch was particularly prominent in septal segments adjacent to the left ventricular outflow tract on radial velocity graphs and in anterior and posterior left ventricular segments on circumferential velocity graphs. Similarly, longitudinal velocity graphs demonstrated a brief deceleration in the upward recoil motion of the entire ventricle at the beginning of diastole.

Conclusion:

These results provide new insights into the possible influence of the reflected aortic waves on ventricular segments. Although the association with the reflected wave appears to us to be unambiguous, it represents a novel research concept, and further studies enabling the actual recording of the pulse wave are required.

Keywords:

• arterial pressure wave
• reflected wave
• ventricular wall motion
• cardiovascular magnetic resonance imaging
• tissue phase mapping

Acknowledgements

This research was funded by the British Heart Foundation, and was supported by the Oxford Partnership Comprehensive Biomedical Research Centre, with funding from the Department of Health’s National Institute for Health Research Biomedical Research Centre.

Disclosure

The authors report no conflicts of interest in this work.