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Updated: May 15, 2025

Measuring the Carotid to Femoral Pulse Wave Velocity Cf-PWV to Evaluate Arterial Stiffness
Published on: May 3, 2018
Heart-carotid pulse-wave velocity via laser-Doppler vibrometry as a biomarker for arterial stiffening: a feasibility
Simeon Beeckman1, Smriti Badhwar2, Yanlu Li3
1Simeon Beeckman and Patrick Segers are with IBiTech-BioMMedA, Ghent University, Ghent, Belgium.
Insights
Laser Doppler vibrometry (LDV) shows promise for measuring heart-carotid pulse-transit time (hcPTT), a new biomarker for arterial stiffness. This method includes the ascending aorta, offering a more comprehensive assessment of cardiovascular risk.
Area of Science:
- Cardiovascular research
- Biomedical engineering
- Medical diagnostics
Background:
- Large artery stiffening increases cardiovascular risk and organ damage.
- Pulse-wave velocity (PWV) is a key biomarker for arterial stiffness.
- Previous work established laser Doppler vibrometry (LDV) for carotid-femoral PWV (cfPWV) measurement.
Purpose of the Study:
- To assess the feasibility of using an LDV prototype to measure heart-carotid pulse-transit time (hcPTT).
- To establish hcPTT as a precursor to heart-carotid PWV (hcPWV) measurement.
- To evaluate hcPTT's potential to include the ascending aorta in arterial stiffness assessment.
Main Methods:
- Simultaneous signal acquisition from the chest and carotid artery in 100 patients.
- Utilizing fiducial points: second heart sound (S2) from the heart signal and foot/dicrotic notch (DN) from the carotid waveform.
- Evaluating four distinct hcPTT estimations based on two heart signal sites.
Main Results:
- hcPTT estimations showed convincing correlations with established arterial stiffness determinants like age (ρ=0.377).
- Combining S2 from the heart base with carotid DN yielded the most significant correlations.
- The LDV method demonstrated feasibility for hcPTT inference in approximately 94% of measurements.
Conclusions:
- LDV is a feasible tool for inferring hcPTT, a potential new biomarker for arterial stiffness.
- This method offers a non-invasive approach to assess arterial stiffness, including the ascending aorta.
- LDV-derived hcPTT may serve as a valuable corollary biomarker for early cardiovascular risk detection.
Abstract:
Objective. Large artery stiffening leads to an increase in cardiovascular risk and organ damage of the kidneys, brain or the heart. Biomarkers that allow for early detection of this phenomenon are a point of interest in research, with pulse-wave velocity (PWV) having been proven useful in predicting and monitoring arterial stiffness. We previously introduced a laser Doppler vibrometry (LDV) prototype which can measure carotid-femoral PWV (cfPWV). In this work, we assess the feasibility of using the same device to infer heart-carotid pulse-transit time (hcPTT) as a first step towards measuring heart-carotid PWV (hcPWV). The advantage of hcPWV over cfPWV is that the ascending aorta, which is the most distensible segment of the aorta contributing most to total arterial compliance, is included in the arterial pathway.Approach. Signals were simultaneously acquired from a location on the chest (near either the base or the apex of the heart) and the right carotid artery for 100 patients (45% female). Fiducial points on the heart waveforms are associated with opening and closure (second heart sound; S2) of the aortic valve, which can be combined with, respectively, the foot and dicrotic notch (DN) of the carotid waveform to retrieve hcPTT. Considering two distinct heart-signal measurement sites, four hcPTT estimations are evaluated in about 94% of all measurements.Main results. Correlations between these and known predictors of arterial stiffness i.e. age, blood pressure and carotid-femoral PTT via applanation tonometry indicated that combining S2 from a heart-measurement site located at the base of the heart, with the carotid DN yields hcPTT providing convincing correlations with known determinants of arterial stiffness (ρ = 0.377 with age).Significance.We conclude that LDV may provide a corollary biomarker of arterial stiffness, encompassing the ascending aorta.
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