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Updated: Jun 18, 2025

Measuring the Carotid to Femoral Pulse Wave Velocity Cf-PWV to Evaluate Arterial Stiffness
Published on: May 3, 2018
Association of Carotid-Femoral Pulse Wave Velocity and Ejection Duration with Target Organ Damage
Yaya Bai1, Huiying Jia2, Alberto Avolio3
1Department of Geriatrics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, 200025 Shanghai, China.
Insights
Carotid-femoral pulse wave velocity (cfPWV) is linked to kidney damage, while ejection duration (ED) relates to heart issues. Together, cfPWV and ED influence left ventricular hypertrophy (LVH).
Area of Science:
- Cardiovascular Physiology
- Renal Medicine
- Biomarkers of Organ Damage
Background:
- Carotid-femoral pulse wave velocity (cfPWV) and ejection duration (ED) are distinct hemodynamic parameters.
- These parameters have differential impacts on target organ damage (TOD).
Purpose of the Study:
- To investigate the relationship between cfPWV, ED, and TOD.
- To determine how cfPWV and ED individually and collectively influence organ damage markers.
Main Methods:
- A cohort of 1254 patients was analyzed.
- cfPWV was measured, and ED was calculated using SphygmoCor software.
- TOD markers included left ventricular hypertrophy (LVH), microalbuminuria, chronic kidney disease (CKD), and carotid intima-media thickness (CIMT).
Main Results:
- cfPWV correlated positively with left ventricular mass index (LVMI) and albumin-creatinine ratio (ACR).
- ED correlated negatively with LVMI and positively with estimated glomerular filtration rate (eGFR).
- cfPWV was associated with CKD, while ED was associated with LVH. High cfPWV and low ED were linked to elevated LVH.
Conclusions:
- cfPWV shows a stronger association with renal damage, whereas ED is more closely linked to cardiac dysfunction.
- cfPWV and ED interact and jointly affect LVH.
- Understanding these relationships can inform strategies for managing TOD.
Background:
Carotid-femoral pulse wave velocity (cfPWV) and ejection duration (ED) have different impacts on target organ damage (TOD). The aim of this study was to determine the relationship of cfPWV and ED with TOD.
Methods:
A total of 1254 patients (64.27% males) from Ruijin Hospital were enrolled in this study from December 2018 to August 2022. Medical records, blood samples and urine samples were collected. The cfPWV was measured and ED was generated using SphygmoCor software (version 8.0, AtCor Medical, Sydney, Australia). TOD including left ventricular hypertrophy (LVH), microalbuminuria, chronic kidney disease (CKD), and abnormality of carotid intima-media thickness (CIMT) were evaluated.
Results:
Multiple stepwise linear regression models of cfPWV and ED (individually or together) showed that cfPWV was positively correlated with left ventricular mass index (LVMI) ( = 0.131, p = 0.002) and Log (albumin-creatinine ratio, ACR) ( = 0.123, p = 0.004), while ED was negatively correlated with LVMI ( = -0.244, p 0.001) and positively correlated with the estimated glomerular filtration rate (eGFR) ( = 0.115, p = 0.003). When cfPWV and ED were added separately or together in multiple stepwise logistic regression models, cfPWV was associated with CKD [odds ratio (OR) = 1.240, 95% confidence interval (CI) 1.055-1.458, p = 0.009], while ED was associated with LVH (OR = 0.983, 95% CI 0.975-0.992, p 0.001). In the control group with normal cfPWV and normal ED, LVH was significantly lower in patients with high ED (OR = 0.574, 95% CI 0.374-0.882, p = 0.011), but significantly elevated in those with high cfPWV and low ED (OR = 6.799, 95% CI 1.305-35.427, p = 0.023).
Conclusions:
cfPWV was more strongly associated with renal damage, while ED was more strongly associated with cardiac dysfunction. cfPWV and ED affect each other, and together have an effect on LVH.
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