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Updated: Jul 15, 2026

Pulse Wave Velocity Testing in the Baltimore Longitudinal Study of Aging
Published on: February 7, 2014
Pulse wave velocity is inversely related to vertebral bone density in hemodialysis patients
Paolo Raggi1, Antonio Bellasi, Emiliana Ferramosca
1Division of Cardiology and Department of Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA. praggi@emory.edu
Insights
Low spine bone mineral density (BMD) is linked to increased pulse wave velocity (PWV) in chronic kidney disease patients. Quantitative computed tomography (QCT) is recommended over dual-energy x-ray absorptiometry for assessing spine BMD in dialysis patients.
Area of Science:
- Nephrology
- Cardiology
- Radiology
Background:
- Chronic kidney disease (CKD) stage 5 is associated with bone mineral metabolism abnormalities.
- These abnormalities may contribute to cardiovascular disease (CVD) incidence.
- Noninvasive imaging can predict concurrent bone and vascular disease.
Purpose of the Study:
- To investigate the relationship between bone mineral density (BMD) and pulse wave velocity (PWV).
- To compare dual-energy x-ray absorptiometry (DXA) and quantitative computed tomography (QCT) for spine BMD assessment in dialysis patients.
Main Methods:
- 110 maintenance hemodialysis patients underwent measurements of PWV and spine BMD/T-scores using DXA and QCT.
- Associations between BMD, T-scores, and PWV were analyzed.
- Correlation with aorta and coronary calcification was assessed.
Main Results:
- Lower QCT-assessed T-scores correlated with older age, white race, diabetes, lower diastolic blood pressure, and lower albumin.
- Increased PWV was significantly associated with decreased QCT-assessed BMD (P<0.001).
- No relationship was found between DXA-assessed BMD and PWV; QCT T-scores weakly correlated with aorta calcification.
Conclusions:
- Low spine BMD, assessed by QCT, is associated with increased PWV in stage 5 CKD patients.
- This supports a link between vascular and bone disease in this population.
- QCT is superior to DXA for assessing spine BMD in dialysis patients.
Abstract:
Abnormalities of bone mineral metabolism in patients with stage-5 chronic kidney disease may contribute to the high incidence of cardiovascular disease. Noninvasive imaging methods may help predict the simultaneous presence of vasculopathy and bone disease. Accordingly, we measured pulse wave velocity and bone mineral density (BMD), and T-scores (number of SDs below the BMD of a younger reference group) of the spine by both dual energy x-ray absorptiometry and quantitative computed tomography (QCT) in 110 maintenance hemodialysis patients. Older age, white race, diabetes mellitus, lower diastolic blood pressure, and lower albumin levels were associated with lower QCT-assessed T-scores (each P<0.05). After age and multivariable adjustment, pulse wave velocity (PWV) increased as QCT BMD decreased (the prevalence of PWV >or=9 m/s was 32.4%, 61.8%, and 76.5% for participants in the highest to the lowest tertile of QCT-assessed BMD; P<0.001). In contrast, there was no relationship between spine dual energy x-ray absorptiometry-BMD and PWV. In unadjusted models, thoracic spine QCT-assessed T-scores correlated significantly, albeit weakly, with aorta calcification (r=0.22; P=0.01) but not with coronary calcification. The odds ratio of PWV >or=9 m/s for patients taking vitamin D(3) or its analogs was 0.51 (95% CI: 0.19 to 1.39). In conclusion, low spine BMD is associated with increased PWV in stage-5 chronic kidney disease, supporting the notion of a close interaction of vascular and bone disease in this patient group. QCT and not dual energy x-ray absorptiometry should be used to assess spine BMD in dialysis patients.
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