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Published on: June 2, 2022
Bone mineral density, vascular calcifications, and arterial stiffness in peritoneal dialysis patients
Teresa Adragao1, Patrícia Branco, Rita Birne
1Nephrology Department, Santa Cruz Hospital, Lisbon, Portugal. tadragao@netcabo.pt
Insights
Lower bone mineral density (BMD) in the femoral neck, not the lumbar spine, correlates with increased arterial stiffness, vascular calcifications, and peripheral artery disease in peritoneal dialysis patients, suggesting a bone-cardiovascular link.
Area of Science:
- Nephrology
- Cardiology
- Endocrinology
Background:
- Bone disease and cardiovascular disease are common comorbidities in patients undergoing dialysis.
- The relationship between bone mineral density (BMD) and vascular complications in this population requires further elucidation.
Purpose of the Study:
- To investigate the association between BMD, evaluated by dual-energy X-ray absorptiometry (DXA), and markers of vascular disease in patients on peritoneal dialysis.
Main Methods:
- Bone mineral density (BMD) was assessed using DXA.
- Vascular calcifications were quantified using a vascular calcification score from plain X-rays.
- Arterial stiffness was measured by pulse wave velocity (PWV) using the Complior device.
Main Results:
- Lower BMD at the femoral neck, but not the lumbar spine, was significantly correlated with higher PWV (p = 0.037).
- Reduced femoral neck BMD was also associated with a higher vascular calcification score (p = 0.013) and the presence of peripheral artery disease (p = 0.006).
Conclusions:
- These findings support a connection between bone health and cardiovascular disease in patients on peritoneal dialysis.
- Femoral neck BMD appears to be a more relevant indicator than lumbar spine BMD for vascular complications in this cohort.
Abstract:
The objective of this study was to evaluate the correlation of bone mineral density (BMD), evaluated by DXA, with vascular calcifications, arterial stiffness, and vascular disease in patients on peritoneal dialysis. Vascular calcifications were evaluated by vascular calcification score on plain x ray, and arterial stiffness was measured by pulse wave velocity using the Complior device (Artech Medical, Pantin, France). Adjusting for multiple factors, lower BMD at the femoral neck, but not at the lumbar spine, was associated with higher pulse wave velocity (p = 0.037), higher vascular calcification score (p = 0.013), and peripheral artery disease (p = 0.006). These data reinforce the hypothesis of the existence of a link between bone disease and cardiovascular disease in dialysis patients.
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