The bone-vascular axis in chronic kidney disease
- PMID: 20508522
- PMCID: PMC3001327
- DOI: 10.1097/MNH.0b013e32833a3d67
The bone-vascular axis in chronic kidney disease
Abstract
Purpose: This review highlights the most recent publications addressing the relationship between bone and vascular calcification in patients with chronic and end-stage kidney disease.
Recent findings: The relatively new term 'chronic kidney disease-mineral bone disorder' reflects the growing reach of chronic kidney disease research into the realm of systems physiology, involving a triad of renal, skeletal, and vascular tissues. Recent studies address underlying mechanisms of the bone and vascular complications of chronic kidney disease and point to a variety of biochemical factors, including phosphatonins (fibroblast growth factor-23, matrix extracellular phosphoglycoprotein), bone morphogenetic protein 7, osteoprotegerin, matrix GLA protein, ectonucleotide pyrophosphatase/phosphodiesterase 1, alkaline phosphatase, and lipid oxidation products. Studies also demonstrate that agents used for treatment of one component of the triad often act on the other components of the triad - beneficially or adversely. These findings emphasize the importance of avoiding the subspecialty, single organ viewpoint when treating individual components of chronic kidney disease-mineral bone disorder.
Summary: The consistent synchrony among chronic kidney disease, aortic calcification, and bone loss offers clues to underlying mechanisms for the systemic abnormalities.
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Tomiyama C, Carvalho AB, Higa A, et al. Coronary Calcification is Associated with Lower Bone Formation Rate in CKD Patients Not Yet in Dialysis Treatment. J Bone Miner Res. 2009 This report address the controversy of whether the association between bone density and vascular calcification is merely a result of both processes being age-related.
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- Towler DA. Vascular calcification in ESRD: Another cloud appears in the perfect storm--but highlights a silver lining? Kidney Int. 2004;66:2467–8. - PubMed
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