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Calcific uraemic arteriolopathy: an update
Natasha M Rogers1, Patrick Toby H Coates
1Transplantation Immunology Laboratory and Department of Medicine, University of Adelaide, The Queen Elizabeth Hospital (TQEH) Campus, Woodville, Australia.
Insights
Calcific uraemic arteriolopathy (CUA) is a serious condition in chronic kidney disease patients. Treatment combines managing mineral imbalances with wound healing therapies like hyperbaric oxygen and sodium thiosulphate.
Area of Science:
- Nephrology
- Vascular Biology
- Dermatology
Background:
- Calcific uraemic arteriolopathy (CUA), or calciphylaxis, is a rare yet significant cause of mortality in chronic kidney disease (CKD) patients.
- The incidence of CUA is rising among individuals with renal failure and is increasingly observed in non-uraemic populations.
- Understanding the molecular mechanisms of vascular calcification, particularly the uraemic microenvironment's role in smooth muscle cell differentiation into osteoblasts, is advancing.
Purpose of the Study:
- To review the current understanding and emerging treatments for calcific uraemic arteriolopathy (CUA).
- To highlight new therapeutic options for managing hyperphosphatemia and secondary hyperparathyroidism in CKD patients with CUA.
- To discuss established and novel treatment modalities for CUA.
Main Methods:
- Review of recent literature on CUA pathophysiology and treatment.
- Analysis of emerging therapies for mineral bone disorder in CKD.
- Evaluation of non-traditional CUA treatments.
Main Results:
- New treatments for hyperphosphatemia and secondary hyperparathyroidism, including bisphosphonates, novel phosphate binders, and cinacalcet, are being explored for CUA.
- Alternative CUA treatments such as hyperbaric oxygen and sodium thiosulphate show promise.
- The molecular basis of vascular calcification in CUA is increasingly understood, emphasizing the uraemic microenvironment's role.
Conclusions:
- A combined therapeutic strategy for CUA is recommended, integrating management of calcium/phosphate derangements with wound healing modalities.
- Newer agents for mineral homeostasis and established treatments like hyperbaric oxygen and sodium thiosulphate infusions should be considered.
- A significant lack of randomized controlled trials for CUA treatments persists, necessitating further research.
Purpose Of Review:
Calcific uraemic arteriolopathy (CUA) or calciphylaxis is a rare but important cause of morbidity and mortality in patients with chronic kidney disease. The prevalence of CUA is increasing in patients with renal failure, and the condition is also being recognized in nonuraemic patients.
Recent Findings:
There has been increasing understanding of the molecular basis of vascular calcification, in particular on the important role of the uraemic microenvironment in the factors implicated in the differentiation of vascular smooth muscle cells into osteoblasts. New options for treatment of hyperphosphataemia and secondary hyperparathyroidism in patients with chronic kidney disease have become available in the last few years and these have begun to be used in patients with CUA. These include bisphosphonates, newer noncalcium/nonaluminium-containing phosphate binders and case reports of use of cinacalcet. Other treatments for CUA that are not targeted directly at calcium/phosphate homeostasis include hyperbaric oxygen and the antioxidant cation chelator sodium thiosulphate.
Summary:
Clinicians managing patients with CUA should consider a combination approach of treating deranged calcium/phosphate with newer therapeutic agents and promoting wound healing with other older modalities such as hyperbaric oxygen and sodium thiosulphate infusions. Randomized controlled trials for treatments in CUA are still lacking.
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