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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Assessing bone mineralisation in children with chronic kidney disease: what clinical and research tools are
A D Lalayiannis1, N J Crabtree2, M Fewtrell3
1Nephrology Department Great Ormond St. Hospital for Children NHS Foundation Trust and University College London Institute of Child Health, London, UK. alex.lalayiannis@nhs.net.
Insights
Mineral and bone disorder in chronic kidney disease (CKD-MBD) affects children, causing bone issues and calcification. Current management relies on serum markers, as imaging and bone biopsy are mainly research tools.
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Bone Metabolism
Background:
- Chronic kidney disease-mineral and bone disorder (CKD-MBD) involves imbalances in calcium, phosphate, PTH, and vitamin D, leading to bone abnormalities and soft tissue calcification.
- Optimal bone health in pediatric CKD is crucial for preventing fractures, optimizing growth, and avoiding vascular calcification.
Purpose of the Study:
- To review normal bone mineralization processes.
- To explore the pathophysiology of dysregulated homeostasis in CKD-MBD and its clinical impact.
- To assess available tools for evaluating bone mineral density in pediatric CKD.
Main Methods:
- Overview of bone histology and histomorphometry as gold standards for assessing bone mineralization.
- Discussion of imaging techniques: dual-energy X-ray absorptiometry (DXA) and peripheral quantitative computed tomography (pQCT).
- Review of serum biomarkers and their relationship to bone histomorphometry.
Main Results:
- Bone histology is the definitive assessment but rarely performed in clinical practice.
- DXA and pQCT offer insights into bone mineral density but have limitations in pediatric CKD.
- Current clinical management predominantly relies on serum calcium, phosphate, PTH, vitamin D, and alkaline phosphatase levels due to limited evidence for other methods.
Conclusions:
- Bone imaging and histology are primarily research tools in pediatric CKD.
- Clinical decisions for managing CKD-MBD in children are guided by biochemical markers.
- Further research is needed to establish the clinical utility of advanced imaging and biopsy in this population.
Abstract:
Mineral and bone disorder in chronic kidney disease (CKD-MBD) is a triad of biochemical imbalances of calcium, phosphate, parathyroid hormone and vitamin D, bone abnormalities and soft tissue calcification. Maintaining optimal bone health in children with CKD is important to prevent long-term complications, such as fractures, to optimise growth and possibly also to prevent extra-osseous calcification, especially vascular calcification. In this review, we discuss normal bone mineralisation, the pathophysiology of dysregulated homeostasis leading to mineralisation defects in CKD and its clinical consequences. Bone mineralisation is best assessed on bone histology and histomorphometry, but given the rarity with which this is performed, we present an overview of the tools available to clinicians to assess bone mineral density, including serum biomarkers and imaging such as dual-energy X-ray absorptiometry and peripheral quantitative computed tomography. We discuss key studies that have used these techniques, their advantages and disadvantages in childhood CKD and their relationship to biomarkers and bone histomorphometry. Finally, we present recommendations from relevant guidelines-Kidney Disease Improving Global Outcomes and the International Society of Clinical Densitometry-on the use of imaging, biomarkers and bone biopsy in assessing bone mineral density. Given low-level evidence from most paediatric studies, bone imaging and histology remain largely research tools, and current clinical management is guided by serum calcium, phosphate, PTH, vitamin D and alkaline phosphatase levels only.
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