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The importance of bone biopsy in chronic kidney disease-Mineral bone disorders
Periklis Dousdampanis1, Kostantina Trigka1
1Hemodialysis Unit Kyanos Stavros, Patras, Greece.
Insights
Renal osteodystrophy (ROD), now termed CKD-mineral and bone disorder (CKD-MBD), requires precise diagnosis. Bone biopsy is ideal but impractical, necessitating research into specific biomarkers for better management of bone disease in chronic kidney disease patients.
Area of Science:
- Nephrology
- Endocrinology
- Bone Metabolism
Background:
- Renal osteodystrophy (ROD) is a complex group of bone diseases stemming from chronic kidney disease (CKD).
- The term CKD-mineral and bone disorder (CKD-MBD) encompasses a broader spectrum than traditional ROD.
- Current biomarkers like parathyroid hormone (PTH) and alkaline phosphatase may not accurately reflect bone turnover in CKD-MBD.
Purpose of the Study:
- To highlight the limitations of current diagnostic methods for CKD-MBD.
- To emphasize the diagnostic value of bone biopsy despite its clinical limitations.
- To advocate for the development of specific biomarkers for CKD-MBD.
Main Methods:
- Review of existing literature on ROD and CKD-MBD.
- Analysis of the diagnostic utility of bone biopsy versus non-invasive markers.
- Discussion of the challenges and potential future directions for biomarker research.
Main Results:
- Bone biopsy offers precise histopathological information crucial for diagnosing CKD-MBD.
- Non-invasive biomarkers and tools often lack the specificity required for accurate diagnosis.
- Clinical application of bone biopsy is limited due to invasiveness and lack of nephrologist training.
Conclusions:
- Accurate diagnosis of CKD-MBD is essential for effective therapeutic strategies.
- The impracticality of bone biopsy necessitates the urgent study of novel, specific biomarkers.
- Developing reliable biomarkers is key to improving the management of bone disease in CKD.
Abstract:
Renal osteodystrophy (ROD) is not a uniform bone disease; it is a heterogeneous group of metabolic bone diseases due to chronic kidney disease (CKD). The traditional term of ROD does not accurately include the wide spectrum of "CKD-mineral and bone disorder" (CKD-MBD) and has been restricted to define the several specific histologic disturbances of bone disease associated with CKD. Circulating parathyroid hormone (PTH) and total alkaline phosphatase levels do not always reflect bone turnover in CKD-MBD, whereas bone biopsy provides precise information regarding bone pathology. Given the lack of specificity of several biomarkers and noninvasive tools regarding ROD, bone biopsy is required for precise diagnosis and for the determination of therapeutic strategies. In clinical practice, bone biopsy is not performed due to lack of enthusiasm among nephrologists for several reasons including the invasiveness of the procedure, the potential pain, and lack of technical training. Since the application of bone biopsy in clinical practice is unrealistic, several biomarkers with specificity for bone disease should be studied.
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