Management of Osteoporosis and Low Bone Mass in Kidney Disease

Chronic kidney disease (CKD) is associated with increased fracture risk and post-fracture mortality. CKD-associated osteoporosis arises from the combined effects of traditional pathways (e.g., age-related bone loss) and CKD-specific mechanisms (e.g., disturbances in mineral metabolism) that contribute to bone fragility. Dual-energy X-ray absorptiometry (DXA), serum calcium, phosphorus, 25-hydroxyvitamin D, parathyroid hormone (PTH), and bone turnover markers that are not cleared by the kidneys are used to assess bone health in patients with CKD. Bone biopsy may be used to directly assess bone turnover, mineralization and volume to guide treatment in patients with advanced CKD. Antiresorptive and anabolic therapies for osteoporosis have demonstrated efficacy and safety in mild to moderate stages of CKD, but there are limited data to guide the use of these drugs in CKD stages 4-5. Oral bisphosphonates and denosumab may be effective in advanced CKD, but no study to date has demonstrated a fracture risk reduction in this group. Hypocalcemia and other safety concerns limit the use of denosumab in patients with advanced CKD. PTH analogues and romosozumab demonstrate improvements in bone mineral density in CKD stages 4-5, but more data is needed to support the use of these drugs in this population.

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Publication Details

Journal
Clinical Journal of the American Society of Nephrology
Published
2026-06-16
DOI
https://doi.org/10.2215/cjn.0000001149
Primary Topic
Parathyroid Disorders and Treatments
Type
article
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article

Management of Osteoporosis and Low Bone Mass in Kidney Disease

Albert Shieh, Matthew C Mulroy, Isidro B. Salusky, Angela Primbas et al.
Clinical Journal of the American Society of Nephrology
Parathyroid Disorders and Treatments
article

Management of Osteoporosis and Low Bone Mass in Kidney Disease

Albert Shieh, Matthew C Mulroy, Isidro B. Salusky, Angela Primbas, Jane Weinreb
article en

Abstract

Chronic kidney disease (CKD) is associated with increased fracture risk and post-fracture mortality. CKD-associated osteoporosis arises from the combined effects of traditional pathways (e.g., age-related bone loss) and CKD-specific mechanisms (e.g., disturbances in mineral metabolism) that contribute to bone fragility. Dual-energy X-ray absorptiometry (DXA), serum calcium, phosphorus, 25-hydroxyvitamin D, parathyroid hormone (PTH), and bone turnover markers that are not cleared by the kidneys are used to assess bone health in patients with CKD. Bone biopsy may be used to directly assess bone turnover, mineralization and volume to guide treatment in patients with advanced CKD. Antiresorptive and anabolic therapies for osteoporosis have demonstrated efficacy and safety in mild to moderate stages of CKD, but there are limited data to guide the use of these drugs in CKD stages 4-5. Oral bisphosphonates and denosumab may be effective in advanced CKD, but no study to date has demonstrated a fracture risk reduction in this group. Hypocalcemia and other safety concerns limit the use of denosumab in patients with advanced CKD. PTH analogues and romosozumab demonstrate improvements in bone mineral density in CKD stages 4-5, but more data is needed to support the use of these drugs in this population.

Clinical Journal of the American Society of Nephrology
University of California, Los Angeles (US), University of California System (US), Stanford Health Care (US), Primary Health Care (QA), VA Greater Los Angeles Healthcare System (US)
Good health and well-being
Openalex Percentile: Top 7%
Parathyroid Disorders and Treatments
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