Treatment of Osteoporosis in Patients with Chronic Kidney Disease
- PMID: 40457078
- DOI: 10.1007/s11914-025-00919-0
Treatment of Osteoporosis in Patients with Chronic Kidney Disease
Abstract
Purpose of review: To discuss current evidence on the diagnosis and management of osteoporosis in patients with chronic kidney disease (CKD).
Recent findings: Osteoporosis and fractures are prevalent in older CKD patients and associated with poor process indicators and outcomes. While osteoporosis treatment is generally similar in patients without or with CKD up to stage 3, there is still a lack of evidence to guide many areas of osteoporosis management in CKD stages 4-5. There is an urgent need to establish local multidisciplinary care pathways for CKD and dialysis patients with osteoporosis, involving nephrologists, bone specialists and fracture liaison services. Optimization of calcium and vitamin D metabolism and non-pharmacological measures including exercise and falls prevention should be considered in all patients. Withholding bone drugs solely based on glomerular filtration rates may constitute renalism (discrimination based on kidney function), which would further widen the already large treatment gap in osteoporosis. On the other hand, more evidence is needed to inform almost every aspect of anti-osteoporotic pharmacotherapy in CKD stages 4-5. The concept of choosing between antiresorptive or anabolic bone drugs based on a pre-treatment assessment of bone turnover (using biomarkers or bone biopsies), is a dogma in urgent need of critical re-evaluation. This narrative review aims to summarize our current understanding of the management of CKD-associated osteoporosis and fracture prevention in stage 4-5 CKD patients.
Keywords: Bisphosphonates; Chronic kidney disease; Denosumab; Osteoporosis; Romosozumab; Teriparatide.
© 2025. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Conflict of interest statement
Declarations. Competing interests: Dr. Laurent has received consultancy and lecture fees from Alexion, A.M. Pharma, Amgen, AstraZeneca, Galapagos, Kyowa Kirin, Menarini, Orifarm, Pharmanovia, Takeda, Sandoz, UCB and Will Pharma. Dr. Dupont has received consultancy fees and expenses from Daiichi Sankyo and UCB. Dr. Lemahieu has received consultancy fees from Astellas Pharma, Boehringer-Ingelheim and Fresenius Medical. Dr. Jamar has received travel and consultancy fees from Amgen and AstraZeneca. Dr. Mellaerts has no disclosures. Prof. Dejaeger has received research funding from UCB. Prof. Gielen has received consultancy and lecture fees from Amgen, Takeda, UCB. Prof. Evenepoel has received consultancy and lecture fees from Amgen, Fresenius Medical, Vifor, UCB, Takeda, and travel expenses from GSK.
References
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