Bone turnover markers reflect the work of the osteoclasts (bone resorption markers) and the osteoblasts (bone formation markers). These can be used to predict fracture risk and rate of bone loss, but such a use has not proven so useful clinically. However, they are very useful for monitoring therapy onset and offset.

Antiresorptive drugs such as bisphosphonates and denosumab cause a large and early decrease on bone resorption and bone formation markers and so provide an early indication of response. Anabolic drugs such as teriparatide cause a large and early increase in bone formation and bone resorption markers and so can provide an early indication of response. During a ‘drug holiday’ bone turnover markers are useful in identifying the offset of response suggesting that treatment should be resumed.

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    Professor Richard Eastell
    Professor of Bone Metabolism, University of Sheffield & Director, Mellanby Centre for Musculoskeletal Research

    Richard qualified in medicine from Edinburgh in 1977. He trained in endocrinology in Edinburgh, Northwick Park and at the Mayo Clinic (Dr B L Riggs). He leads a research group on the pathogenesis, diagnosis and treatment of osteoporosis; of particular note is his contribution to the use of bone turnover markers and the development of treatments for osteoporosis. His work has been recognised by the Philippe Bordier Award (2012) (European Calcified Tissue Society), Frederic C Bartter Award 2014 (American Society for Bone and Mineral Research), Kohn and Linda Edwards Awards from the Royal Osteoporosis Society (2004, 2018), the Clinical Endocrinology Trust Award from the European Society for Endocrinology (2020) and the Dent Lecturer from the Bone Research Society (2021).