Abstract
Glucocorticoids (GCs) remain as the cornerstone of therapy in most inflammatory diseases, even if newly developed biological molecules became available. GCs are potent, possess a fast action, and are cheap and relatively easy to prescribe. However, their beneficial therapeutic activity has a nasty counterpart: quite a lot of complications, notably secondary osteoporosis, aseptic bone osteonecrosis, and fractures. The skeleton is continuously remodeling, old bone being resorbed and replaced by new young bone. GCs interfere with the bone turnover and provoke a disequilibrium in favor of bone loss and fragility. The mechanisms of bone fragility consist of a decreased activity and in apoptosis of osteoblasts, as well as an increase in bone resorption. These changes have already been observed histomorphometrically a long time ago in transiliac bone biopsies. Biological parameters of bone turnover, chiefly degradation products of type I collagen, can help to assess atraumatically the bone metabolism. If, in idiopathic osteoporosis, they can have a predictive value of bone loss, they cannot be considered as surrogates for bone mineral density measurements. In GC-OP, the concentrations of the bone turnover markers (BTMs) of bone formation dramatically and rapidly decrease, whereas the BTMs of bone resorption slightly increase. During GC therapy, they cannot be used as predictive tools of bone fragility on an individual basis. Other markers such as RANKL/RANK/osteoprotegerin seem to be promising in this aim, but this still awaits confirmation.
Abbreviations
- ALN:
-
Alendronate
- BDP:
-
Beclomethasone dipropionate
- BMD:
-
Bone mineral density
- BSAP:
-
Bone-specific alkaline phosphatase
- BTMs:
-
Bone turnover markers
- BUD:
-
Budenoside
- CD:
-
Crohn’s disease
- COMP:
-
Cartilage oligomeric matrix protein
- COPD:
-
Chronic obstructive pulmonary disease
- CTX:
-
Carboxy-terminal cross-linking telopeptide of type I collagen
- DAS:
-
Disease activity score
- Dkk-1:
-
Dickkopf-1
- FN:
-
Femoral neck
- GC:
-
Glucocorticoid
- ICTP:
-
Carboxy-terminal telopeptide of type I collagen
- Il-6:
-
Interleukin-6
- JIA:
-
Juvenile idiopathic arthritis
- MMP:
-
Metalloproteinase
- MP:
-
Methylprednisolone
- NTX:
-
Amino-terminal cross-linking telopeptide of type I collagen
- OBS:
-
Osteoblasts
- OC:
-
Osteocalcin
- OCS:
-
Osteoclasts
- OP:
-
Osteoporosis
- OPG:
-
Osteoprotegerin
- PICP:
-
Procollagen type I C-terminal propeptide
- PINP:
-
Procollagen type I N-terminal propeptide
- PTH:
-
Parathyroid hormone
- RA:
-
Rheumatoid arthritis
- RANK:
-
Receptor activator of nuclear factor NF-kB
- RANK-L:
-
Receptor activator of nuclear factor NF-kB-ligand
- rh:
-
Recombinant human
- RIS:
-
Risedronate
- Scl:
-
Sclerostin
- SLE:
-
Systemic lupus erythematosus
- TPTD:
-
Teriparatide
- TRAP:
-
Tartrate-resistant acid phosphatase
- UC:
-
Ulcerative colitis
- uDPD:
-
Urinary deoxypyridinoline
- uPYD:
-
Urinary pyridinoline
- VF:
-
Vertebral fracture
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Devogelaer, JP., Durnez, A., Gruson, D., Manicourt, D.H. (2015). Bone Turnover Markers and Glucocorticoid Treatments. In: Preedy, V. (eds) Biomarkers in Bone Disease. Biomarkers in Disease: Methods, Discoveries and Applications. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-7745-3_23-1
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DOI: https://doi.org/10.1007/978-94-007-7745-3_23-1
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