Volume 27, Issue 9 pp. 1141-1146
Research Article
Free Access

FGF23 is a putative marker for bone healing and regeneration

Sascha Goebel

Sascha Goebel

Orthopedic Center for Musculoskeletal Research, University of Wuerzburg, Wuerzburg, Germany

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Jasmin Lienau

Jasmin Lienau

Julius Wolff Institut and Berlin-Brandenburg Center for Regenerative Therapies, Charité-Universitätsmedizin Berlin, Germany

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Ulrich Rammoser

Ulrich Rammoser

Orthopedic Center for Musculoskeletal Research, University of Wuerzburg, Wuerzburg, Germany

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Lothar Seefried

Lothar Seefried

Orthopedic Center for Musculoskeletal Research, University of Wuerzburg, Wuerzburg, Germany

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Karl Florian Wintgens

Karl Florian Wintgens

Immundiagnostik AG, Bensheim, Germany

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Jochen Seufert

Jochen Seufert

Department of Endocrinology, University of Freiburg, Freiburg, Germany

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Georg Duda

Georg Duda

Julius Wolff Institut and Berlin-Brandenburg Center for Regenerative Therapies, Charité-Universitätsmedizin Berlin, Germany

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Franz Jakob

Corresponding Author

Franz Jakob

Orthopedic Center for Musculoskeletal Research, University of Wuerzburg, Wuerzburg, Germany

Orthopedic Center for Musculoskeletal Research, University of Wuerzburg, Wuerzburg, Germany. T: ++49-931-803-1580; F: ++49-931-803-1599.Search for more papers by this author
Regina Ebert

Regina Ebert

Orthopedic Center for Musculoskeletal Research, University of Wuerzburg, Wuerzburg, Germany

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First published: 12 February 2009
Citations: 39

Abstract

Besides numerous other factors, fibroblast growth factor receptor (FGFR) signaling is involved in fracture healing and bone remodeling. FGF23 is a phosphatonin produced by osteoblastic cells, which signals via FGFR1, thereby exerting effects in bone and kidney. We analyzed if serum FGF23 levels might be an indicator to predict fracture healing and union. FGF23 (C-Term) was elevated on day 3 postoperatively in 55 patients sustaining an exchange of total hip implants due to aseptic loosening. A prospective study of 40 patients undergoing primary hip arthroplasty also showed elevated FGF23 (C-Term) but no change in FGF23 (intact) levels on days 1, 4, and 10 postoperatively. Serum phosphate and phosphate clearance stayed within normal ranges. FGF23 mRNA expression in ovine callus was compared between a standard and delayed course of osteotomy healing. In the standard model, a marked increase in FGF23 mRNA expression compared to the delayed healing situation was observed. Immunohistochemical analysis showed FGF23 production of osteoblasts and granulation tissue in the fracture callus during bone healing. In conclusion, FGF23 is involved in bone healing, can be measured by a sensitive assay in peripheral blood, and is a promising candidate as an indicator for healing processes prone to reunion versus nonunion. © 2009 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res

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