Evaluation of Bone Metabolism Biomarkers in Paget's Disease of Bone

To evaluate serum levels of bone metabolism biomarkers in patients with Paget's disease of bone (PDB). Serum levels of osteopontin, sclerostin, receptor activator of nuclear factor kappa-Β ligand (RANKL), osteoprotegerin, Dickkopf-related protein 1 (DKK-1), and soluble frizzled-related protein...

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Veröffentlicht in:Curēus (Palo Alto, CA) CA), 2019-05, Vol.11 (5), p.e4791-e4791
Hauptverfasser: Werner de Castro, Glaucio R, Buss, Ziliani Da Silva, Rosa, Julia Salvan, Facchin, Bruno M, Fröde, Tania S
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Sprache:eng
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Zusammenfassung:To evaluate serum levels of bone metabolism biomarkers in patients with Paget's disease of bone (PDB). Serum levels of osteopontin, sclerostin, receptor activator of nuclear factor kappa-Β ligand (RANKL), osteoprotegerin, Dickkopf-related protein 1 (DKK-1), and soluble frizzled-related protein 1 (sFRP-1) were measured in 57 patients with Paget's disease of bone and 24 controls with primary osteoarthritis. Subgroup analysis was employed to identify any differences in bone metabolism biomarker levels according to disease activity or current treatment. Patients with PDB presented higher levels of osteopontin and RANKL. When compared with patients with inactive disease, patients with active disease presented higher levels of bone-specific alkaline phosphatase (BAP) and osteopontin. There was a significant correlation between serum levels of BAP and osteopontin. There was no significant correlation between levels of BAP and other bone metabolism biomarkers. Current disease extension on bone scintigraphy had a significant correlation with serum levels of osteopontin and BAP. There was no significant correlation between current disease extension and other bone metabolism biomarkers. Serum levels of osteopontin and RANKL were correlated to serum levels of BAP and disease extension. Patients with PDB presented higher levels of osteopontin and RANKL. Osteopontin could be a useful biomarker for activity and extension of PDB.
ISSN:2168-8184
2168-8184
DOI:10.7759/cureus.4791