## Abstract This study was designed to explore the value of markers of bone turnover, macrophage inflammatory proteinβ1Ξ± (MIPβ1Ξ±), and osteopontin (OPN) in the diagnosis of myeloma bone disease. Twentyβfive patients with newly diagnosed and untreated multiple myeloma (MM), and 22 ageβ, sexβ, and bo
Biochemical markers of bone turnover in paget's disease of bone
β Scribed by P.D. Delmas
- Publisher
- American Society for Bone and Mineral Research
- Year
- 1999
- Tongue
- English
- Weight
- 497 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0884-0431
No coin nor oath required. For personal study only.
β¦ Synopsis
Although the measurement of total alkaline phosphatase activity in serum is a valid index to 8ssess the activity of Paget's disease of bone and to monitor treatment efficacy, this marker may lack sensitivity in some cases. Among the various markers of bone formation and resorption that have been developed, serum bone specific alkaline phosphatase and procollagen I N-terminal peptide (PINP) for formation, urinary N-telopeptide (NTX) and a-Ctelopeptide (CTX) for bone resorption have emerged as the most sensitive ones, and may be useful in the management of pagetic patients. We have recently shown that the p-isomerization of type I collagen CTX is impaired in pagetic bone matrix characterized by the existence of woven bone, as compared to normal lamellar bone matrix. This abnormality results in a preferential urinary excretion of nonisomerized (a-CTX) over p-isomerized (p-CTX) that can be measured with specific immunoassays. Patients with active Paget's disease of bone are characterized by an abnormally high cdp-CTX ratio which goes down to the normal range after bisphosphonate therapy, probably reflecting the lamellar structure of newly formed bone matrix in pagetic skeletal sites after treatment. (J
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## Abstract The karyotypes of 14 patients with Paget's disease of bone were studied. The patients were recruited from our bone metabolism clinic where they received specific therapy for their skeletal disease. Eight of the 14 patients had chromosomal translocations localized to the D and G groups.