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Types I and III procollagen extension peptides in serum respond to fracture in humans.

Authors
  • Joerring, S
  • Jensen, L T
  • Andersen, G R
  • Johansen, J S
Type
Published Article
Journal
Archives of orthopaedic and trauma surgery
Publication Date
Jan 01, 1992
Volume
111
Issue
5
Pages
265–267
Identifiers
PMID: 1389778
Source
Medline
License
Unknown

Abstract

Markers of types I and III collagen turnover were measured in serial blood samples in 16 patients with a Colles' fracture. The collagen markers were the carboxy-terminal extension peptide of type I procollagen (PICP) and the amino-terminal extension peptide of type III procollagen (PIIINP). Significant increases were found of PIIINP within 1 week and of PICP within 2 weeks. This sequential appearance of PIIINP and PICP was found to be in agreement with the appearance of types III and I collagen during early fracture healing as demonstrated in previous animal experimental studies. PICP had levelled off after 9 months, whereas PIIINP remained elevated. Osteocalcin, a serum marker of osteoblast activity, increased within 1 week and levelled off after 9 months. Correlations between the change in osteocalcin and those in PICP and PIIINP, respectively, were weak. These new biochemical markers may prove relevant as non-invasive markers of normal and pathological fracture healing in humans.

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