MMP mediated type V collagen degradation (C5M) is elevated in ankylosing spondylitis

Clin Biochem. 2012 May;45(7-8):541-6. doi: 10.1016/j.clinbiochem.2012.02.007. Epub 2012 Feb 21.

Abstract

Objectives: Type V collagen has been demonstrated to control fibril formation. The aim of this study was to develop an ELISA capable of detecting a fragment of type V collagen generated by MMP-2/9 and to evaluate the assay as biomarker for ankylosing spondylitis (AS).

Design and methods: A fragment unique to type V collagen and generated by both MMP-2/9 cleaved at the amino acid position 1317 (C5M) was selected for ELISA development. 40 AS patients and 40 age-matched controls were evaluated.

Results: An ELISA detecting C5M with inter- and intra-assay variations of 9.1% and 4.4% was developed. C5M levels were significantly higher in AS patients compared to controls, 229% (p<0.0001). The diagnostic AUC was 83%.

Conclusions: This ELISA is the first for detecting type V collagen degradation. AS patients had highly elevated levels of MMP mediated type V collagen degradation. The prognostic and diagnostic values need to be further investigated in additional clinical settings.

Publication types

  • Evaluation Study

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Animals
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / metabolism
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Case-Control Studies
  • Collagen Type VI / blood*
  • Collagen Type VI / metabolism
  • Enzyme-Linked Immunosorbent Assay / methods*
  • Female
  • Humans
  • Male
  • Matrix Metalloproteinase 2 / metabolism*
  • Matrix Metalloproteinase 9 / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Middle Aged
  • Peptide Fragments
  • Prognosis
  • Proteolysis
  • Retrospective Studies
  • Spondylitis, Ankylosing / diagnosis
  • Spondylitis, Ankylosing / metabolism
  • Spondylitis, Ankylosing / pathology*
  • Young Adult

Substances

  • Antibodies, Monoclonal
  • Biomarkers
  • Collagen Type VI
  • Peptide Fragments
  • MMP2 protein, human
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9