[Serum bone marker measurements in bone metabolism disorders associated with inflammatory bowel diseases]

Orv Hetil. 2001 Jul 22;142(29):1557-60.
[Article in Hungarian]

Abstract

Patients with inflammatory bowel disease (IBD) have decreased bone mineral density (BMD), which is usually much more remarkable in patients with Crohn's disease (CD) than those with ulcerative colitis (UC). The aim of the present study was to investigate the usefulness of serum beta-Crosslaps (bCL) and osteocalcin (OC) determinations to assess bone metabolism in patients with IBD. Forty-nine patients with IBD (23 UC, 26 CD) and 46 healthy controls were studied. Serum bCL and OC were measured by Elecsys immunoassay. Compared to controls (0.275 +/- 0.14 ng/ml) the mean bCL concentration was significantly higher in the CD (mean = 0.489 +/- 0.25 ng/ml; p < 0.001) and UC groups (mean = 0.439 +/- 0.3 ng/ml; p < 0.01). The mean OC concentration was significantly higher in the CD group (28.52 +/- 14.75 ng/ml) than in controls (21.42 +/- 7.43 ng/ml) but OC level was not significantly increased in the UC group (24.89 +/- 15.08 ng/ml). There was no significant difference in bCL or OC concentrations between the CD and UC groups. These results indicate that the accelerated bone resorption is not associated with increased bone formation in patients with IBD. These two marker of the bone metabolism could be a good laboratory parameter of bone pathology in patients with IBD, especially in CD.

Publication types

  • English Abstract

MeSH terms

  • Adult
  • Biomarkers / blood
  • Body Mass Index
  • Bone Density
  • Bone and Bones / metabolism*
  • Case-Control Studies
  • Colitis, Ulcerative / complications
  • Colitis, Ulcerative / metabolism
  • Collagen / blood*
  • Crohn Disease / complications
  • Crohn Disease / metabolism
  • Female
  • Humans
  • Inflammatory Bowel Diseases / blood
  • Inflammatory Bowel Diseases / complications*
  • Inflammatory Bowel Diseases / metabolism*
  • Male
  • Middle Aged
  • Osteocalcin / blood*
  • Peptide Fragments / blood*

Substances

  • Biomarkers
  • Peptide Fragments
  • glutamyl-lysyl-alanyl-histidyl-aspartyl-glycyl-glycyl-arginine
  • Osteocalcin
  • Collagen