Rapid improvement of bone metabolism after infliximab treatment in Crohn's disease

Aliment Pharmacol Ther. 2004 Sep 15;20(6):607-14. doi: 10.1111/j.1365-2036.2004.02152.x.

Abstract

Background: Crohn's disease is associated with low bone mineral density and altered bone metabolism.

Aim: To assess the evolution of bone metabolism in Crohn's disease patients treated with infliximab.

Methods: We studied 71 Crohn's disease patients treated for the first time with infliximab for refractory Crohn's disease. Biochemical markers of bone formation (type-I procollagen N-terminal propeptide, bone-specific alkaline phosphatase, osteocalcin) and of bone resorption (C-telopeptide of type-I collagen) were measured in the serum before and 8 weeks after infliximab therapy and compared with values in a matched healthy control group.

Results: Eight weeks after treatment with infliximab, a normalization of bone markers was observed with a median increase in formation markers of 14-51% according to marker and a lower but significant decrease in resorption marker (median 11%). A clinically relevant increase in bone formation markers was present in 30-61% of patients according to the marker. A clinically relevant decrease in C-telopeptide of type-I collagen was present in 38% of patients. No association was found with any tested demographic or clinical parameter.

Conclusion: Infliximab therapy in Crohn's disease may rapidly influence bone metabolism by acting either on bone formation or bone resorption. This improvement seems to be independent of clinical response to infliximab.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antibodies, Monoclonal / therapeutic use*
  • Biomarkers / blood
  • Bone Density / physiology*
  • Bone Resorption / etiology
  • Bone Resorption / metabolism
  • Bone and Bones / metabolism*
  • Crohn Disease / drug therapy*
  • Crohn Disease / metabolism
  • Female
  • Gastrointestinal Agents / therapeutic use*
  • Humans
  • Infliximab
  • Male
  • Middle Aged
  • Osteogenesis / physiology

Substances

  • Antibodies, Monoclonal
  • Biomarkers
  • Gastrointestinal Agents
  • Infliximab