Response to medical treatment in patients with Crohn's disease: the role of NOD2/CRAD15, disease phenotype, and age of diagnosis

Dig Dis Sci. 2010 Jun;55(6):1674-80. doi: 10.1007/s10620-009-0936-8. Epub 2009 Aug 20.

Abstract

Purpose: Factors influencing response to medications in Crohn's disease (CD) patients are not fully understood. We aimed to evaluate the relationships between NOD2/CARD15 mutations, disease phenotype and age of CD diagnosis and response to medical treatment with systemic steroids, azathioprine (AZA) or 6-mercaptopurine (6-MP), and infliximab.

Methods: A retrospective medical records analysis was made of patients previously tested for the CD-associated NOD2/CARD15 mutations. Harvey- Bradshaw score was used to assess remission or response to therapy.

Results: CD-associated NOD2/CARD15 mutations were not related to the rate of steroids dependency or clinical response to AZA/6-MP and infliximab. Steroid dependency was associated with colonic involvement. Thirty-three of 127 (26%) patients with colonic disease were steroid dependent, compared with 7/72 (9.7%) patients with isolated small bowel disease (ISBD), (p = 0.009). ISBD was mildly associated with a better remission/response to AZA/6-MP treatment. Disease behavior and age of diagnosis were not related to response to therapy.

Conclusions: Response to treatment with systemic steroids, AZA/6-MP and infliximab are not related to NOD2/CARD15 mutations, age of diagnosis and disease behavior. Patients with colonic disease have higher rates of steroid dependency.

Publication types

  • Multicenter Study

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Anti-Inflammatory Agents / therapeutic use*
  • Antibodies, Monoclonal / therapeutic use
  • Azathioprine / therapeutic use
  • Chi-Square Distribution
  • Crohn Disease / diagnosis
  • Crohn Disease / drug therapy*
  • Crohn Disease / genetics
  • Female
  • Gastrointestinal Agents / therapeutic use*
  • Genetic Predisposition to Disease
  • Humans
  • Infliximab
  • Israel
  • Longitudinal Studies
  • Male
  • Mercaptopurine / therapeutic use
  • Middle Aged
  • Mutation*
  • Nod2 Signaling Adaptor Protein / genetics*
  • Phenotype
  • Retrospective Studies
  • Steroids / therapeutic use
  • Treatment Outcome
  • Young Adult

Substances

  • Anti-Inflammatory Agents
  • Antibodies, Monoclonal
  • Gastrointestinal Agents
  • NOD2 protein, human
  • Nod2 Signaling Adaptor Protein
  • Steroids
  • Infliximab
  • Mercaptopurine
  • Azathioprine