An open-label trial of the PPAR-gamma ligand rosiglitazone for active ulcerative colitis

Am J Gastroenterol. 2001 Dec;96(12):3323-8. doi: 10.1111/j.1572-0241.2001.05333.x.

Abstract

Objectives: Previous research has demonstrated that ligands for the gamma subtype of peroxisome proliferator-activated receptors (PPARs) reduce inflammation in two different murine models of colitis. This study was designed to examine the potential efficacy of rosiglitazone, a ligand for the gamma subtype of PPARs, as a therapy for active ulcerative colitis.

Methods: Fifteen patients with mild to moderately active ulcerative colitis despite therapy with 5-aminosalicylic acid compounds were enrolled in an open-label study of rosiglitazone (4 mg b.i.d. p.o.) for 12 wk. Thirteen of 15 patients were receiving concomitant therapy with corticosteroids and/or immunomodulator medications. Disease activity was measured with the Disease Activity Index.

Results: After 12 wk of therapy, four patients (27%) had achieved clinical remission, of whom three (20%) also had an endoscopic remission. Four additional patients (27%) had a clinical response without achieving remission. Two patients were hospitalized with worsened disease activity, and one patient was withdrawn for nephrotic syndrome.

Conclusions: These data suggest that ligands for the gamma subtype of PPARs may represent a novel therapy for ulcerative colitis. A double blind, placebo-controlled, randomized trial is warranted.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Colitis, Ulcerative / drug therapy*
  • Colitis, Ulcerative / pathology
  • Colitis, Ulcerative / physiopathology*
  • Colonoscopy
  • Female
  • Humans
  • Ligands
  • Male
  • Middle Aged
  • Prospective Studies
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Remission Induction
  • Rosiglitazone
  • Severity of Illness Index
  • Thiazoles / adverse effects
  • Thiazoles / metabolism*
  • Thiazoles / therapeutic use*
  • Thiazolidinediones*
  • Transcription Factors / metabolism*

Substances

  • Ligands
  • Receptors, Cytoplasmic and Nuclear
  • Thiazoles
  • Thiazolidinediones
  • Transcription Factors
  • Rosiglitazone