4.5 Article

Patients with Crohn's Disease with High Body Mass Index Present More Frequent and Rapid Loss of Response to Infliximab

期刊

INFLAMMATORY BOWEL DISEASES
卷 23, 期 10, 页码 1853-1859

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MIB.0000000000001179

关键词

Crohn's disease; infliximab; body mass index; therapeutic strategy

资金

  1. MSD
  2. Abbvie
  3. Takeda
  4. Hospira
  5. Ferring
  6. Shire Pharmaceuticals
  7. UCB Phama
  8. Norgne
  9. Pileje
  10. Biofortis
  11. Giuliani SpA
  12. Roquette
  13. Txcell
  14. Lesaffre
  15. Norgine
  16. Genfit
  17. OmegaPharma International
  18. Ppm
  19. Kitozyme
  20. LFB
  21. Boehringer Ingelheim
  22. Intralytix
  23. Janssen
  24. Pfizer
  25. Biogram

向作者/读者索取更多资源

Background: Infliximab (IFX) is effective in inducing and maintaining remission in patients with luminal and anoperineal Crohn's disease (CD). However, treatment failure within 12 months after initiating IFX is observed in a significant proportion of patients. The aim of the present study was to determine whether the body mass index (BMI) affects response to IFX during the first year of treatment in patients with CD. Methods: All patients with luminal CD who began IFX between January 2010 and May 2014 were prospectively included. BMI was calculated before IFX treatment was begun, and patients were divided into 3 groups: normal BMI (BMI, 25 kg/m(2)), overweight patients (BMI of 25.0-30 kg/m(2)), and obese patients (BMI >30.0 kg/m(2)). The primary outcome was to evaluate the rate and delay of IFX optimization during the first year of treatment among normal weight, overweight, and obese patients. Results: One hundred forty patients were included. Demographic and clinical characteristics at IFX initiation were comparable among the 3 groups. Within 12 months after the initiation of IFX, the rate of IFX optimization was significantly higher in overweight and obese patients than in the normal BMI group: 52%, 56%, and 20%, respectively (P = 0.0002). The median time until optimization of IFX was significantly shorter in overweight and obese patients than in the normal BMI group: 7, 7, and 10 months, respectively (P = 0.03). A BMI >25 kg/m(2) was significantly associated with IFX optimization within 12 months on multivariate analysis. Conclusion: This is the first study to show that optimization of IFX is more frequent and faster in obese and overweight patients with CD and occurs within 12 months after beginning IFX, suggesting that an induction regimen with higher doses of IFX and a tight control of IFX concentrations may be needed in these patients.

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