4.8 Article

Clinical disease activity, C-reactive protein normalisation and mucosal healing in Crohn's disease in the SONIC trial

期刊

GUT
卷 63, 期 1, 页码 88-95

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/gutjnl-2013-304984

关键词

INFLAMMATORY BOWEL DISEASE

资金

  1. Merck
  2. Abbott
  3. Janssen
  4. Genentech
  5. Mitsubishi
  6. Ferring
  7. Ferring, Norgine
  8. Tillots
  9. Vifor
  10. Shire
  11. Therakos
  12. Pharmacosmos
  13. Pilege
  14. BMS
  15. UCB-pharma
  16. Hospira
  17. Takeda
  18. MSD
  19. FALK Foundation
  20. Angelini
  21. Schering-Plough Hellas
  22. Abbott Hellas

向作者/读者索取更多资源

Background and aims The Crohn's Disease Activity Index (CDAI) has been criticised due to heavy weighting on subjective clinical symptoms. C-reactive protein (CRP) and endoscopic lesions are objective measures of inflammation. We investigated the relationships between clinical disease activity, CRP normalisation and mucosal healing in Crohn's disease (CD). Methods The Study of Biologic and Immunomodulator Naive Patients in CD trial compared infliximab to azathioprine and to infliximab plus azathioprine in 508 CD patients. Mucosal healing was defined as the absence of mucosal ulceration at the week 26 ileocolonoscopy in a patient who had evidence of ulceration at the baseline ileocolonoscopy. Results 188 patients who had evaluable ileocolonoscopy with evidence of mucosal ulceration at baseline, CDAI scores and CRP values at baseline and week 26 were analysed. Seventy-two of 136 patients (53%) who had a CDAI<150 at week 26 achieved mucosal healing, and 38 of 90 patients (42%) achieved both CRP normalisation (CRP<0.8mg/dL) and mucosal healing while in clinical remission. The positive predictive value (PPV) and negative predictive value (NPV) of CDAI to detect mucosal healing using 150 as a cut-off for CDAI were 65% and 53%, respectively. The PPV and NPV of CDAI to detect mucosal healing and CRP normalisation using 150 as a cut-off for CDAI were 79% and 42%, respectively. Conclusions Half the patients under azathioprine and/or infliximab in clinical remission have endoscopic and/or CRP evidence of residual active CD, whereas other patients with endoscopic and CRP normalisation have persistent clinical symptoms. Clinical symptoms as scored by CDAI are not a reliable measure of the underlying inflammation.

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