TY - JOUR
T1 - Serum C-reactive protein and albumin are useful biomarkers for tight control management of Crohn’s disease in Japan
AU - Shiga, Hisashi
AU - Abe, Izuru
AU - Onodera, Motoyuki
AU - Moroi, Rintaro
AU - Kuroha, Masatake
AU - Kanazawa, Yoshitake
AU - Kakuta, Yoichi
AU - Endo, Katsuya
AU - Kinouchi, Yoshitaka
AU - Masamune, Atsushi
N1 - Funding Information:
Subjects.? We reviewed the treatment course of consecutive patients with CD who were naïve to biologics and were treated with anti-TNF agents at the Tohoku University Hospital between July 2003 and September 2018. CD was diagnosed based on the diagnostic criteria proposed by the Research Group of Intractable Inflammatory Bowel Disease under the aegis of the Ministry of Health, Labor and Welfare of Japan10. Patients were included irrespective of the disease location or disease behavior. We excluded patients who discontinued treatment with anti-TNF agents for some reasons within 8 weeks. The Ethics Committee of the Tohoku University Hospital approved the study; the clinical procedures were carried out in accordance with the Declaration of Helsinki. Written informed consent was obtained from all patients.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Tight control management of Crohn’s disease (CD) based on biomarkers is more effective than conventional clinical management; however, fecal calprotectin is not allowed in Asian and some Western countries. To investigate whether tight control management based on readily available serum biomarkers results in better outcomes, we retrospectively reviewed treatment courses of consecutive Japanese CD patients treated with anti-tumor necrosis factor agents between 2003 and 2018. The association between failure of tight control (C-reactive protein (CRP) ≥ 0.5 mg/dL or albumin (Alb) < 3.8 g/dL at week 8 or 24) and subsequent major adverse outcomes (MAOs; hospitalization related to CD worsening, surgery, and discontinuation due to treatment failure) were analyzed. Among 223 patients followed for >8 weeks, 88 patients experienced MAOs. Multivariate analysis identified penetrating type, CRP ≥ 0.5 mg/dL and Alb < 3.8 g/dL at week 8 as independent risk factors (hazard ratios: 2.16, 2.06, and 2.08, respectively). Among 204 patients followed for >24 weeks, 80 patients experienced MAOs. Penetrating type, CRP ≥ 0.5 mg/dL, and Alb < 3.8 g/dL at week 24 were identified as independent risk factors (2.39, 1.90, and 2.20, respectively). Even in settings without fecal calprotectin, tight control management based on serum CRP and Alb may help avoid MAOs.
AB - Tight control management of Crohn’s disease (CD) based on biomarkers is more effective than conventional clinical management; however, fecal calprotectin is not allowed in Asian and some Western countries. To investigate whether tight control management based on readily available serum biomarkers results in better outcomes, we retrospectively reviewed treatment courses of consecutive Japanese CD patients treated with anti-tumor necrosis factor agents between 2003 and 2018. The association between failure of tight control (C-reactive protein (CRP) ≥ 0.5 mg/dL or albumin (Alb) < 3.8 g/dL at week 8 or 24) and subsequent major adverse outcomes (MAOs; hospitalization related to CD worsening, surgery, and discontinuation due to treatment failure) were analyzed. Among 223 patients followed for >8 weeks, 88 patients experienced MAOs. Multivariate analysis identified penetrating type, CRP ≥ 0.5 mg/dL and Alb < 3.8 g/dL at week 8 as independent risk factors (hazard ratios: 2.16, 2.06, and 2.08, respectively). Among 204 patients followed for >24 weeks, 80 patients experienced MAOs. Penetrating type, CRP ≥ 0.5 mg/dL, and Alb < 3.8 g/dL at week 24 were identified as independent risk factors (2.39, 1.90, and 2.20, respectively). Even in settings without fecal calprotectin, tight control management based on serum CRP and Alb may help avoid MAOs.
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U2 - 10.1038/s41598-020-57508-7
DO - 10.1038/s41598-020-57508-7
M3 - Article
C2 - 31949246
AN - SCOPUS:85077940902
SN - 2045-2322
VL - 10
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 511
ER -