Copyright
©The Author(s) 2015.
World J Gastroenterol. Apr 28, 2015; 21(16): 4773-4778
Published online Apr 28, 2015. doi: 10.3748/wjg.v21.i16.4773
Published online Apr 28, 2015. doi: 10.3748/wjg.v21.i16.4773
Risk factors | Ref. |
Clinical or phenotypic | |
Corticosteroid use between 12 and 6 mo before baseline | [3] |
Male gender | [3] |
Absence of previous surgical resection | [3] |
Longer disease duration from diagnosis to first infliximab | [7] |
Previous biological therapy | [11-13] |
Dose intensification during the first year of anti-TNFα therapy | [11] |
Age at CD diagnosis ≥ 25 yr | [6] |
Ileocolonic disease at diagnosis | [12] |
Active smoking | [5] |
Previous antimetabolite failure | [5] |
Perianal disease | [5] |
Serological1 | |
Hemoglobin levels ≤ 14.5 g/dL | [3] |
White blood count > 6 × 109/L | [3] |
High sensitive CRP ≥ 5 mg/L | [3] |
Infliximab trough levels ≥ 2 μg/mL | [3] |
Serum calprotectin > 5675 ng/mL | [37] |
Endoscopic1 | |
CDEIS > 0 | [3] |
Mucosal1 | |
Lack of normalization of IL-17A and TNFα expression levels | [10] |
Microbiological1 (CD-associated dysbiosis) | |
Low rate of Faecalibacterium prausnitzii in fecal samples | [38] |
Low rate of Bacteroides in fecal samples | [38] |
Fecal1 | |
Fecal calprotectin ≥ 300 μg/g | [3] |
Genetic | |
Fc gamma receptor IIIB-NA2/NA2 genotype (fistulising disease) | [39] |
- Citation: Papamichael K, Vermeire S. Withdrawal of anti-tumour necrosis factor α therapy in inflammatory bowel disease. World J Gastroenterol 2015; 21(16): 4773-4778
- URL: https://www.wjgnet.com/1007-9327/full/v21/i16/4773.htm
- DOI: https://dx.doi.org/10.3748/wjg.v21.i16.4773