TY - JOUR
T1 - Terminal ileum thickness during maintenance therapy is a predictive marker of the outcome of infliximab therapy in crohn disease
AU - Albshesh, Ahmad
AU - Ungar, Bella
AU - Horin, Shomron Ben
AU - Eliakim, Rami
AU - Kopylov, Uri
AU - Carter, Dan
N1 - Publisher Copyright:
© 2020 Oxford University Press. All rights reserved.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Background: Mucosal healing has been associated with long-Term response to therapy for Crohn disease (CD). However, little is known about the significance of terminal ileum (TI) transmural thickness in predicting clinical outcomes. Methods: In this retrospective observational cohort study, we examined the association of an index ultrasonographic assessment of TI thickness during the maintenance phase and the subsequent clinical outcome of CD in a cohort of patients treated with infliximab (IFX). Treatment failure was defined as treatment discontinuation because of lack of efficacy, a need for dose escalation, or surgery. Clinical response was defined as treatment continuation in the absence of any of the aforementioned failure criteria. Results: Sixty patients with CD receiving IFX therapy were included in the study. The patients were followed for a median of 16 months (5-24 months) after an index intestinal ultrasound. Thirty-eight patients (63.3%) maintained response to the therapy and 22 patients (36.6%) failed the treatment, with a mean follow up of 10.5 months (6.5-17 months) vs 9.25 months (1-10.25 months), respectively. On univariate analysis, the only variables differing between treatment response and failure were a TI thickness of 2.8 vs 5 mm (P 0.0001) and an IFX trough level of 6.6 vs 3.9 ug/mL (P = 0.008). On multivariable analysis, only a small bowel thickness of 4 mm was associated with the risk of treatment failure (odds ratio, 2.9; 95% CI, 1.49-5.55; P = 0.002). Conclusions: Our findings suggest that transmural thickness of 4 mm can predict subsequent treatment failure in patients with CD treated using IFX, indicating transmural thickness 4 mm as a potential novel valuable therapeutic target.
AB - Background: Mucosal healing has been associated with long-Term response to therapy for Crohn disease (CD). However, little is known about the significance of terminal ileum (TI) transmural thickness in predicting clinical outcomes. Methods: In this retrospective observational cohort study, we examined the association of an index ultrasonographic assessment of TI thickness during the maintenance phase and the subsequent clinical outcome of CD in a cohort of patients treated with infliximab (IFX). Treatment failure was defined as treatment discontinuation because of lack of efficacy, a need for dose escalation, or surgery. Clinical response was defined as treatment continuation in the absence of any of the aforementioned failure criteria. Results: Sixty patients with CD receiving IFX therapy were included in the study. The patients were followed for a median of 16 months (5-24 months) after an index intestinal ultrasound. Thirty-eight patients (63.3%) maintained response to the therapy and 22 patients (36.6%) failed the treatment, with a mean follow up of 10.5 months (6.5-17 months) vs 9.25 months (1-10.25 months), respectively. On univariate analysis, the only variables differing between treatment response and failure were a TI thickness of 2.8 vs 5 mm (P 0.0001) and an IFX trough level of 6.6 vs 3.9 ug/mL (P = 0.008). On multivariable analysis, only a small bowel thickness of 4 mm was associated with the risk of treatment failure (odds ratio, 2.9; 95% CI, 1.49-5.55; P = 0.002). Conclusions: Our findings suggest that transmural thickness of 4 mm can predict subsequent treatment failure in patients with CD treated using IFX, indicating transmural thickness 4 mm as a potential novel valuable therapeutic target.
KW - Crohn disease
KW - bowel wall thickness
KW - infliximab
KW - intestinal ultrasound
KW - treatment response
UR - http://www.scopus.com/inward/record.url?scp=85091324772&partnerID=8YFLogxK
U2 - 10.1093/ibd/izaa219
DO - 10.1093/ibd/izaa219
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C2 - 32860057
AN - SCOPUS:85091324772
SN - 1078-0998
VL - 26
SP - 1619
EP - 1625
JO - Inflammatory Bowel Diseases
JF - Inflammatory Bowel Diseases
IS - 10
ER -