TY - JOUR
T1 - BMI is important in predicting the loss of response in inflammatory bowel disease patients on tumour necrosis factor- inhibitors
AU - Chuck, Winnie
AU - Shadbolt, Bruce Frederick
AU - Nordin, Fariza
AU - Subramaniam, Kavitha
N1 - Publisher Copyright:
© 2022 Lippincott Williams and Wilkins. All rights reserved.
PY - 2022/6/1
Y1 - 2022/6/1
N2 - Introduction Obesity is an emerging phenomenon among patients with inflammatory bowel disease (IBD). This study aims to evaluate whether the response to tumour necrosis factor- (TNF-) inhibitors (infliximab and adalimumab) could be influenced by BMI in IBD. Methods We identified a cohort of 181 IBD patients attending a single-tertiary centre, naive to biologic therapy and stratified them according to their BMI. The primary outcome is the first occurrence of loss of response (LOR). Results The median BMI was 26 kg/m2(15-63 kg/m2). Approximately 68% of patients had LOR on both adalimumab (ADA) (n = 52) and infliximab (IFX) (n = 71). However, 83% on ADA with BMI ≥30 kg/m2had LOR compared to 61% on IFX with BMI ≥30 kg/m2. For patients on ADA, Cox regression analysis revealed that after accounting for age, sex, disease type, duration of disease, fistulising disease, smoking status, haemoglobin, C-reactive protein, albumin and platelet levels, there were statistically significant associations between BMI (≥30 kg/m2vs. <30 kg/m2) and LOR [P = 0.010; hazard ratio (HR) 3.2; confidence interval (CI), 1.3-7.6]. However, for patients on IFX, after accounting for the same factors, the only significant factor was the association of lower rate of LOR with higher albumin levels (P = 0.024; HR 0.95; CI, 0.91-0.99). There was an increased accelerated time to LOR for patients on ADA with BMI ≥30 kg/m2compared to BMI <30 kg/m2(P = 0.026). However, there was no difference in time to LOR for patients on IFX (P = 0.177). Conclusion BMI is important in predicting the LOR among IBD patients on TNF- inhibitors, especially among patients receiving ADA.
AB - Introduction Obesity is an emerging phenomenon among patients with inflammatory bowel disease (IBD). This study aims to evaluate whether the response to tumour necrosis factor- (TNF-) inhibitors (infliximab and adalimumab) could be influenced by BMI in IBD. Methods We identified a cohort of 181 IBD patients attending a single-tertiary centre, naive to biologic therapy and stratified them according to their BMI. The primary outcome is the first occurrence of loss of response (LOR). Results The median BMI was 26 kg/m2(15-63 kg/m2). Approximately 68% of patients had LOR on both adalimumab (ADA) (n = 52) and infliximab (IFX) (n = 71). However, 83% on ADA with BMI ≥30 kg/m2had LOR compared to 61% on IFX with BMI ≥30 kg/m2. For patients on ADA, Cox regression analysis revealed that after accounting for age, sex, disease type, duration of disease, fistulising disease, smoking status, haemoglobin, C-reactive protein, albumin and platelet levels, there were statistically significant associations between BMI (≥30 kg/m2vs. <30 kg/m2) and LOR [P = 0.010; hazard ratio (HR) 3.2; confidence interval (CI), 1.3-7.6]. However, for patients on IFX, after accounting for the same factors, the only significant factor was the association of lower rate of LOR with higher albumin levels (P = 0.024; HR 0.95; CI, 0.91-0.99). There was an increased accelerated time to LOR for patients on ADA with BMI ≥30 kg/m2compared to BMI <30 kg/m2(P = 0.026). However, there was no difference in time to LOR for patients on IFX (P = 0.177). Conclusion BMI is important in predicting the LOR among IBD patients on TNF- inhibitors, especially among patients receiving ADA.
KW - Crohn's disease
KW - inflammatory bowel disease
KW - obesity
KW - tumour necrosis factor- inhibitors
KW - ulcerative colitis
UR - http://www.scopus.com/inward/record.url?scp=85129779464&partnerID=8YFLogxK
U2 - 10.1097/MEG.0000000000002371
DO - 10.1097/MEG.0000000000002371
M3 - Article
SN - 0954-691X
VL - 34
SP - 622
EP - 629
JO - European Journal of Gastroenterology and Hepatology
JF - European Journal of Gastroenterology and Hepatology
IS - 6
ER -