Effect of Overweight and Obesity on the Response to Anti-TNF Therapy and Disease Course in Children With IBD

超重 医学 炎症性肠病 肥胖 肿瘤坏死因子α 疾病 内科学 免疫学 胃肠病学
作者
Sara Sila,M Aloi,U Cucinotta,Laura Gianolio,Maya Granot,Ondřej Hradský,Séamus Hussey,Ben Kang,Anna Karoliny,Kaija‐Leena Kolho,Jan de Laffolie,Sara Lega,Manar Matar,Lorenzo Norsa,Sharon Omiwole,Esther Orlanski‐Meyer,Laura Palomino,Pejman Rohani,Luca Scarallo,Margaret Sladek
出处
期刊:Inflammatory Bowel Diseases [Oxford University Press]
卷期号:31 (5): 1263-1271 被引量:3
标识
DOI:10.1093/ibd/izae165
摘要

Abstract Background This study aimed to evaluate the effect of overweight and obesity at the start of anti-TNF therapy on treatment response and relapse rate in children with inflammatory bowel disease (IBD). Methods This multicenter, retrospective cohort study included 22 IBD centers in 14 countries. Children diagnosed with IBD in whom antitumor necrosis factor (anti-TNF) was introduced were included; those who were overweight/obese were compared with children who were well/undernourished. Results Six hundred thirty-seven children (370 [58%] males; mean age 11.5 ± 3.5 years) were included; 140 (22%) were in the overweight/obese group (OG) and 497 (78%) had BMI ≤1 SD (CG). The mean follow-up time was 141 ± 78 weeks (median 117 weeks). There was no difference in the loss of response (LOR) to anti-TNF between groups throughout the follow-up. However, children in OG had more dose escalations than controls. Male sex and lack of concomitant immunomodulators at the start of anti-TNF were risk factors associated with the LOR. There was no difference in the relapse rate in the first year after anti-TNF introduction; however, at the end of the follow-up, the relapse rate was significantly higher in the OG compared with CG (89 [64%] vs 218 [44%], respectively, P < .001). Univariate and multivariate analysis revealed that being overweight/obese, having UC, or being of male sex were factors associated with a higher risk for relapse. Conclusions Overweight/obese children with IBD were not at a higher risk of LOR to anti-TNF. Relapse in the first year after anti-TNF was introduced, but risk for relapse was increased at the end of follow-up.
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