AI Article Synopsis

  • Adalimumab (ADA) levels and the presence of anti-ADA antibodies (AAA) significantly impact mucosal healing in patients with inflammatory bowel disease (IBD), and this study aimed to clarify their correlation with clinical outcomes in a real-world setting.
  • Conducted at a single center, the study focused on 52 patients (19 with ulcerative colitis and 33 with Crohn's disease) who were monitored for ADA and AAA levels after treatment from 2007 to 2018, revealing a 23.1% AAA positivity rate.
  • Key findings included that higher serum ADA levels were linked to better remission outcomes, suggesting a cutoff of 11.1 μg/mL for endoscopic remission and emphasizing

Article Abstract

Adalimumab (ADA) trough level and anti-ADA antibody (AAA) positivity influence mucosal healing and loss of response in patients with inflammatory bowel disease (IBD). In this study, we clarified the correlation between ADA monitoring, including non-trough level, and real-world IBD clinical outcomes. This retrospective, observational, single-center study involved patients with ulcerative colitis (19) and Crohn's disease (33) treated with ADA from January 2007 to August 2018. Serum ADA and AAA levels were measured 4‒14 days after ADA administration. The AAA positivity rate was 23.1% (12/52). ADA continuity was higher in AAA-negative patients than in AAA-positive patients (P = 0.223). Receiver operating characteristic (ROC) analysis revealed that a serum AAA cut-off of 9.2 μg/mL was associated with ADA continuity. The ADA level was significantly higher in the endoscopic remission group than in the non-remission group (P = 0.02). Based on the ROC curve analysis results of serum ADA level and endoscopic remission, the cut-off value of the serum ADA level was set to 11.1 μg/mL. Under the combined use of ADA with immunomodulators and AAA positivity, ADA continuity was significantly higher when the serum AAA level at 4-14 days after ADA administration was ≥9.2 μg/mL. Furthermore, endoscopic remission can be expected with a serum ADA level of ≥11.1 μg/mL. Overall, to predict clinical outcomes, it would be useful to measure the blood level of ADA regardless of the timing of the trough.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270420PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0254548PLOS

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