AI Article Synopsis

  • Anti-tumor necrosis factor (TNF) -α antibodies, such as adalimumab (ADA), play a key role in treating ulcerative colitis (UC), and this study examines serum albumin (Alb) levels as a potential predictor of ADA treatment success.
  • In a study with 34 UC patients treated with ADA, those who experienced treatment failure within six months had a significantly lower Alb ratio at week 2 compared to those who did not fail.
  • The study found a week 2/week 0 Alb ratio cut-off of 1.00 effectively predicts treatment failure, with a high area under the ROC curve (0.868), indicating a strong correlation between Alb levels and ADA effectiveness.

Article Abstract

Anti-tumor necrosis factor (TNF) -α antibodies, including infliximab (IFX), adalimumab (ADA), and golimumab, which were the first biologic therapeutic agents, have a crucial position in advanced therapy for ulcerative colitis (UC). We aimed to investigate serum albumin (Alb) change as a prognostic factor for the therapeutic effect of ADA in UC. Thirty-four patients with UC treated with ADA were enrolled in this study and were divided into failure and non-failure groups. Biological data, such as Alb were compared between the two groups. Thirteen patients showed failure within six months. Examination of the biological data showed a significant difference between the two groups only in the week 2/week 0 Alb ratio. In receiver-operating characteristic (ROC) curve analysis to predict failure, the cut-off value of week 2/week 0 Alb ratio was 1.00, and the area under the curve was 0.868 (95% confidence interval: 0.738-0.999). In addition, in the sub-group analysis of only clinically active patients, the week 2/week 0 Alb ratio of the non-failure group was significantly higher than that of the failure group, and the cut-off-value in ROC analysis was 1.00. Week 2/week 0 Alb ratio ≤ 1 predicts failure within six months of ADA for UC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10760906PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0295681PLOS

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