Albumin change predicts failure in ulcerative colitis treated with adalimumab
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 f...
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Published in | PloS one Vol. 19; no. 1; p. e0295681 |
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Main Authors | , , , , , , , , , , |
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02.01.2024
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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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AbstractList | 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. Anti-tumor necrosis factor (TNF) -[alpha] 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 [less than or equal to] 1 predicts failure within six months of ADA for UC. |
Audience | Academic |
Author | Sugimoto, Ken Ishida, Natsuki Tani, Shinya Miyazu, Takahiro Iwaizumi, Moriya Hamaya, Yasushi Osawa, Satoshi Asai, Yusuke Tamura, Satoshi Takahashi, Kenichi Yamade, Mihoko |
AuthorAffiliation | 2 First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan 1 Department of Endoscopic and Photodynamic Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan 3 Department of Laboratory Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan Kurume University School of Medicine, JAPAN |
AuthorAffiliation_xml | – name: 2 First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – name: 3 Department of Laboratory Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – name: Kurume University School of Medicine, JAPAN – name: 1 Department of Endoscopic and Photodynamic Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan |
Author_xml | – sequence: 1 givenname: Natsuki surname: Ishida fullname: Ishida, Natsuki organization: Department of Endoscopic and Photodynamic Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – sequence: 2 givenname: Kenichi surname: Takahashi fullname: Takahashi, Kenichi organization: First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – sequence: 3 givenname: Yusuke surname: Asai fullname: Asai, Yusuke organization: First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – sequence: 4 givenname: Takahiro surname: Miyazu fullname: Miyazu, Takahiro organization: First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – sequence: 5 givenname: Satoshi surname: Tamura fullname: Tamura, Satoshi organization: First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – sequence: 6 givenname: Shinya surname: Tani fullname: Tani, Shinya organization: First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – sequence: 7 givenname: Mihoko surname: Yamade fullname: Yamade, Mihoko organization: First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – sequence: 8 givenname: Moriya surname: Iwaizumi fullname: Iwaizumi, Moriya organization: Department of Laboratory Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – sequence: 9 givenname: Yasushi surname: Hamaya fullname: Hamaya, Yasushi organization: First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – sequence: 10 givenname: Satoshi surname: Osawa fullname: Osawa, Satoshi organization: Department of Endoscopic and Photodynamic Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan – sequence: 11 givenname: Ken orcidid: 0000-0001-9586-1097 surname: Sugimoto fullname: Sugimoto, Ken organization: First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan |
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Copyright | Copyright: © 2024 Ishida et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. COPYRIGHT 2024 Public Library of Science 2024 Ishida et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2024 Ishida et al 2024 Ishida et al 2024 Ishida et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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SubjectTerms | Adalimumab Adalimumab - therapeutic use Albumin Analysis Antibodies Biological products Biology and Life Sciences Colitis, Ulcerative - drug therapy Colitis, Ulcerative - pathology Dosage and administration Drug therapy Endoscopy Failure Health aspects Hospitals Humans Inflammatory bowel disease Infliximab Measurement Medical colleges Medical prognosis Medicine and Health Sciences Monoclonal antibodies Patient compliance Patient outcomes Patients Pharmacology Prognosis Remission (Medicine) Retrospective Studies Serum Albumin Treatment Failure Treatment Outcome Tumor necrosis factor Tumor necrosis factor-TNF Tumor necrosis factor-α Ulcerative colitis |
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Title | Albumin change predicts failure in ulcerative colitis treated with adalimumab |
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