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Effect of obesity on vedolizumab response in inflammatory bowel disease
BACKGROUND: Vedolizumab is used in inflammatory bowel disease (IBD), administered as a non-weight-based fixed dose. A higher body mass index (BMI) is associated with lower serum vedolizumab levels, but it is unclear whether it is associated with an unfavorable response to vedolizumab. We examined th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hellenic Society of Gastroenterology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062841/ https://www.ncbi.nlm.nih.gov/pubmed/35599926 http://dx.doi.org/10.20524/aog.2022.0699 |
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author | Levine, Louis J. Gaidos, Jill K. J. Proctor, Deborah D. Viana, Artur V. Al-Bawardy, Badr |
author_facet | Levine, Louis J. Gaidos, Jill K. J. Proctor, Deborah D. Viana, Artur V. Al-Bawardy, Badr |
author_sort | Levine, Louis J. |
collection | PubMed |
description | BACKGROUND: Vedolizumab is used in inflammatory bowel disease (IBD), administered as a non-weight-based fixed dose. A higher body mass index (BMI) is associated with lower serum vedolizumab levels, but it is unclear whether it is associated with an unfavorable response to vedolizumab. We examined the relationship between BMI and the need for dose escalation, and the overall response to vedolizumab in IBD patients. METHODS: This was a single-center, retrospective study of IBD patients who received vedolizumab between 1(st) July 2014 and 1(st) September 2020. The primary outcome was need for vedolizumab dose escalation or discontinuation. Secondary outcomes were steroid-free clinical remission (SFCR), endoscopic remission, and normal serum C-reactive protein (CRP). Outcomes were compared between patients with BMI <30 kg/m(2) (non-obese) or ≥30 kg/m(>2) (obese). RESULTS: 190 patients were included, with a median follow-up time of 21 months. Median age was 37 years, 50.5% were male, and median BMI was 24.8 kg/m(2) (75.3% of patients had BMI <30 kg/m(2)). Vedolizumab was dose-escalated in 48.9% of the obese group vs. 42% of the non-obese group (P=0.4). Vedolizumab was discontinued in 31.9% of the obese group vs. 53.2% of the non-obese group (P=0.01). The rate of CRP normalization was significantly lower in the obese group (46.2% vs. 66%, P=0.03). SFCR and endoscopic remission rates were not significantly different between the groups. CONCLUSIONS: Obesity was not associated with higher rates of vedolizumab dose escalation. However, it was associated with lower rates of vedolizumab discontinuation and CRP normalization, but not SFCR or endoscopic remission. |
format | Online Article Text |
id | pubmed-9062841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hellenic Society of Gastroenterology |
record_format | MEDLINE/PubMed |
spelling | pubmed-90628412022-05-19 Effect of obesity on vedolizumab response in inflammatory bowel disease Levine, Louis J. Gaidos, Jill K. J. Proctor, Deborah D. Viana, Artur V. Al-Bawardy, Badr Ann Gastroenterol Original Article BACKGROUND: Vedolizumab is used in inflammatory bowel disease (IBD), administered as a non-weight-based fixed dose. A higher body mass index (BMI) is associated with lower serum vedolizumab levels, but it is unclear whether it is associated with an unfavorable response to vedolizumab. We examined the relationship between BMI and the need for dose escalation, and the overall response to vedolizumab in IBD patients. METHODS: This was a single-center, retrospective study of IBD patients who received vedolizumab between 1(st) July 2014 and 1(st) September 2020. The primary outcome was need for vedolizumab dose escalation or discontinuation. Secondary outcomes were steroid-free clinical remission (SFCR), endoscopic remission, and normal serum C-reactive protein (CRP). Outcomes were compared between patients with BMI <30 kg/m(2) (non-obese) or ≥30 kg/m(>2) (obese). RESULTS: 190 patients were included, with a median follow-up time of 21 months. Median age was 37 years, 50.5% were male, and median BMI was 24.8 kg/m(2) (75.3% of patients had BMI <30 kg/m(2)). Vedolizumab was dose-escalated in 48.9% of the obese group vs. 42% of the non-obese group (P=0.4). Vedolizumab was discontinued in 31.9% of the obese group vs. 53.2% of the non-obese group (P=0.01). The rate of CRP normalization was significantly lower in the obese group (46.2% vs. 66%, P=0.03). SFCR and endoscopic remission rates were not significantly different between the groups. CONCLUSIONS: Obesity was not associated with higher rates of vedolizumab dose escalation. However, it was associated with lower rates of vedolizumab discontinuation and CRP normalization, but not SFCR or endoscopic remission. Hellenic Society of Gastroenterology 2022 2022-02-21 /pmc/articles/PMC9062841/ /pubmed/35599926 http://dx.doi.org/10.20524/aog.2022.0699 Text en Copyright: © Hellenic Society of Gastroenterology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Levine, Louis J. Gaidos, Jill K. J. Proctor, Deborah D. Viana, Artur V. Al-Bawardy, Badr Effect of obesity on vedolizumab response in inflammatory bowel disease |
title | Effect of obesity on vedolizumab response in inflammatory bowel disease |
title_full | Effect of obesity on vedolizumab response in inflammatory bowel disease |
title_fullStr | Effect of obesity on vedolizumab response in inflammatory bowel disease |
title_full_unstemmed | Effect of obesity on vedolizumab response in inflammatory bowel disease |
title_short | Effect of obesity on vedolizumab response in inflammatory bowel disease |
title_sort | effect of obesity on vedolizumab response in inflammatory bowel disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062841/ https://www.ncbi.nlm.nih.gov/pubmed/35599926 http://dx.doi.org/10.20524/aog.2022.0699 |
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