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A novel role of the splenic volume in Crohn’s disease: evaluating the efficacy of infliximab

Background: A number of patients with Crohn’s disease (CD) suffer from loss of response to infliximab (IFX) therapy. Splenic volume is reported to be enlarged in patients with CD compared to normal individuals. The association between splenic volume and IFX efficacy in CD remains unclear. Methods: W...

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Autores principales: Shi, Xuan, Wang, Jia-Hui, Rao, Sheng-Xiang, Liu, Tao-Tao, Wu, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470019/
https://www.ncbi.nlm.nih.gov/pubmed/37663264
http://dx.doi.org/10.3389/fphar.2023.1246657
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author Shi, Xuan
Wang, Jia-Hui
Rao, Sheng-Xiang
Liu, Tao-Tao
Wu, Hao
author_facet Shi, Xuan
Wang, Jia-Hui
Rao, Sheng-Xiang
Liu, Tao-Tao
Wu, Hao
author_sort Shi, Xuan
collection PubMed
description Background: A number of patients with Crohn’s disease (CD) suffer from loss of response to infliximab (IFX) therapy. Splenic volume is reported to be enlarged in patients with CD compared to normal individuals. The association between splenic volume and IFX efficacy in CD remains unclear. Methods: We performed a retrospective study of patients with CD who received regular IFX treatment at Zhongshan Hospital, Fudan University, between August 2015 and December 2021. We collected baseline characteristics and clinical features from medical records in the CD database of Zhongshan Hospital. We accurately measured the splenic volume using semi-auto spleen segmentation software, followed by the analysis of splenic volume and IFX efficacy. Results: We included 49 patients with CD receiving IFX treatment, of whom 41 responded to IFX and 8 failed to respond to IFX. Splenic volume, as well as volume adjusted for body mass index (SV/BMI) and body weight (SV/W), was significantly decreased after IFX treatment in responders but increased in non-responders compared to the volume before the treatment. Accordingly, the levels of leukocyte count, platelet count, C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR) were decreased after IFX treatment in responders. Contrarily, the levels of hemoglobin, albumin, and tumor necrosis factor (TNF)-α were elevated in responders. Moreover, both CRP and TNF-α levels were significantly positively correlated with SV/BMI in all patients. Conclusion: Splenic volume, especially SV/BMI and SV/W, was reduced after IFX treatment in CD patients responsive to IFX. SV/BMI was positively correlated with disease activity. Splenic volume is a promising indicator to evaluate IFX efficacy in CD.
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spelling pubmed-104700192023-09-01 A novel role of the splenic volume in Crohn’s disease: evaluating the efficacy of infliximab Shi, Xuan Wang, Jia-Hui Rao, Sheng-Xiang Liu, Tao-Tao Wu, Hao Front Pharmacol Pharmacology Background: A number of patients with Crohn’s disease (CD) suffer from loss of response to infliximab (IFX) therapy. Splenic volume is reported to be enlarged in patients with CD compared to normal individuals. The association between splenic volume and IFX efficacy in CD remains unclear. Methods: We performed a retrospective study of patients with CD who received regular IFX treatment at Zhongshan Hospital, Fudan University, between August 2015 and December 2021. We collected baseline characteristics and clinical features from medical records in the CD database of Zhongshan Hospital. We accurately measured the splenic volume using semi-auto spleen segmentation software, followed by the analysis of splenic volume and IFX efficacy. Results: We included 49 patients with CD receiving IFX treatment, of whom 41 responded to IFX and 8 failed to respond to IFX. Splenic volume, as well as volume adjusted for body mass index (SV/BMI) and body weight (SV/W), was significantly decreased after IFX treatment in responders but increased in non-responders compared to the volume before the treatment. Accordingly, the levels of leukocyte count, platelet count, C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR) were decreased after IFX treatment in responders. Contrarily, the levels of hemoglobin, albumin, and tumor necrosis factor (TNF)-α were elevated in responders. Moreover, both CRP and TNF-α levels were significantly positively correlated with SV/BMI in all patients. Conclusion: Splenic volume, especially SV/BMI and SV/W, was reduced after IFX treatment in CD patients responsive to IFX. SV/BMI was positively correlated with disease activity. Splenic volume is a promising indicator to evaluate IFX efficacy in CD. Frontiers Media S.A. 2023-08-17 /pmc/articles/PMC10470019/ /pubmed/37663264 http://dx.doi.org/10.3389/fphar.2023.1246657 Text en Copyright © 2023 Shi, Wang, Rao, Liu and Wu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Shi, Xuan
Wang, Jia-Hui
Rao, Sheng-Xiang
Liu, Tao-Tao
Wu, Hao
A novel role of the splenic volume in Crohn’s disease: evaluating the efficacy of infliximab
title A novel role of the splenic volume in Crohn’s disease: evaluating the efficacy of infliximab
title_full A novel role of the splenic volume in Crohn’s disease: evaluating the efficacy of infliximab
title_fullStr A novel role of the splenic volume in Crohn’s disease: evaluating the efficacy of infliximab
title_full_unstemmed A novel role of the splenic volume in Crohn’s disease: evaluating the efficacy of infliximab
title_short A novel role of the splenic volume in Crohn’s disease: evaluating the efficacy of infliximab
title_sort novel role of the splenic volume in crohn’s disease: evaluating the efficacy of infliximab
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470019/
https://www.ncbi.nlm.nih.gov/pubmed/37663264
http://dx.doi.org/10.3389/fphar.2023.1246657
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