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Correlation between serum cytokines and clinicopathological features in patients with drug-induced liver injury
Objectives: Changes in serum levels of cytokines have been proposed as possible biological markers of tissue damage, including drug-induced liver injury (DILI). Here, we aimed to screen cytokine markers that have guiding significance for the degree of inflammation of DILI. Patients and methods: 54 p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773069/ https://www.ncbi.nlm.nih.gov/pubmed/36569295 http://dx.doi.org/10.3389/fphar.2022.1070802 |
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author | Zhang, Yu Gao, Hui Zhang, Yu Shao, Yue-Ming Zhang, Rui-Hua Wen, Xiao-Yu |
author_facet | Zhang, Yu Gao, Hui Zhang, Yu Shao, Yue-Ming Zhang, Rui-Hua Wen, Xiao-Yu |
author_sort | Zhang, Yu |
collection | PubMed |
description | Objectives: Changes in serum levels of cytokines have been proposed as possible biological markers of tissue damage, including drug-induced liver injury (DILI). Here, we aimed to screen cytokine markers that have guiding significance for the degree of inflammation of DILI. Patients and methods: 54 patients with DILI were retrospectively analyzed as the experimental group, and 14 healthy subjects were randomly selected as the control group. A total of 20 cytokines were detected by using a cytokine protein antibody chip, and differentially expressed proteins were screened. Results: There were significant differences in serum cytokines between DILI patients and healthy controls. Compared with the control group, the DILI group expressed 11 differential proteins. IL-8, TNF RII, TNFα, TNF RI, MIP-1β, MIP-1α, and IL-1β were differentially expressed in DILI patients with different degrees of inflammation from G1 to G4. MIG, IL-12p40, and IL-10 were differentially expressed in the higher degree of inflammation groups (G2, G3, and G4 groups). Tissue inhibitor of metalloproteinases-1 (TIMP-1) was differentially expressed in the group with the highest inflammation degree (G4 group). Chemokine C-C motif ligand 1 (I-309) was only differentially expressed in the lowest inflammation group (G1 group). Conclusion: The changes and differential expression of specific cytokine levels were helpful for evaluating different degrees of inflammation of DILI. |
format | Online Article Text |
id | pubmed-9773069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97730692022-12-23 Correlation between serum cytokines and clinicopathological features in patients with drug-induced liver injury Zhang, Yu Gao, Hui Zhang, Yu Shao, Yue-Ming Zhang, Rui-Hua Wen, Xiao-Yu Front Pharmacol Pharmacology Objectives: Changes in serum levels of cytokines have been proposed as possible biological markers of tissue damage, including drug-induced liver injury (DILI). Here, we aimed to screen cytokine markers that have guiding significance for the degree of inflammation of DILI. Patients and methods: 54 patients with DILI were retrospectively analyzed as the experimental group, and 14 healthy subjects were randomly selected as the control group. A total of 20 cytokines were detected by using a cytokine protein antibody chip, and differentially expressed proteins were screened. Results: There were significant differences in serum cytokines between DILI patients and healthy controls. Compared with the control group, the DILI group expressed 11 differential proteins. IL-8, TNF RII, TNFα, TNF RI, MIP-1β, MIP-1α, and IL-1β were differentially expressed in DILI patients with different degrees of inflammation from G1 to G4. MIG, IL-12p40, and IL-10 were differentially expressed in the higher degree of inflammation groups (G2, G3, and G4 groups). Tissue inhibitor of metalloproteinases-1 (TIMP-1) was differentially expressed in the group with the highest inflammation degree (G4 group). Chemokine C-C motif ligand 1 (I-309) was only differentially expressed in the lowest inflammation group (G1 group). Conclusion: The changes and differential expression of specific cytokine levels were helpful for evaluating different degrees of inflammation of DILI. Frontiers Media S.A. 2022-12-08 /pmc/articles/PMC9773069/ /pubmed/36569295 http://dx.doi.org/10.3389/fphar.2022.1070802 Text en Copyright © 2022 Zhang, Gao, Zhang, Shao, Zhang and Wen. 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 Zhang, Yu Gao, Hui Zhang, Yu Shao, Yue-Ming Zhang, Rui-Hua Wen, Xiao-Yu Correlation between serum cytokines and clinicopathological features in patients with drug-induced liver injury |
title | Correlation between serum cytokines and clinicopathological features in patients with drug-induced liver injury |
title_full | Correlation between serum cytokines and clinicopathological features in patients with drug-induced liver injury |
title_fullStr | Correlation between serum cytokines and clinicopathological features in patients with drug-induced liver injury |
title_full_unstemmed | Correlation between serum cytokines and clinicopathological features in patients with drug-induced liver injury |
title_short | Correlation between serum cytokines and clinicopathological features in patients with drug-induced liver injury |
title_sort | correlation between serum cytokines and clinicopathological features in patients with drug-induced liver injury |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773069/ https://www.ncbi.nlm.nih.gov/pubmed/36569295 http://dx.doi.org/10.3389/fphar.2022.1070802 |
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