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Association of serum biomarkers with early neurologic improvement after intravenous thrombolysis in ischemic stroke

BACKGROUND: Early neurologic improvement (ENI) after intravenous thrombolysis is associated with favorable outcome, but associated serum biomarkers were not fully determined. We aimed to investigate the issue based on a prospective cohort. METHODS: In INTRECIS study, five centers were designed to co...

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Autores principales: Cui, Yu, Wang, Xin-Hong, Zhao, Yong, Chen, Shao-Yuan, Sheng, Bao-Ying, Wang, Li-Hua, Chen, Hui-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9621449/
https://www.ncbi.nlm.nih.gov/pubmed/36315566
http://dx.doi.org/10.1371/journal.pone.0277020
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author Cui, Yu
Wang, Xin-Hong
Zhao, Yong
Chen, Shao-Yuan
Sheng, Bao-Ying
Wang, Li-Hua
Chen, Hui-Sheng
author_facet Cui, Yu
Wang, Xin-Hong
Zhao, Yong
Chen, Shao-Yuan
Sheng, Bao-Ying
Wang, Li-Hua
Chen, Hui-Sheng
author_sort Cui, Yu
collection PubMed
description BACKGROUND: Early neurologic improvement (ENI) after intravenous thrombolysis is associated with favorable outcome, but associated serum biomarkers were not fully determined. We aimed to investigate the issue based on a prospective cohort. METHODS: In INTRECIS study, five centers were designed to consecutively collect blood sample from enrolled patients. The patients with ENI and without ENI were matched by propensity score matching with a ratio of 1:1. Preset 49 biomarkers were measured through microarray analysis. Enrichment of gene ontology and pathway, and protein-protein interaction network were analyzed in the identified biomarkers. RESULTS: Of 358 patients, 19 patients with ENI were assigned to ENI group, while 19 matched patients without ENI were assigned to Non ENI group. A total of nine biomarkers were found different between two groups, in which serum levels of chemokine (C-C motif) ligand (CCL)-23, chemokine (C-X-C motif) ligand (CXCL)-12, insulin-like growth factor binding protein (IGFBP)-6, interleukin (IL)-5, lymphatic vessel endothelial hyaluronan receptor (LYVE)-1, plasminogen activator inhibitor (PAI)-1, platelet-derived growth factor (PDGF)-AA, suppression of tumorigenicity (ST)-2, and tumor necrosis factor (TNF)-α were higher in the ENI group, compared with those in the Non ENI group. CONCLUSIONS: We found that serum levels of CCL-23, CXCL-12, IGFBP-6, IL-5, LYVE-1, PAI-1, PDGF-AA, ST-2, and TNF-α at admission were associated with post-thrombolytic ENI in stroke. The role of biomarkers warrants further investigation. TRIAL REGISTRATION: Clinical Trial Registration: https://www.clinicaltrials.gov; identifier: NCT02854592.
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spelling pubmed-96214492022-11-01 Association of serum biomarkers with early neurologic improvement after intravenous thrombolysis in ischemic stroke Cui, Yu Wang, Xin-Hong Zhao, Yong Chen, Shao-Yuan Sheng, Bao-Ying Wang, Li-Hua Chen, Hui-Sheng PLoS One Research Article BACKGROUND: Early neurologic improvement (ENI) after intravenous thrombolysis is associated with favorable outcome, but associated serum biomarkers were not fully determined. We aimed to investigate the issue based on a prospective cohort. METHODS: In INTRECIS study, five centers were designed to consecutively collect blood sample from enrolled patients. The patients with ENI and without ENI were matched by propensity score matching with a ratio of 1:1. Preset 49 biomarkers were measured through microarray analysis. Enrichment of gene ontology and pathway, and protein-protein interaction network were analyzed in the identified biomarkers. RESULTS: Of 358 patients, 19 patients with ENI were assigned to ENI group, while 19 matched patients without ENI were assigned to Non ENI group. A total of nine biomarkers were found different between two groups, in which serum levels of chemokine (C-C motif) ligand (CCL)-23, chemokine (C-X-C motif) ligand (CXCL)-12, insulin-like growth factor binding protein (IGFBP)-6, interleukin (IL)-5, lymphatic vessel endothelial hyaluronan receptor (LYVE)-1, plasminogen activator inhibitor (PAI)-1, platelet-derived growth factor (PDGF)-AA, suppression of tumorigenicity (ST)-2, and tumor necrosis factor (TNF)-α were higher in the ENI group, compared with those in the Non ENI group. CONCLUSIONS: We found that serum levels of CCL-23, CXCL-12, IGFBP-6, IL-5, LYVE-1, PAI-1, PDGF-AA, ST-2, and TNF-α at admission were associated with post-thrombolytic ENI in stroke. The role of biomarkers warrants further investigation. TRIAL REGISTRATION: Clinical Trial Registration: https://www.clinicaltrials.gov; identifier: NCT02854592. Public Library of Science 2022-10-31 /pmc/articles/PMC9621449/ /pubmed/36315566 http://dx.doi.org/10.1371/journal.pone.0277020 Text en © 2022 Cui et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Cui, Yu
Wang, Xin-Hong
Zhao, Yong
Chen, Shao-Yuan
Sheng, Bao-Ying
Wang, Li-Hua
Chen, Hui-Sheng
Association of serum biomarkers with early neurologic improvement after intravenous thrombolysis in ischemic stroke
title Association of serum biomarkers with early neurologic improvement after intravenous thrombolysis in ischemic stroke
title_full Association of serum biomarkers with early neurologic improvement after intravenous thrombolysis in ischemic stroke
title_fullStr Association of serum biomarkers with early neurologic improvement after intravenous thrombolysis in ischemic stroke
title_full_unstemmed Association of serum biomarkers with early neurologic improvement after intravenous thrombolysis in ischemic stroke
title_short Association of serum biomarkers with early neurologic improvement after intravenous thrombolysis in ischemic stroke
title_sort association of serum biomarkers with early neurologic improvement after intravenous thrombolysis in ischemic stroke
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9621449/
https://www.ncbi.nlm.nih.gov/pubmed/36315566
http://dx.doi.org/10.1371/journal.pone.0277020
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