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Association of elevated plasma CCL5 levels with high risk for tic disorders in children
Abnormal levels of some peripheral cytokines have been reported in children patients with tic disorders (TDs), but none of these cytokines can be a biomarker for this disease. Our aim was to systemically profile differentially expressed cytokines (DECs) in the blood of TD patients, examine their ass...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113459/ https://www.ncbi.nlm.nih.gov/pubmed/37090922 http://dx.doi.org/10.3389/fped.2023.1126839 |
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author | You, Hai-zhen Zhang, Jie Du, Yaning Yu, Ping-bo Li, Lei Xie, Jing Mi, Yunhui Hou, Zhaoyuan Yang, Xiao-Dong Sun, Ke-Xing |
author_facet | You, Hai-zhen Zhang, Jie Du, Yaning Yu, Ping-bo Li, Lei Xie, Jing Mi, Yunhui Hou, Zhaoyuan Yang, Xiao-Dong Sun, Ke-Xing |
author_sort | You, Hai-zhen |
collection | PubMed |
description | Abnormal levels of some peripheral cytokines have been reported in children patients with tic disorders (TDs), but none of these cytokines can be a biomarker for this disease. Our aim was to systemically profile differentially expressed cytokines (DECs) in the blood of TD patients, examine their associations with TD development, and identify from them potential biomarkers for the prediction and management of the risk for TDs. In this study, a cytokine array capable of measuring 105 cytokines was used to screen for DECs in the plasma from 53 comorbidity-free and drug-naïve TD patients and 37 age-matched healthy controls. DECs were verified by ELISA and their associations with TD development were evaluated by binary logistic regression analysis. Elevation of a set of cytokines was observed in TD patients compared with controls, including previously uncharacterized cytokines in tic disorders, CCL5, Serpin E1, Thrombospondin-1, MIF, PDGF-AA, and PDGF-AB/BB. Further analysis of DECs revealed a significant association of elevated CCL5 with TD development (p = 0.005) and a significant ROC curve for CCL5 as a risk factor [AUC, 0.801 (95% CI: 0.707–0.895), p < 0.0001]. CONCLUSION: This study identifies associations of a set of circulating cytokines, particularly CCL5 with TD development, and provides evidence that high blood CCL5 has potential to be a risk factor for TD development. CLINICAL TRIAL REGISTRATION: identifier ChiCTR-2000029616. |
format | Online Article Text |
id | pubmed-10113459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101134592023-04-20 Association of elevated plasma CCL5 levels with high risk for tic disorders in children You, Hai-zhen Zhang, Jie Du, Yaning Yu, Ping-bo Li, Lei Xie, Jing Mi, Yunhui Hou, Zhaoyuan Yang, Xiao-Dong Sun, Ke-Xing Front Pediatr Pediatrics Abnormal levels of some peripheral cytokines have been reported in children patients with tic disorders (TDs), but none of these cytokines can be a biomarker for this disease. Our aim was to systemically profile differentially expressed cytokines (DECs) in the blood of TD patients, examine their associations with TD development, and identify from them potential biomarkers for the prediction and management of the risk for TDs. In this study, a cytokine array capable of measuring 105 cytokines was used to screen for DECs in the plasma from 53 comorbidity-free and drug-naïve TD patients and 37 age-matched healthy controls. DECs were verified by ELISA and their associations with TD development were evaluated by binary logistic regression analysis. Elevation of a set of cytokines was observed in TD patients compared with controls, including previously uncharacterized cytokines in tic disorders, CCL5, Serpin E1, Thrombospondin-1, MIF, PDGF-AA, and PDGF-AB/BB. Further analysis of DECs revealed a significant association of elevated CCL5 with TD development (p = 0.005) and a significant ROC curve for CCL5 as a risk factor [AUC, 0.801 (95% CI: 0.707–0.895), p < 0.0001]. CONCLUSION: This study identifies associations of a set of circulating cytokines, particularly CCL5 with TD development, and provides evidence that high blood CCL5 has potential to be a risk factor for TD development. CLINICAL TRIAL REGISTRATION: identifier ChiCTR-2000029616. Frontiers Media S.A. 2023-04-05 /pmc/articles/PMC10113459/ /pubmed/37090922 http://dx.doi.org/10.3389/fped.2023.1126839 Text en © 2023 You, Zhang, Du, Yu, Li, Xie, Mi, Hou, Yang and Sun. 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) (https://creativecommons.org/licenses/by/4.0/) . 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 | Pediatrics You, Hai-zhen Zhang, Jie Du, Yaning Yu, Ping-bo Li, Lei Xie, Jing Mi, Yunhui Hou, Zhaoyuan Yang, Xiao-Dong Sun, Ke-Xing Association of elevated plasma CCL5 levels with high risk for tic disorders in children |
title | Association of elevated plasma CCL5 levels with high risk for tic disorders in children |
title_full | Association of elevated plasma CCL5 levels with high risk for tic disorders in children |
title_fullStr | Association of elevated plasma CCL5 levels with high risk for tic disorders in children |
title_full_unstemmed | Association of elevated plasma CCL5 levels with high risk for tic disorders in children |
title_short | Association of elevated plasma CCL5 levels with high risk for tic disorders in children |
title_sort | association of elevated plasma ccl5 levels with high risk for tic disorders in children |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113459/ https://www.ncbi.nlm.nih.gov/pubmed/37090922 http://dx.doi.org/10.3389/fped.2023.1126839 |
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