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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...

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Autores principales: You, Hai-zhen, Zhang, Jie, Du, Yaning, Yu, Ping-bo, Li, Lei, Xie, Jing, Mi, Yunhui, Hou, Zhaoyuan, Yang, Xiao-Dong, Sun, Ke-Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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.
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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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