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Peripheral blood neurotrophic factor levels in children with autism spectrum disorder: a meta-analysis

Increasing evidence suggests that abnormal regulation of neurotrophic factors is involved in the etiology and pathogenesis of Autism Spectrum Disorder (ASD). However, clinical data on neurotrophic factor levels in children with ASD were inconsistent. Therefore, we performed a systematic review of pe...

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Autores principales: Liu, Shu-Han, Shi, Xiao-Jie, Fan, Fang-Cheng, Cheng, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794512/
https://www.ncbi.nlm.nih.gov/pubmed/33420109
http://dx.doi.org/10.1038/s41598-020-79080-w
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author Liu, Shu-Han
Shi, Xiao-Jie
Fan, Fang-Cheng
Cheng, Yong
author_facet Liu, Shu-Han
Shi, Xiao-Jie
Fan, Fang-Cheng
Cheng, Yong
author_sort Liu, Shu-Han
collection PubMed
description Increasing evidence suggests that abnormal regulation of neurotrophic factors is involved in the etiology and pathogenesis of Autism Spectrum Disorder (ASD). However, clinical data on neurotrophic factor levels in children with ASD were inconsistent. Therefore, we performed a systematic review of peripheral blood neurotrophic factors levels in children with ASD, and quantitatively summarized the clinical data of peripheral blood neurotrophic factors in ASD children and healthy controls. A systematic search of PubMed and Web of Science identified 31 studies with 2627 ASD children and 4418 healthy controls to be included in the meta-analysis. The results of random effect meta-analysis showed that the peripheral blood levels of brain-derived neurotrophic factor (Hedges’ g = 0.302; 95% CI = 0.014 to 0.591; P = 0.040) , nerve growth factor (Hedges’ g = 0.395; 95% CI = 0.104 to 0.686; P = 0.008) and vascular endothelial growth factor (VEGF) (Hedges’ g = 0.097; 95% CI = 0.018 to 0.175; P = 0.016) in children with ASD were significantly higher than that of healthy controls, whereas blood neurotrophin-3 (Hedges’ g =  − 0.795; 95% CI =  − 1.723 to 0.134; P = 0.093) and neurotrophin-4 (Hedges’ g = 0.182; 95% CI =  − 0.285 to 0.650; P = 0.445) levels did not show significant differences between cases and controls. Taken together, these results clarified circulating neurotrophic factor profile in children with ASD, strengthening clinical evidence of neurotrophic factor aberrations in children with ASD.
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spelling pubmed-77945122021-01-12 Peripheral blood neurotrophic factor levels in children with autism spectrum disorder: a meta-analysis Liu, Shu-Han Shi, Xiao-Jie Fan, Fang-Cheng Cheng, Yong Sci Rep Article Increasing evidence suggests that abnormal regulation of neurotrophic factors is involved in the etiology and pathogenesis of Autism Spectrum Disorder (ASD). However, clinical data on neurotrophic factor levels in children with ASD were inconsistent. Therefore, we performed a systematic review of peripheral blood neurotrophic factors levels in children with ASD, and quantitatively summarized the clinical data of peripheral blood neurotrophic factors in ASD children and healthy controls. A systematic search of PubMed and Web of Science identified 31 studies with 2627 ASD children and 4418 healthy controls to be included in the meta-analysis. The results of random effect meta-analysis showed that the peripheral blood levels of brain-derived neurotrophic factor (Hedges’ g = 0.302; 95% CI = 0.014 to 0.591; P = 0.040) , nerve growth factor (Hedges’ g = 0.395; 95% CI = 0.104 to 0.686; P = 0.008) and vascular endothelial growth factor (VEGF) (Hedges’ g = 0.097; 95% CI = 0.018 to 0.175; P = 0.016) in children with ASD were significantly higher than that of healthy controls, whereas blood neurotrophin-3 (Hedges’ g =  − 0.795; 95% CI =  − 1.723 to 0.134; P = 0.093) and neurotrophin-4 (Hedges’ g = 0.182; 95% CI =  − 0.285 to 0.650; P = 0.445) levels did not show significant differences between cases and controls. Taken together, these results clarified circulating neurotrophic factor profile in children with ASD, strengthening clinical evidence of neurotrophic factor aberrations in children with ASD. Nature Publishing Group UK 2021-01-08 /pmc/articles/PMC7794512/ /pubmed/33420109 http://dx.doi.org/10.1038/s41598-020-79080-w Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Shu-Han
Shi, Xiao-Jie
Fan, Fang-Cheng
Cheng, Yong
Peripheral blood neurotrophic factor levels in children with autism spectrum disorder: a meta-analysis
title Peripheral blood neurotrophic factor levels in children with autism spectrum disorder: a meta-analysis
title_full Peripheral blood neurotrophic factor levels in children with autism spectrum disorder: a meta-analysis
title_fullStr Peripheral blood neurotrophic factor levels in children with autism spectrum disorder: a meta-analysis
title_full_unstemmed Peripheral blood neurotrophic factor levels in children with autism spectrum disorder: a meta-analysis
title_short Peripheral blood neurotrophic factor levels in children with autism spectrum disorder: a meta-analysis
title_sort peripheral blood neurotrophic factor levels in children with autism spectrum disorder: a meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794512/
https://www.ncbi.nlm.nih.gov/pubmed/33420109
http://dx.doi.org/10.1038/s41598-020-79080-w
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