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Increased peripheral blood inflammatory cytokine levels in amyotrophic lateral sclerosis: a meta-analysis study
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with poorly understood etiology. Increasing evidence suggest that inflammation may play a critical role in the pathogenesis of ALS. Several studies have demonstrated altered levels of blood cytokines in ALS, but results were in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567306/ https://www.ncbi.nlm.nih.gov/pubmed/28831083 http://dx.doi.org/10.1038/s41598-017-09097-1 |
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author | Hu, Yang Cao, Chang Qin, Xiao-Yan Yu, Yun Yuan, Jing Zhao, Yu Cheng, Yong |
author_facet | Hu, Yang Cao, Chang Qin, Xiao-Yan Yu, Yun Yuan, Jing Zhao, Yu Cheng, Yong |
author_sort | Hu, Yang |
collection | PubMed |
description | Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with poorly understood etiology. Increasing evidence suggest that inflammation may play a critical role in the pathogenesis of ALS. Several studies have demonstrated altered levels of blood cytokines in ALS, but results were inconsistent. Therefore, we did a systematic review of studies comparing blood inflammatory cytokines between ALS patients and control subjects, and quantitatively combined the clinical data with a meta-analysis. The systematic review of Pubmed and Web of Science identified 25 studies encompassing 812 ALS patients and 639 control subjects. Random-effects meta-analysis demonstrated that blood tumor necrosis factor-α (TNF; Hedges’ g = 0.655; p = 0.001), TNF receptor 1 (Hedges’ g = 0.741; p < 0.001), interleukin 6 (IL-6; Hedges’ g = 0.25; p = 0.005), IL-1β (Hedges’ g = 0.296; p = 0.038), IL-8 (Hedges’ g = 0.449; p < 0.001) and vascular endothelial growth factor (Hedges’ g = 0.891; p = 0.003) levels were significantly elevated in patients with ALS compared with control subjects. These results substantially enhance our knowledge of the inflammatory response in ALS, and peripheral blood inflammatory cytokines may be used as diagnostic biomarkers for ALS in the future. |
format | Online Article Text |
id | pubmed-5567306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55673062017-09-01 Increased peripheral blood inflammatory cytokine levels in amyotrophic lateral sclerosis: a meta-analysis study Hu, Yang Cao, Chang Qin, Xiao-Yan Yu, Yun Yuan, Jing Zhao, Yu Cheng, Yong Sci Rep Article Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with poorly understood etiology. Increasing evidence suggest that inflammation may play a critical role in the pathogenesis of ALS. Several studies have demonstrated altered levels of blood cytokines in ALS, but results were inconsistent. Therefore, we did a systematic review of studies comparing blood inflammatory cytokines between ALS patients and control subjects, and quantitatively combined the clinical data with a meta-analysis. The systematic review of Pubmed and Web of Science identified 25 studies encompassing 812 ALS patients and 639 control subjects. Random-effects meta-analysis demonstrated that blood tumor necrosis factor-α (TNF; Hedges’ g = 0.655; p = 0.001), TNF receptor 1 (Hedges’ g = 0.741; p < 0.001), interleukin 6 (IL-6; Hedges’ g = 0.25; p = 0.005), IL-1β (Hedges’ g = 0.296; p = 0.038), IL-8 (Hedges’ g = 0.449; p < 0.001) and vascular endothelial growth factor (Hedges’ g = 0.891; p = 0.003) levels were significantly elevated in patients with ALS compared with control subjects. These results substantially enhance our knowledge of the inflammatory response in ALS, and peripheral blood inflammatory cytokines may be used as diagnostic biomarkers for ALS in the future. Nature Publishing Group UK 2017-08-22 /pmc/articles/PMC5567306/ /pubmed/28831083 http://dx.doi.org/10.1038/s41598-017-09097-1 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hu, Yang Cao, Chang Qin, Xiao-Yan Yu, Yun Yuan, Jing Zhao, Yu Cheng, Yong Increased peripheral blood inflammatory cytokine levels in amyotrophic lateral sclerosis: a meta-analysis study |
title | Increased peripheral blood inflammatory cytokine levels in amyotrophic lateral sclerosis: a meta-analysis study |
title_full | Increased peripheral blood inflammatory cytokine levels in amyotrophic lateral sclerosis: a meta-analysis study |
title_fullStr | Increased peripheral blood inflammatory cytokine levels in amyotrophic lateral sclerosis: a meta-analysis study |
title_full_unstemmed | Increased peripheral blood inflammatory cytokine levels in amyotrophic lateral sclerosis: a meta-analysis study |
title_short | Increased peripheral blood inflammatory cytokine levels in amyotrophic lateral sclerosis: a meta-analysis study |
title_sort | increased peripheral blood inflammatory cytokine levels in amyotrophic lateral sclerosis: a meta-analysis study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567306/ https://www.ncbi.nlm.nih.gov/pubmed/28831083 http://dx.doi.org/10.1038/s41598-017-09097-1 |
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