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Association of neurofascin IgG4 and atypical chronic inflammatory demyelinating polyneuropathy: A systematic review and meta‐analysis

BACKGROUND: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is the most commonly observed phenotype among chronic acquired demyelinating polyneuropathies and is clinically variable. The aim of this meta‐analysis was to evaluate the diagnostic value and characteristics of CIDP target...

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Autores principales: Hu, Wenyu, Xin, Yanguo, He, Zhiyi, Zhao, Yinan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192399/
https://www.ncbi.nlm.nih.gov/pubmed/30240176
http://dx.doi.org/10.1002/brb3.1115
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author Hu, Wenyu
Xin, Yanguo
He, Zhiyi
Zhao, Yinan
author_facet Hu, Wenyu
Xin, Yanguo
He, Zhiyi
Zhao, Yinan
author_sort Hu, Wenyu
collection PubMed
description BACKGROUND: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is the most commonly observed phenotype among chronic acquired demyelinating polyneuropathies and is clinically variable. The aim of this meta‐analysis was to evaluate the diagnostic value and characteristics of CIDP targeting neurofascin 155 (NF155). METHODS: A systematic literature search was performed on March 2018, and two reviewers independently extracted data and assessed the risk of bias on MEDLINE, EMBASE, the Web of Science, and the Cochrane Library to identify relevant articles. RESULTS: Ten articles for the NF155 protein test with 1,161 patients and 1,636 controls were identified. The results showed that the pooled sensitivity was 0.09 (95% CI: 0.06–015), and specificity was 1.00 (95% CI: 0.98–1.00) of the NF155 for CIDP. The meta‐analysis revealed that the sensory ataxic occurrence rate (OR: 10.79, 95% CI: 5.24–22.22) and tremor occurrence rate (OR: 6.71, 95% CI: 3.37–13.39) were higher among patients positive for NF155 compared with NF155‐negative CIDP patients. However, the rate of good treatment response to intravenous immunoglobulin (IVIg) (OR: 0.09, 95% CI: 0.02–0.42) was lower in NF155‐positive CIDP patients. CONCLUSIONS: NF155 is a specific protein marker for CIDP, but its diagnostic value has been questioned due to low sensitivity. However, as an antibody against paranodal antigens, NF155 seems more valuable in defining clinical subsets of CIDP.
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spelling pubmed-61923992018-10-22 Association of neurofascin IgG4 and atypical chronic inflammatory demyelinating polyneuropathy: A systematic review and meta‐analysis Hu, Wenyu Xin, Yanguo He, Zhiyi Zhao, Yinan Brain Behav Original Research BACKGROUND: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is the most commonly observed phenotype among chronic acquired demyelinating polyneuropathies and is clinically variable. The aim of this meta‐analysis was to evaluate the diagnostic value and characteristics of CIDP targeting neurofascin 155 (NF155). METHODS: A systematic literature search was performed on March 2018, and two reviewers independently extracted data and assessed the risk of bias on MEDLINE, EMBASE, the Web of Science, and the Cochrane Library to identify relevant articles. RESULTS: Ten articles for the NF155 protein test with 1,161 patients and 1,636 controls were identified. The results showed that the pooled sensitivity was 0.09 (95% CI: 0.06–015), and specificity was 1.00 (95% CI: 0.98–1.00) of the NF155 for CIDP. The meta‐analysis revealed that the sensory ataxic occurrence rate (OR: 10.79, 95% CI: 5.24–22.22) and tremor occurrence rate (OR: 6.71, 95% CI: 3.37–13.39) were higher among patients positive for NF155 compared with NF155‐negative CIDP patients. However, the rate of good treatment response to intravenous immunoglobulin (IVIg) (OR: 0.09, 95% CI: 0.02–0.42) was lower in NF155‐positive CIDP patients. CONCLUSIONS: NF155 is a specific protein marker for CIDP, but its diagnostic value has been questioned due to low sensitivity. However, as an antibody against paranodal antigens, NF155 seems more valuable in defining clinical subsets of CIDP. John Wiley and Sons Inc. 2018-09-21 /pmc/articles/PMC6192399/ /pubmed/30240176 http://dx.doi.org/10.1002/brb3.1115 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Hu, Wenyu
Xin, Yanguo
He, Zhiyi
Zhao, Yinan
Association of neurofascin IgG4 and atypical chronic inflammatory demyelinating polyneuropathy: A systematic review and meta‐analysis
title Association of neurofascin IgG4 and atypical chronic inflammatory demyelinating polyneuropathy: A systematic review and meta‐analysis
title_full Association of neurofascin IgG4 and atypical chronic inflammatory demyelinating polyneuropathy: A systematic review and meta‐analysis
title_fullStr Association of neurofascin IgG4 and atypical chronic inflammatory demyelinating polyneuropathy: A systematic review and meta‐analysis
title_full_unstemmed Association of neurofascin IgG4 and atypical chronic inflammatory demyelinating polyneuropathy: A systematic review and meta‐analysis
title_short Association of neurofascin IgG4 and atypical chronic inflammatory demyelinating polyneuropathy: A systematic review and meta‐analysis
title_sort association of neurofascin igg4 and atypical chronic inflammatory demyelinating polyneuropathy: a systematic review and meta‐analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192399/
https://www.ncbi.nlm.nih.gov/pubmed/30240176
http://dx.doi.org/10.1002/brb3.1115
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