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Antecedent infections in Guillain‐Barré syndrome: a single‐center, prospective study
OBJECTIVE: To investigate the spectrum of antecedent infections in Chinese patients with Guillain‐Barré syndrome (GBS) and analyze the infections‐related clinical phenotypes locally. METHODS: A prospective case‐control study of 150 patients diagnosed with GBS and age‐ and sex‐matched neurological an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917331/ https://www.ncbi.nlm.nih.gov/pubmed/31714025 http://dx.doi.org/10.1002/acn3.50946 |
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author | Hao, Yanlei Wang, Weifang Jacobs, Bart C. Qiao, Baojun Chen, Mengshi Liu, Daiqiang Feng, Xungang Wang, Yuzhong |
author_facet | Hao, Yanlei Wang, Weifang Jacobs, Bart C. Qiao, Baojun Chen, Mengshi Liu, Daiqiang Feng, Xungang Wang, Yuzhong |
author_sort | Hao, Yanlei |
collection | PubMed |
description | OBJECTIVE: To investigate the spectrum of antecedent infections in Chinese patients with Guillain‐Barré syndrome (GBS) and analyze the infections‐related clinical phenotypes locally. METHODS: A prospective case‐control study of 150 patients diagnosed with GBS and age‐ and sex‐matched neurological and healthy controls was performed to investigate recent infections of 14 pathogens serologically and collect the clinical data during a follow‐up of 12 months. RESULTS: In total, 53% of patients with GBS had a positive serology for recent infection, including Campylobacter jejuni (27%), influenza A (17%) and B (16%), hepatitis A virus (5%), dengue virus (3%), cytomegalovirus (3%), Epstein–Barr virus (3%), Mycoplasma pneumoniae (2%), herpes simplex virus (2%), varicella‐zoster virus (1%), and rubella virus (1%). Serology for infections of hepatitis E virus, Haemophilus influenzae, and Zika virus was negative. There was a higher frequency of C. jejuni, influenza A, influenza B, and hepatitis A virus infections in GBS patients than both the neurological and healthy controls. C. jejuni infection was more frequent in younger GBS patients and was associated with antibodies against GM1, GalNAc‐GD1a, and GM1:galactocerebroside complex. Influenza B infection was associated with a pure motor form of GBS. INTERPRETATION: C. jejuni, influenza A, influenza B, and hepatitis A virus serve as the most common cause of antecedent infections in GBS locally. Influenza B‐related GBS may represent a pure motor phenotype. Differences in the infectious spectrum worldwide may contribute to the geographical clinical heterogeneity of GBS. |
format | Online Article Text |
id | pubmed-6917331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69173312019-12-23 Antecedent infections in Guillain‐Barré syndrome: a single‐center, prospective study Hao, Yanlei Wang, Weifang Jacobs, Bart C. Qiao, Baojun Chen, Mengshi Liu, Daiqiang Feng, Xungang Wang, Yuzhong Ann Clin Transl Neurol Research Articles OBJECTIVE: To investigate the spectrum of antecedent infections in Chinese patients with Guillain‐Barré syndrome (GBS) and analyze the infections‐related clinical phenotypes locally. METHODS: A prospective case‐control study of 150 patients diagnosed with GBS and age‐ and sex‐matched neurological and healthy controls was performed to investigate recent infections of 14 pathogens serologically and collect the clinical data during a follow‐up of 12 months. RESULTS: In total, 53% of patients with GBS had a positive serology for recent infection, including Campylobacter jejuni (27%), influenza A (17%) and B (16%), hepatitis A virus (5%), dengue virus (3%), cytomegalovirus (3%), Epstein–Barr virus (3%), Mycoplasma pneumoniae (2%), herpes simplex virus (2%), varicella‐zoster virus (1%), and rubella virus (1%). Serology for infections of hepatitis E virus, Haemophilus influenzae, and Zika virus was negative. There was a higher frequency of C. jejuni, influenza A, influenza B, and hepatitis A virus infections in GBS patients than both the neurological and healthy controls. C. jejuni infection was more frequent in younger GBS patients and was associated with antibodies against GM1, GalNAc‐GD1a, and GM1:galactocerebroside complex. Influenza B infection was associated with a pure motor form of GBS. INTERPRETATION: C. jejuni, influenza A, influenza B, and hepatitis A virus serve as the most common cause of antecedent infections in GBS locally. Influenza B‐related GBS may represent a pure motor phenotype. Differences in the infectious spectrum worldwide may contribute to the geographical clinical heterogeneity of GBS. John Wiley and Sons Inc. 2019-11-12 /pmc/articles/PMC6917331/ /pubmed/31714025 http://dx.doi.org/10.1002/acn3.50946 Text en © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. 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 | Research Articles Hao, Yanlei Wang, Weifang Jacobs, Bart C. Qiao, Baojun Chen, Mengshi Liu, Daiqiang Feng, Xungang Wang, Yuzhong Antecedent infections in Guillain‐Barré syndrome: a single‐center, prospective study |
title | Antecedent infections in Guillain‐Barré syndrome: a single‐center, prospective study |
title_full | Antecedent infections in Guillain‐Barré syndrome: a single‐center, prospective study |
title_fullStr | Antecedent infections in Guillain‐Barré syndrome: a single‐center, prospective study |
title_full_unstemmed | Antecedent infections in Guillain‐Barré syndrome: a single‐center, prospective study |
title_short | Antecedent infections in Guillain‐Barré syndrome: a single‐center, prospective study |
title_sort | antecedent infections in guillain‐barré syndrome: a single‐center, prospective study |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917331/ https://www.ncbi.nlm.nih.gov/pubmed/31714025 http://dx.doi.org/10.1002/acn3.50946 |
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