Anti-GQ1b Antibody Syndrome with Visual Impairment: A Retrospective Case Series

Background: Anti-GQ1b antibody syndrome referred to a clinical spectrum characterized by acute onset of ataxia, ophthalmoplegia and areflexia, while visual deterioration was rarely reported in terms of ocular disorders. This study aimed to describe the clinical characteristics of anti-GQ1b antibody...

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Main Authors: Qing Zeng, Juan Li, Shu-Xing Feng, Pei-Yao Xiao, Yi-Fan Zheng, Cheng Zhang, Song-Jie Liao
Format: Article
Language:English
Published: IMR Press 2022-04-01
Series:Journal of Integrative Neuroscience
Subjects:
Online Access:https://www.imrpress.com/journal/JIN/21/3/10.31083/j.jin2103081
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author Qing Zeng
Juan Li
Shu-Xing Feng
Pei-Yao Xiao
Yi-Fan Zheng
Cheng Zhang
Song-Jie Liao
author_facet Qing Zeng
Juan Li
Shu-Xing Feng
Pei-Yao Xiao
Yi-Fan Zheng
Cheng Zhang
Song-Jie Liao
author_sort Qing Zeng
collection DOAJ
description Background: Anti-GQ1b antibody syndrome referred to a clinical spectrum characterized by acute onset of ataxia, ophthalmoplegia and areflexia, while visual deterioration was rarely reported in terms of ocular disorders. This study aimed to describe the clinical characteristics of anti-GQ1b antibody syndrome with visual impairment. Methods: The database at the First Affiliated Hospital of Sun Yat-sen University was searched from 2014 to 2020. Patients with anti-GQ1b IgG were identified and divided into two groups according to the existence of optic neuropathy. Clinical and laboratory data of these subjects between the two groups were collected and analyzed. All patients were followed up by telephone to assess the outcome. Results: A total of 12 patients with seropositive anti-GQ1b antibody were included, 75% of which got antecedent infection. Of these cases, 3 showed visual deterioration accompanied by abnormal orbital magnetic resonance imaging or visual evoked potentials, and the other 9 didn’t show any evidence of vision impairment. Patients in the optic neuropathy group presented prominent visual impairments as initial symptoms and were more likely to suffer from facial weakness. There were 4 patients in normal visual acuity group complaining of blurred vision due to intraocular muscle paralysis, which was distinguished by subsequent examination. The combination of glucocorticoids and intravenous immunoglobulin was applied to treat patients with optic neuropathy. Conclusions: This study provides strong evidence that anti-GQ1b antibody syndrome can exhibit visual impairment, which helps further expand the clinical spectrum of anti-GQ1b antibody syndrome. More attention should be paid to the physical and supplementary ophthalmological examination to explore the pathogenesis and treatment of anti-GQ1b antibody syndrome.
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spelling doaj.art-e8ac197b823a48588a1094de8e3b02ba2022-12-22T02:27:59ZengIMR PressJournal of Integrative Neuroscience0219-63522022-04-012138110.31083/j.jin2103081S0219-6352(22)00341-2Anti-GQ1b Antibody Syndrome with Visual Impairment: A Retrospective Case SeriesQing Zeng0Juan Li1Shu-Xing Feng2Pei-Yao Xiao3Yi-Fan Zheng4Cheng Zhang5Song-Jie Liao6Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University; Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases, National Key Clinical Department and Key Discipline of Neurology, 510080 Guangzhou, Guangdong, ChinaDepartment of Neurology, Xi'an People's Hospital (Xi'an Fourth Hospital), Affiliated Guangren Hospital, School of Medicine, Xi'an Jiao tong University, 710004 Xi'an, Shaanxi, ChinaDepartment of Function Examination, Zhongshan Hospital of Traditional Chinese Medicine, 528400 Zhongshan, Guangdong, ChinaDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University; Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases, National Key Clinical Department and Key Discipline of Neurology, 510080 Guangzhou, Guangdong, ChinaDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University; Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases, National Key Clinical Department and Key Discipline of Neurology, 510080 Guangzhou, Guangdong, ChinaDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University; Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases, National Key Clinical Department and Key Discipline of Neurology, 510080 Guangzhou, Guangdong, ChinaDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University; Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases, National Key Clinical Department and Key Discipline of Neurology, 510080 Guangzhou, Guangdong, ChinaBackground: Anti-GQ1b antibody syndrome referred to a clinical spectrum characterized by acute onset of ataxia, ophthalmoplegia and areflexia, while visual deterioration was rarely reported in terms of ocular disorders. This study aimed to describe the clinical characteristics of anti-GQ1b antibody syndrome with visual impairment. Methods: The database at the First Affiliated Hospital of Sun Yat-sen University was searched from 2014 to 2020. Patients with anti-GQ1b IgG were identified and divided into two groups according to the existence of optic neuropathy. Clinical and laboratory data of these subjects between the two groups were collected and analyzed. All patients were followed up by telephone to assess the outcome. Results: A total of 12 patients with seropositive anti-GQ1b antibody were included, 75% of which got antecedent infection. Of these cases, 3 showed visual deterioration accompanied by abnormal orbital magnetic resonance imaging or visual evoked potentials, and the other 9 didn’t show any evidence of vision impairment. Patients in the optic neuropathy group presented prominent visual impairments as initial symptoms and were more likely to suffer from facial weakness. There were 4 patients in normal visual acuity group complaining of blurred vision due to intraocular muscle paralysis, which was distinguished by subsequent examination. The combination of glucocorticoids and intravenous immunoglobulin was applied to treat patients with optic neuropathy. Conclusions: This study provides strong evidence that anti-GQ1b antibody syndrome can exhibit visual impairment, which helps further expand the clinical spectrum of anti-GQ1b antibody syndrome. More attention should be paid to the physical and supplementary ophthalmological examination to explore the pathogenesis and treatment of anti-GQ1b antibody syndrome.https://www.imrpress.com/journal/JIN/21/3/10.31083/j.jin2103081gq1b gangliosidemiller fisher syndromeguillain-barré syndromevision disordersoptic neuritis
spellingShingle Qing Zeng
Juan Li
Shu-Xing Feng
Pei-Yao Xiao
Yi-Fan Zheng
Cheng Zhang
Song-Jie Liao
Anti-GQ1b Antibody Syndrome with Visual Impairment: A Retrospective Case Series
Journal of Integrative Neuroscience
gq1b ganglioside
miller fisher syndrome
guillain-barré syndrome
vision disorders
optic neuritis
title Anti-GQ1b Antibody Syndrome with Visual Impairment: A Retrospective Case Series
title_full Anti-GQ1b Antibody Syndrome with Visual Impairment: A Retrospective Case Series
title_fullStr Anti-GQ1b Antibody Syndrome with Visual Impairment: A Retrospective Case Series
title_full_unstemmed Anti-GQ1b Antibody Syndrome with Visual Impairment: A Retrospective Case Series
title_short Anti-GQ1b Antibody Syndrome with Visual Impairment: A Retrospective Case Series
title_sort anti gq1b antibody syndrome with visual impairment a retrospective case series
topic gq1b ganglioside
miller fisher syndrome
guillain-barré syndrome
vision disorders
optic neuritis
url https://www.imrpress.com/journal/JIN/21/3/10.31083/j.jin2103081
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AT peiyaoxiao antigq1bantibodysyndromewithvisualimpairmentaretrospectivecaseseries
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