Clinical analysis of ocular myasthenia gravis

Objective To study clinical characteristics of ocular myasthenia gravis (OMG) to provide evidence for diagnosis and treatment of this disease. Methods Clinical data of 113 OMG patients were retrospectively analysed. Immunofluoresence cell staining was applied to detect the acetylcholine receptor (AC...

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Main Authors: Xiaowei MA, Li YANG, Chunsheng YANG, Daqi ZHANG, Hui ZHAI, Yan CHENG
Format: Article
Language:English
Published: Tianjin Huanhu Hospital 2011-02-01
Series:Chinese Journal of Contemporary Neurology and Neurosurgery
Subjects:
Online Access:http://www.cjcnn.org/index.php/cjcnn/article/view/320
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spelling doaj-91097a6216374ddc97b3bf70e67becb12020-11-25T00:16:17ZengTianjin Huanhu HospitalChinese Journal of Contemporary Neurology and Neurosurgery1672-67312011-02-011118892319Clinical analysis of ocular myasthenia gravisXiaowei MALi YANGChunsheng YANGDaqi ZHANGHui ZHAIYan CHENGObjective To study clinical characteristics of ocular myasthenia gravis (OMG) to provide evidence for diagnosis and treatment of this disease. Methods Clinical data of 113 OMG patients were retrospectively analysed. Immunofluoresence cell staining was applied to detect the acetylcholine receptor (AChR) antibody and muscle ⁃ specific receptor tyrosine kinase (MuSK) antibody, and their predictive value for developing to generalized myasthenia gravis (MG) was assessed. Results Adult⁃onset of OMG was often happened in males over age 40. The most common initial presentation was ptosis (n = 95, 84.07% ), and a few started with diplopia (n = 18, 15.93% ). The positive ratio of fatigue test and neostigmine test was 79.44% (85/107) and 84.85% (84/99) respectively, abnormal rate of repetitive nerve stimulation (RNS) and serum thyroid antibodies was 44.32% (39/88) and 28% (14/50) respectively. The incidence of thymic hyperplasia and thymoma was 16.67% (17/102) and 11.76% (12/102), respectively. The positive rate of serum AChR antibody was 62.83% (71/113), but the serum MuSK antibody was negative in all patients. There were 12.39% (14/113) OMG patients progressed to generalized MG. Patients with higher AChR antibody expression were with more risk to progress to generalized MG (χ2 = 4.587, P = 0.032). Conclusion Adult ⁃ onset OMG often begins in middle ⁃ aged males. The main manifestation of OMG are ptosis and diplopia. Most patients are associated with abnormality of thymus and thyroid. Patients with higher AChR antibody expression are more at risk for progressing to generalized MG. MuSK antibody is uncommon in OMG. DOI:10.3969/j.issn.1672-6731.2011.01.018http://www.cjcnn.org/index.php/cjcnn/article/view/320Myasthenia gravisOphthalmoplegiaReceptors, cholinergicElectric stimulationFluorescent antibody technique
collection DOAJ
language English
format Article
sources DOAJ
author Xiaowei MA
Li YANG
Chunsheng YANG
Daqi ZHANG
Hui ZHAI
Yan CHENG
spellingShingle Xiaowei MA
Li YANG
Chunsheng YANG
Daqi ZHANG
Hui ZHAI
Yan CHENG
Clinical analysis of ocular myasthenia gravis
Chinese Journal of Contemporary Neurology and Neurosurgery
Myasthenia gravis
Ophthalmoplegia
Receptors, cholinergic
Electric stimulation
Fluorescent antibody technique
author_facet Xiaowei MA
Li YANG
Chunsheng YANG
Daqi ZHANG
Hui ZHAI
Yan CHENG
author_sort Xiaowei MA
title Clinical analysis of ocular myasthenia gravis
title_short Clinical analysis of ocular myasthenia gravis
title_full Clinical analysis of ocular myasthenia gravis
title_fullStr Clinical analysis of ocular myasthenia gravis
title_full_unstemmed Clinical analysis of ocular myasthenia gravis
title_sort clinical analysis of ocular myasthenia gravis
publisher Tianjin Huanhu Hospital
series Chinese Journal of Contemporary Neurology and Neurosurgery
issn 1672-6731
publishDate 2011-02-01
description Objective To study clinical characteristics of ocular myasthenia gravis (OMG) to provide evidence for diagnosis and treatment of this disease. Methods Clinical data of 113 OMG patients were retrospectively analysed. Immunofluoresence cell staining was applied to detect the acetylcholine receptor (AChR) antibody and muscle ⁃ specific receptor tyrosine kinase (MuSK) antibody, and their predictive value for developing to generalized myasthenia gravis (MG) was assessed. Results Adult⁃onset of OMG was often happened in males over age 40. The most common initial presentation was ptosis (n = 95, 84.07% ), and a few started with diplopia (n = 18, 15.93% ). The positive ratio of fatigue test and neostigmine test was 79.44% (85/107) and 84.85% (84/99) respectively, abnormal rate of repetitive nerve stimulation (RNS) and serum thyroid antibodies was 44.32% (39/88) and 28% (14/50) respectively. The incidence of thymic hyperplasia and thymoma was 16.67% (17/102) and 11.76% (12/102), respectively. The positive rate of serum AChR antibody was 62.83% (71/113), but the serum MuSK antibody was negative in all patients. There were 12.39% (14/113) OMG patients progressed to generalized MG. Patients with higher AChR antibody expression were with more risk to progress to generalized MG (χ2 = 4.587, P = 0.032). Conclusion Adult ⁃ onset OMG often begins in middle ⁃ aged males. The main manifestation of OMG are ptosis and diplopia. Most patients are associated with abnormality of thymus and thyroid. Patients with higher AChR antibody expression are more at risk for progressing to generalized MG. MuSK antibody is uncommon in OMG. DOI:10.3969/j.issn.1672-6731.2011.01.018
topic Myasthenia gravis
Ophthalmoplegia
Receptors, cholinergic
Electric stimulation
Fluorescent antibody technique
url http://www.cjcnn.org/index.php/cjcnn/article/view/320
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