Clinical characteristics of patients with myasthenia gravis associated with other autoimmune diseases

<p><strong>Objective</strong> To analyze the clinical characteristics, drug efficacy and prognosis of patients with myasthenia gravis (MG) associated with other autoimmune diseases. <strong>Methods</strong> Eighty-three MG patients were divided into 2 groups. One gro...

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Main Authors: Li-li WANG, Yun ZHANG, Mao-lin HE, Xian-hao XU
Format: Article
Language:English
Published: Tianjin Huanhu Hospital 2014-10-01
Series:Chinese Journal of Contemporary Neurology and Neurosurgery
Subjects:
Online Access:http://www.cjcnn.org/index.php/cjcnn/article/view/1057
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spelling doaj-dc4e2fe43635433785f629d31753c73c2020-11-24T21:45:41ZengTianjin Huanhu HospitalChinese Journal of Contemporary Neurology and Neurosurgery1672-67312014-10-0114108738771053Clinical characteristics of patients with myasthenia gravis associated with other autoimmune diseasesLi-li WANG0Yun ZHANG1Mao-lin HE2Xian-hao XU3Department of Neurology and Psychiatry, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, ChinaDepartment of Neurology and Psychiatry, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, ChinaDepartment of Neurology and Psychiatry, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, ChinaDepartment of Neurology, Beijing Hospital, Beijing 100730, China<p><strong>Objective</strong> To analyze the clinical characteristics, drug efficacy and prognosis of patients with myasthenia gravis (MG) associated with other autoimmune diseases. <strong>Methods</strong> Eighty-three MG patients were divided into 2 groups. One group included MG patients with autoimmune diseases (AIDMG, N = 24), and the other included MG patients without autoimmune diseases (NAIDMG, N = 59). Firstly, clinical features such as sex, age of onset, initial symptoms and thymus abnormalities were compared between patients with AIDMG and NAIDMG. Secondly, effect of different therapies, including pyridostigmine, corticosteroids, immunoglobulin, immunosuppressants and thymectomy was compared between 2 groups. Finally, prognosis including relapse rate and recurrence time during the first 2 years after MG onset was compared. Whether and when ocular myasthenia gravis (OMG) progressing to general myasthenia gravis (GMG) and the first onset of GMG symptoms during the first 2 years were also compared between 2 groups.  <strong>Results</strong> The difference of gender predominance (<em>χ<sup>2</sup></em> = 8.467, <em>P</em> = 0.004), ptosis affecting left or right or both sides (<em>χ<sup>2</sup></em> = 9.830, <em>P</em> = 0.007) and disease course within 2 years after onset (<em>χ<sup>2</sup></em> = 15.255, <em>P</em> = 0.001) between AIDMG group and NAIDMG group were statistically significant. Other clinical features such as age of onset (<em>χ<sup>2</sup></em> = 1.728, <em>P</em> = 0.228), initial symptoms (<em>χ<sup>2</sup></em> = 0.252, <em>P</em> = 0.791), thymus abnormalities (<em>χ<sup>2</sup></em> = 3.200, <em>P</em> = 0.202) were not significantly different between 2 groups. Differences of therapeutical effect such as pyridostigmine (<em>χ<sup>2</sup></em> = 0.411, <em>P</em> = 0.395), corticosteroids (<em>χ<sup>2</sup></em> = 0.156, <em>P</em> = 0.513), immunoglobulin (<em>χ<sup>2</sup></em> = 0.359, <em>P</em> = 0.462), immunosuppressants (<em>χ<sup>2</sup></em> = 0.081, <em>P</em> = 0.526) and thymectomy (<em>χ<sup>2</sup></em> = 0.337, <em>P</em> = 0.391) between 2 groups were not statistically significant. The ratio of OMG progressing to GMG (<em>χ<sup>2</sup></em> = 1.826, <em>P</em> = 0.148), time of progressing (Fisher's exact test: <em>P</em> = 0.639), first onset symptom (Fisher's exact test: <em>P</em> = 0.196) and recurrence time (Fisher's exact test: <em>P</em> = 1.000) were not significantly different between 2 groups. <strong>Conclusions</strong> AIDMG was more common in female patients. Bilateral ptosis involvement at the same time was more common in AIDMG. Relapse rate during the first 2 years after MG onset was higher in AIDMG than that in NAIDMG.</p><p> </p><p><strong>doi: </strong>10.3969/j.issn.1672-6731.2014.10.009</p>http://www.cjcnn.org/index.php/cjcnn/article/view/1057Myasthenia gravisAutoimmune diseases
collection DOAJ
language English
format Article
sources DOAJ
author Li-li WANG
Yun ZHANG
Mao-lin HE
Xian-hao XU
spellingShingle Li-li WANG
Yun ZHANG
Mao-lin HE
Xian-hao XU
Clinical characteristics of patients with myasthenia gravis associated with other autoimmune diseases
Chinese Journal of Contemporary Neurology and Neurosurgery
Myasthenia gravis
Autoimmune diseases
author_facet Li-li WANG
Yun ZHANG
Mao-lin HE
Xian-hao XU
author_sort Li-li WANG
title Clinical characteristics of patients with myasthenia gravis associated with other autoimmune diseases
title_short Clinical characteristics of patients with myasthenia gravis associated with other autoimmune diseases
title_full Clinical characteristics of patients with myasthenia gravis associated with other autoimmune diseases
title_fullStr Clinical characteristics of patients with myasthenia gravis associated with other autoimmune diseases
title_full_unstemmed Clinical characteristics of patients with myasthenia gravis associated with other autoimmune diseases
title_sort clinical characteristics of patients with myasthenia gravis associated with other autoimmune diseases
publisher Tianjin Huanhu Hospital
series Chinese Journal of Contemporary Neurology and Neurosurgery
issn 1672-6731
publishDate 2014-10-01
description <p><strong>Objective</strong> To analyze the clinical characteristics, drug efficacy and prognosis of patients with myasthenia gravis (MG) associated with other autoimmune diseases. <strong>Methods</strong> Eighty-three MG patients were divided into 2 groups. One group included MG patients with autoimmune diseases (AIDMG, N = 24), and the other included MG patients without autoimmune diseases (NAIDMG, N = 59). Firstly, clinical features such as sex, age of onset, initial symptoms and thymus abnormalities were compared between patients with AIDMG and NAIDMG. Secondly, effect of different therapies, including pyridostigmine, corticosteroids, immunoglobulin, immunosuppressants and thymectomy was compared between 2 groups. Finally, prognosis including relapse rate and recurrence time during the first 2 years after MG onset was compared. Whether and when ocular myasthenia gravis (OMG) progressing to general myasthenia gravis (GMG) and the first onset of GMG symptoms during the first 2 years were also compared between 2 groups.  <strong>Results</strong> The difference of gender predominance (<em>χ<sup>2</sup></em> = 8.467, <em>P</em> = 0.004), ptosis affecting left or right or both sides (<em>χ<sup>2</sup></em> = 9.830, <em>P</em> = 0.007) and disease course within 2 years after onset (<em>χ<sup>2</sup></em> = 15.255, <em>P</em> = 0.001) between AIDMG group and NAIDMG group were statistically significant. Other clinical features such as age of onset (<em>χ<sup>2</sup></em> = 1.728, <em>P</em> = 0.228), initial symptoms (<em>χ<sup>2</sup></em> = 0.252, <em>P</em> = 0.791), thymus abnormalities (<em>χ<sup>2</sup></em> = 3.200, <em>P</em> = 0.202) were not significantly different between 2 groups. Differences of therapeutical effect such as pyridostigmine (<em>χ<sup>2</sup></em> = 0.411, <em>P</em> = 0.395), corticosteroids (<em>χ<sup>2</sup></em> = 0.156, <em>P</em> = 0.513), immunoglobulin (<em>χ<sup>2</sup></em> = 0.359, <em>P</em> = 0.462), immunosuppressants (<em>χ<sup>2</sup></em> = 0.081, <em>P</em> = 0.526) and thymectomy (<em>χ<sup>2</sup></em> = 0.337, <em>P</em> = 0.391) between 2 groups were not statistically significant. The ratio of OMG progressing to GMG (<em>χ<sup>2</sup></em> = 1.826, <em>P</em> = 0.148), time of progressing (Fisher's exact test: <em>P</em> = 0.639), first onset symptom (Fisher's exact test: <em>P</em> = 0.196) and recurrence time (Fisher's exact test: <em>P</em> = 1.000) were not significantly different between 2 groups. <strong>Conclusions</strong> AIDMG was more common in female patients. Bilateral ptosis involvement at the same time was more common in AIDMG. Relapse rate during the first 2 years after MG onset was higher in AIDMG than that in NAIDMG.</p><p> </p><p><strong>doi: </strong>10.3969/j.issn.1672-6731.2014.10.009</p>
topic Myasthenia gravis
Autoimmune diseases
url http://www.cjcnn.org/index.php/cjcnn/article/view/1057
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