Literature DB >> 23252901

Management challenges in muscle-specific tyrosine kinase myasthenia gravis.

Amelia Evoli1, Paolo E Alboini, Ana Bisonni, Alessia Mastrorosa, Emanuela Bartoccioni, Emanuela Bartocccioni.   

Abstract

Myasthenia gravis with antibodies to muscle-specific tyrosine kinase (MuSK-MG) is generally considered a severe disease because of the associated weakness distribution with prevalent involvement of bulbar muscles and a rapidly progressive course and early respiratory crises. Its treatment can be unrewarding, owing to poor response to acetylcholinesterase inhibitors in most patients, disease relapses in spite of high-dose immunosuppression, and development of permanent bulbar weakness. High-dose prednisone plus plasma exchange is the recommended approach for treating rapidly progressive bulbar weakness. In the disease management, oral steroids proved effective, plasma exchange produced marked, albeit short-term, improvement, while conventional immunosuppressants were comparatively less effective. Rituximab is a promising treatment for refractory MuSK-MG; in uncontrolled studies, nearly all treated patients achieved significant improvement with substantial decrease of medication. It is yet to be clarified whether the early use of rituximab could prevent the permanent bulbar weakness, which constitutes a relevant disability in these patients.
© 2012 New York Academy of Sciences.

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Year:  2012        PMID: 23252901     DOI: 10.1111/j.1749-6632.2012.06781.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  8 in total

1.  Marked phenotypic variability in two siblings with congenital myasthenic syndrome due to mutations in MUSK.

Authors:  Lorenzo Maggi; R Brugnoni; V Scaioli; T L Winden; L Morandi; A G Engel; R Mantegazza; P Bernasconi
Journal:  J Neurol       Date:  2013-10-12       Impact factor: 4.849

2.  Autoantibody-producing plasmablasts after B cell depletion identified in muscle-specific kinase myasthenia gravis.

Authors:  Panos Stathopoulos; Aditya Kumar; Richard J Nowak; Kevin C O'Connor
Journal:  JCI Insight       Date:  2017-09-07

3.  Treatment of MuSK-Associated Myasthenia Gravis.

Authors:  Khalid El-Salem; Ahmed Yassin; Kefah Al-Hayk; Salma Yahya; Duha Al-Shorafat; Said S Dahbour
Journal:  Curr Treat Options Neurol       Date:  2014-04       Impact factor: 3.972

Review 4.  Myasthenia Gravis: Pathogenic Effects of Autoantibodies on Neuromuscular Architecture.

Authors:  Inga Koneczny; Ruth Herbst
Journal:  Cells       Date:  2019-07-02       Impact factor: 6.600

5.  Long-Lasting Rituximab-Induced Reduction of Specific-But Not Total-IgG4 in MuSK-Positive Myasthenia Gravis.

Authors:  Mariapaola Marino; Umberto Basile; Gregorio Spagni; Cecilia Napodano; Raffaele Iorio; Francesca Gulli; Laura Todi; Carlo Provenzano; Emanuela Bartoccioni; Amelia Evoli
Journal:  Front Immunol       Date:  2020-05-05       Impact factor: 7.561

6.  Factors affecting minimal manifestation status induction in myasthenia gravis.

Authors:  Yi Li; Shumei Yang; Xiaohua Dong; Zhibin Li; Yuyao Peng; Wanlin Jin; Di Chen; Ran Zhou; Fei Jiang; Chengkai Yan; Huan Yang
Journal:  Ther Adv Neurol Disord       Date:  2022-03-29       Impact factor: 6.570

7.  Clinical Features of Myasthenia Gravis With Antibodies to MuSK Based on Age at Onset: A Multicenter Retrospective Study in China.

Authors:  Yufan Zhou; Jialin Chen; Zunbo Li; Song Tan; Chong Yan; Sushan Luo; Lei Zhou; Jie Song; Xiao Huan; Ying Wang; Chongbo Zhao; Wenshuang Zeng; Jianying Xi
Journal:  Front Neurol       Date:  2022-04-08       Impact factor: 4.003

8.  Long-Term Efficacy of Non-steroid Immunosuppressive Agents in Anti-Muscle-Specific Kinase Positive Myasthenia Gravis Patients: A Prospective Study.

Authors:  Ying Tan; Jiayu Shi; Yangyu Huang; Ke Li; Jingwen Yan; Li Zhu; Yuzhou Guan; Liying Cui
Journal:  Front Neurol       Date:  2022-06-13       Impact factor: 4.086

  8 in total

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