Myasthenia Gravis-An Analysis of Multimodal Evoked Potentials

被引:3
作者
Dziadkowiak, Edyta [1 ]
Waliszewska-Prosol, Marta [1 ]
Wieczorek, Malgorzata [2 ]
Bladowska, Joanna [3 ]
Budrewicz, Slawomir [1 ]
Ejma, Maria [1 ]
机构
[1] Wroclaw Med Univ, Dept Neurol, PL-50556 Wroclaw, Poland
[2] Univ Wroclaw, Fac Earth Sci & Environm Management, PL-50137 Wroclaw, Poland
[3] Wroclaw Med Univ, Dept Gen Radiol Intervent Radiol & Neuroradiol, PL-50556 Wroclaw, Poland
关键词
myasthenia gravis; visual evoked potentials; brainstem auditory evoked potentials; somatosensory evoked potentials; INFLAMMATORY DEMYELINATING POLYNEUROPATHY; AUTOANTIBODIES; STIMULATION;
D O I
10.3390/brainsci11081057
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Introduction: The aim of this study is a comprehensive analysis of the parameters of exogenous evoked potentials (visual, brainstem auditory, and somatosensory) in patients with myasthenia gravis (MG), a prototype of both neuromuscular junction disease and autoimmune disease. The study also seeks to isolate electrophysiological changes that may indicate disorders within the central and/or peripheral nervous system. Methods: A total of forty-two consecutive patients with myasthenia gravis (24 women, 18 men) were included in the study. All of the patients underwent EP examination. MR images were also analyzed. Results: In the group of MG patients, the latency of P100 (113.9 +/- 13.9; p < 0.0001) VEP, wave III (3.92 +/- 0.29; p = 0.015), wave V (5.93 +/- 0.32; <0.0001), interlatency III-V (2.00 +/- 0.12; p < 0.0001), interlatency I-V (4.20 +/- 0.28; p < 0.001) BAEP, and all components of SEP (N9, P10, N13, P16, N20, P22) were significantly longer. Mean wave I and V amplitude BAEP were relatively lower. Conclusions: The results of the study suggest the presence of disturbances in the bioelectric activities of the central and peripheral nervous system in MG patients.
引用
收藏
页数:11
相关论文
共 38 条
[1]   Myasthenia gravis, atypical polyneuropathy and multiple autoimmune phenomena in the same patient, with HLA-immunogenetic profile expectable for Greek chronic inflammatory demyelinating polyneuropathy: a case report [J].
Anagnostouli, Maria ;
Vakrakou, Aigli G. ;
Zambelis, Thomas ;
Boufidou, Fotini ;
Nikolaou, Chrysoula ;
Karandreas, Nikolaos ;
Kilidireas, Constantinos .
INTERNATIONAL JOURNAL OF NEUROSCIENCE, 2022, 132 (06) :593-600
[2]   SHORT-LATENCY SOMATOSENSORY EVOKED-POTENTIALS TO MEDIAN NERVE-STIMULATION IN PATIENTS WITH DIFFUSE NEUROLOGIC DISEASE [J].
ANZISKA, BJ ;
CRACCO, RQ .
NEUROLOGY, 1983, 33 (08) :989-993
[3]  
Asanuma K, 1999, Rinsho Shinkeigaku, V39, P739
[4]  
Baltz T, 2015, FRONT CELL NEUROSCI, V9, DOI [10.3339/fncel.2015.00272, 10.3389/fncel.2015.00272]
[5]  
Bieszczad M, 1995, Neurol Neurochir Pol, V29, P77
[6]   Autoimmune Pathology in Myasthenia Gravis Disease Subtypes Is Governed by Divergent Mechanisms of Immunopathology [J].
Fichtner, Miriam L. ;
Jiang, Ruoyi ;
Bourke, Aoibh ;
Nowak, Richard J. ;
O'Connor, Kevin C. .
FRONTIERS IN IMMUNOLOGY, 2020, 11
[7]  
Fotiou F, 1994, Electromyogr Clin Neurophysiol, V34, P171
[8]   Evidence for a central cholinergic deficit in myasthenia gravis [J].
Fotiou, F ;
Fountoulakis, KN .
JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES, 2000, 12 (04) :514-515
[9]   A CASE OF MYASTHENIA-GRAVIS ASSOCIATED WITH OPTIC NEURITIS [J].
GHEZZI, A ;
ZAFFARONI, M ;
CAPUTO, D ;
ZIBETTI, A ;
MARIANI, G .
JOURNAL OF NEUROLOGY, 1984, 231 (02) :94-95
[10]   MuSK IgG4 autoantibodies cause myasthenia gravis by inhibiting binding between MuSK and Lrp4 [J].
Huijbers, Maartje G. ;
Zhang, Wei ;
Klooster, Rinse ;
Niks, Erik H. ;
Friese, Matthew B. ;
Straasheijm, Kirsten R. ;
Thijssen, Peter E. ;
Vrolijk, Hans ;
Plomp, Jaap J. ;
Vogels, Pauline ;
Losen, Mario ;
Van der Maarel, Silvere M. ;
Burden, Steven J. ;
Verschuuren, Jan J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (51) :20783-20788