ELECTROPHYSIOLOGICAL TESTING IS CORRELATED WITH MYASTHENIA GRAVIS SEVERITY

被引:27
作者
Abraham, Alon [1 ]
Breiner, Ari [1 ]
Barnett, Carolina [1 ]
Katzberg, Hans D. [1 ]
Lovblom, Leif E. [2 ,3 ]
Ngo, Mylan [1 ]
Bril, Vera [1 ]
机构
[1] Univ Toronto, Toronto Gen Hosp, Ellen & Martin Prosserman Ctr Neuromuscular Dis, Univ Hlth Network,Div Neurol,Dept Med, 200 Elizabeth St,Room 5 EB 309, Toronto, ON M5G 2C4, Canada
[2] Univ Toronto, Mt Sinai Hosp, Dept Med, Div Endocrinol & Metab, Toronto, ON, Canada
[3] Univ Toronto, Lunenfeld Tanenbaum Res Inst, Toronto, ON, Canada
关键词
disease severity; myasthenia gravis; optimal thresholds; QMGS; repetitive nerve stimulation; single fiber EMG; DOUBLE-BLIND; RELIABILITY;
D O I
10.1002/mus.25539
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Electrophysiological studies play an important role in the diagnosis of myasthenia gravis (MG). The objectives of this study was to explore the correlation of jitter and decrement with various clinical symptoms and signs and disease severity. Methods: We performed a retrospective chart review of 75MG patients who attended the neuromuscular clinic from April 2013 to May 2014. We compared clinical characteristics between patients with high jitter (> 100 mu s) and decrement (> 10%), and patients with lower values to explore the correlations and optimal thresholds of jitter and decrement for different clinical features. Results: High jitter and decrement values were associated with more severe disease, manifested by more frequent symptomatic bulbar and limb muscle weakness, more frequent ocular and limb muscle weakness on examination, higher quantitative MG score, and generalized disease. Conclusions: The yield of the electrophysiological assessment in MG extends beyond disease diagnosis and correlates with disease severity and the presence of generalized disease.
引用
收藏
页码:445 / 448
页数:4
相关论文
共 15 条
[1]  
AAEM Quality Assurance Comm, 2001, MUSCLE NERVE, V24, P1239
[2]  
Abraham A, 2016, MUSCLE NERVE
[3]   Repetitive nerve stimulation cutoff values for the diagnosis of myasthenia gravis [J].
Abraham, Alon ;
Alabdali, Majed ;
Alsulaiman, Abdulla ;
Breiner, Ari ;
Barnett, Carolina ;
Katzberg, Hans D. ;
Lovblom, Leif E. ;
Bril, Vera .
MUSCLE & NERVE, 2017, 55 (02) :166-170
[4]   Development and validation of the Myasthenia Gravis Impairment Index [J].
Barnett, Carolina ;
Bril, Vera ;
Kapral, Moira ;
Kulkarni, Abhaya ;
Davis, Aileen M. .
NEUROLOGY, 2016, 87 (09) :879-886
[5]  
Barnett Carolina, 2012, J Clin Neuromuscul Dis, V13, P201, DOI 10.1097/CND.0b013e31824619d5
[6]   Reliability testing of the quantitative myasthenia gravis score [J].
Barohn, RJ ;
McIntire, D ;
Herbelin, L ;
Wolfe, GI ;
Nations, S ;
Bryan, WW .
MYASTHENIA GRAVIS AND RELATED DISEASES: DISORDERS OF THE NEUROMUSCULAR JUNCTION, 1998, 841 :769-772
[7]  
Baruca M, 2016, MUSCLE NERVE
[8]   AAEM CASE-REPORT 3 - MYASTHENIA-GRAVIS [J].
JABLECKI, CK .
MUSCLE & NERVE, 1991, 14 (05) :391-397
[9]   Myasthenia gravis - Recommendations for clinical research standards [J].
Jaretzki, A ;
Barohn, RJ ;
Ernstoff, RM ;
Kaminski, HJ ;
Keesey, JC ;
Penn, AS ;
Sanders, DB .
NEUROLOGY, 2000, 55 (01) :16-23
[10]  
Katzberg Hans D, 2005, J Clin Neuromuscul Dis, V6, P109, DOI 10.1097/01.cnd.0000155026.66153.f0