Changes in electrophysiological findings of spinal muscular atrophy type I after the administration of nusinersen and onasemnogene abeparvovec: two case reports

被引:0
作者
Mizuno, Tomoko [1 ]
Kanouchi, Tadashi [2 ]
Tamura, Yumie [1 ]
Hirata, Ko [1 ]
Emoto, Runa [1 ]
Suzuki, Tomonori [1 ]
Kashimada, Kenichi [1 ]
Morio, Tomohiro [1 ]
机构
[1] Tokyo Med & Dent Univ, Dept Pediat & Dev Biol, 1-5-45 Yushima,Bunkyo Ku, Tokyo 1138519, Japan
[2] Tokyo Med & Dent Univ, Dept Lab Med, 1-5-45 Yushima,Bunkyo Ku, Tokyo 1138519, Japan
关键词
Spinal muscular atrophy; Nusinersen; Onasemnogene abeparvovec; Nerve conduction study; Needle electromyography; SMN2 COPY NUMBER; SMA;
D O I
10.1186/s12883-023-03420-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundRecently, there have been significant advances in the treatment of spinal muscular atrophy (SMA). Although clinical improvement in patients with SMA after the treatment has been reported, changes in electrophysiological findings, especially needle electromyography (EMG), have rarely been reported. Herein, we report the posttreatment changes in EMG and nerve conduction study findings over time in two patients with SMA type I.Case presentationPatient 1: A 2.5-year-old girl was diagnosed with SMA type I at 1 month of age. She received nusinersen four times and onasemnogene abeparvovec (OA) was administered at 6 months of age. The compound muscle action potential (CMAP) amplitudes of the median and tibial nerves increased over time. The needle EMG after the treatment showed high-amplitude motor unit potentials (MUPs) suggestive of reinnervation during voluntary contraction, which were not seen before the treatment. However, fibrillation potentials at rest were still seen after the treatment. Patient 2: A 2-year-old girl was diagnosed with SMA type I at 6 months of age. She had received nusinersen two times and OA was administered at 7 months of age. The CMAP amplitudes and the MUPs presented similar changes as presented in Case 1.ConclusionThis is the first report on the changes in needle EMG findings after treatment in patients with SMA type I. These findings suggested that peripheral nerve reinnervation occurred after the treatment, although active denervation was still present. The accumulation of these findings will be important for evaluating the effectiveness of treatment for SMA in the future.
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共 16 条
[1]   AVXS-101 (Onasemnogene Abeparvovec) for SMA 1: Comparative Study with a Prospective Natural History Cohort [J].
Al-Zaidy, Samiah A. ;
Kolb, Stephen J. ;
Lowes, Linda ;
Alfano, Lindsay N. ;
Shell, Richard ;
Church, Kathleen R. ;
Nagendran, Sukumar ;
Sproule, Douglas M. ;
Feltner, Douglas E. ;
Wells, Courtney ;
Ogrinc, Francis ;
Menier, Melissa ;
L'Italien, James ;
Arnold, W. David ;
Kissel, John T. ;
Kaspar, Brian K. ;
Mendell, Jerry R. .
JOURNAL OF NEUROMUSCULAR DISEASES, 2019, 6 (03) :307-317
[2]   SPINAL MUSCULAR ATROPHY: DIAGNOSIS AND MANAGEMENT IN A NEW THERAPEUTIC ERA [J].
Arnold, W. David ;
Kassar, Darine ;
Kissel, John T. .
MUSCLE & NERVE, 2015, 51 (02) :157-167
[3]   Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported cases [J].
Calucho, Maite ;
Bernal, Sara ;
Alias, Laura ;
March, Francesca ;
Vencesla, Adoracion ;
Rodriguez-Alvarez, Francisco J. ;
Aller, Elena ;
Fernandez, Raquel M. ;
Borrego, Salud ;
Milian, Jose M. ;
Hernandez-Chico, Concepcion ;
Cusco, Ivon ;
Fuentes-Prior, Pablo ;
Tizzano, Eduardo F. .
NEUROMUSCULAR DISORDERS, 2018, 28 (03) :208-215
[4]   Spinal muscular atrophy [J].
D'Amico, Adele ;
Mercuri, Eugenio ;
Tiziano, Francesco D. ;
Bertini, Enrico .
ORPHANET JOURNAL OF RARE DISEASES, 2011, 6
[5]   Risdiplam-Treated Infants with Type 1 Spinal Muscular Atrophy versus Historical Controls [J].
Darras, Basil T. ;
Masson, Riccardo ;
Mazurkiewicz-Beldzinska, Maria ;
Rose, Kristy ;
Xiong, Hui ;
Zanoteli, Edmar ;
Baranello, Giovanni ;
Bruno, Claudio ;
Vlodavets, Dmitry ;
Wang, Yi ;
El-Khairi, Muna ;
Gerber, Marianne ;
Gorni, Ksenija ;
Khwaja, Omar ;
Kletzl, Heidemarie ;
Scalco, Renata S. ;
Fontoura, Paulo ;
Servais, Laurent .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 385 (05) :427-435
[6]   Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy [J].
Finkel, R. S. ;
Mercuri, E. ;
Darras, B. T. ;
Connolly, A. M. ;
Kuntz, N. L. ;
Kirschner, J. ;
Chiriboga, C. A. ;
Saito, K. ;
Servais, L. ;
Tizzano, E. ;
Topaloglu, H. ;
Tulinius, M. ;
Montes, J. ;
Glanzman, A. M. ;
Bishop, K. ;
Zhong, Z. J. ;
Gheuens, S. ;
Bennett, C. F. ;
Schneider, E. ;
Farwell, W. ;
De Vivo, D. C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 377 (18) :1723-1732
[7]   Motor unit changes in children with symptomatic spinal muscular atrophy treated with nusinersen [J].
Kariyawasam, Didu ;
D'Silva, Arlene ;
Howells, James ;
Herbert, Karen ;
Geelan-Small, Peter ;
Lin, Cindy Shin-Yi ;
Farrar, Michelle Anne .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2021, 92 (01) :78-85
[8]   IDENTIFICATION AND CHARACTERIZATION OF A SPINAL MUSCULAR ATROPHY-DETERMINING GENE [J].
LEFEBVRE, S ;
BURGLEN, L ;
REBOULLET, S ;
CLERMONT, O ;
BURLET, P ;
VIOLLET, L ;
BENICHOU, B ;
CRUAUD, C ;
MILLASSEAU, P ;
ZEVIANI, M ;
LEPASLIER, D ;
FREZAL, J ;
COHEN, D ;
WEISSENBACH, J ;
MUNNICH, A ;
MELKI, J .
CELL, 1995, 80 (01) :155-165
[9]  
McDonald CM, Musculoskeletal Key
[10]   Five-Year Extension Results of the Phase 1 START Trial of Onasemnogene Abeparvovec in Spinal Muscular Atrophy [J].
Mendell, Jerry R. ;
Al-Zaidy, Samiah A. ;
Lehman, Kelly J. ;
McColly, Markus ;
Lowes, Linda P. ;
Alfano, Lindsay N. ;
Reash, Natalie F. ;
Iammarino, Megan A. ;
Church, Kathleen R. ;
Kleyn, Aaron ;
Meriggioli, Matthew N. ;
Shell, Richard .
JAMA NEUROLOGY, 2021, 78 (07) :834-841