Persistent neuromuscular junction transmission defects in adults with spinal muscular atrophy treated with nusinersen. Issue 2 (12th August 2021)

• Record Type: Journal Article
• Authors: Arnold, W David; Severyn, Steven; Zhao, Songzhu; Kline, David; Linsenmayer, Matthew; Kelly, Kristina; Tellez, Marco; Bartlett, Amy; Heintzman, Sarah; Reynolds, Jerry; Sterling, Gary; Weaver, Tristan; Rajneesh, Kiran; Burghes, Arthur H M; Kolb, Stephen J; Elsheikh, Bakri
• Is Part Of: BMJ neurology open. Volume 3:Issue 2(2021)
• Publication Date: 2021-08-12
• Subjects: spinal muscular atrophy -- neuromuscular -- EMG; Neurology -- Periodicals; 616.8
• DOI: 10.1136/bmjno-2021-000164
• Languages: English
• ISSNs: 2632-6140

Abstract

Abstract : Objective: Spinal muscular atrophy (SMA) is a motor neuron disease caused by low levels of survival motor neuron (SMN) protein. Prior work in models and patients has demonstrated electrophysiological and morphological defects at the neuromuscular junction (NMJ). Therapeutic development has resulted in clinically available therapies to increase SMN protein levels in patients and improve muscle function. Here we aimed to investigate the effect of SMN restoration (via nusinersen) on NMJ transmission in adults with SMA. Methods: Participants undergoing nusinersen treatment underwent 3 Hz repetitive nerve stimulation (RNS) of the spinal accessory nerve to assess compound muscle action potential amplitude decrement. Maximum voluntary isometric contraction (MVICT), Revised Upper Limb Module (RULM), and 6 min walk test (6MWT) were assessed for correlations with decrement. Results: Data from 13 ambulatory (7 men/6 women, mean age 40±11 years) and 11 non-ambulatory (3 men/8 women, mean age 38±12 years) participants were analysed. Cross-sectional analyses of RNS decrement were similar at 14 months of nusinersen (−14.2%±11.5%, n=17) vs baseline (−11.9%±8.3%, n=15) (unpaired t-test, p=0.5202). Longitudinal comparison of decrement in eight participants showed no change at 14 months (−13.9%±6.7%) vs baseline (−16.9%±13.4%) (paired t-test, p=0.5863). Decrement showed strong correlations with measures of MVICT, RULM and 6MWT but not age or disease duration. Conclusion: Adults with SMA had significant NMJ transmission defects that were not corrected with 14 months of nusinersen treatment. NMJ defects were negatively associated with physical function, and thus may represent a promising target for additive or combinatorial treatments.