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Does nusinersen treatment rescue function of small motor units in symptomatic spinal muscular atrophy patients?
Over the last 5 years, three gene-targeting therapeutics have been approved for spinal muscular atrophy (SMA) including the splice switching oligonucleotide nusinersen in 2016, the gene therapy onasemnogene abepavovec in 2019 and the splice switching small molecule risdiplam in 2020. Although past and ongoing clinical trials demonstrate improvements in motor function scores in treated SMA patients of variable magnitude, the changes of motor neuron structure and function that underlie these clinical outcomes are unknown. In the paper by Kariyawasam et al1 this knowledge gap is explored in 20 children with symptomatic SMA of various types, who were treated with nusinersen for 1–2 years in the commercial setting and evaluated sequentially with a novel motor unit …
Contributors Both authors contributed equally to the conception, writing and editing of this editorial.
Funding The authors have declared a specific grant from a public funding agency.
Competing interests CJS has been a consultant to Biogen, Ionis Pharmaceuticals, Roche/Genetech, PTC Therapeutics, and AveXis Pharmaceuticals. CS receives grant support from Roche.
Patient consent for publication Not required.
Provenance and peer review Commissioned; internally peer reviewed.
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