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      Nusinersen in adult patients with spinal muscular atrophy : Observations from a single center

      , , , , ,
      Neurology
      Ovid Technologies (Wolters Kluwer Health)

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          Abstract

          Objective

          To report our experience with adult patients with spinal muscular atrophy (SMA), some of whom were treated with nusinersen.

          Methods

          We reviewed charts of adult patients with SMA seen in our neuromuscular clinic between 2017 and 2019 and noted their demographics, clinical characteristics, treatment, and side effects.

          Results

          Twenty-two patients were included. Nine had type 2 and 13 type 3 SMA. Median age was 36 years (range 20–71). Most could not walk unassisted. Ten patients had significant respiratory impairment necessitating ventilation and 2 had tracheostomy. Seventeen had severe scoliosis. Ten patients were treated with nusinersen for 6–24 months (median 12 months), 3 of whom required bone laminectomy for intrathecal access. One developed bowel and bladder incontinence following the procedure. In the treated group, on average, % Medical Research Council change was 2.5% at 12 months and 3.9% at 24 months. Most untreated patients remained stable; 3 had slightly declined. Five treated patients reported subjective improvement. Treatment side effects included post lumbar puncture headache in 5 patients, 2 of whom needed blood patch, and 1 bacterial meningitis requiring inpatient treatment. Three patients stopped treatment after 12–24 months due to lack of improvement, recurrent pneumonia, or proteinuria.

          Conclusion

          Side effects of nusinersen can be serious. Whereas half of treated patients reported modest improvement in function, there were no significant objective changes, which may point largely to a placebo effect.

          Classification of evidence

          This study provides Class IV evidence that for some adult patients with SMA, nusinersen improves subjective function and causes serious adverse effects.

          Related collections

          Most cited references6

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          Spinal muscular atrophy: clinical classification and disease heterogeneity.

          The clinical classification of spinal muscular atrophy, caused by deletion of the survival motor neuron 1 gene (SMN1), is based on age at onset and maximum function achieved. Evidence suggests that maximum function achieved is more closely related to life expectancy than age at onset. Therefore, it is important to wait for a period before assigning a patient to 1 of 5 classes of the disorder. Several diseases result from degeneration of the anterior horn cell but are not caused by SMN1. The classification for these conditions is evolving. This article offers an attempt at organizing one's thinking about this disease group.
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            Placebo effect of medication cost in Parkinson disease: a randomized double-blind study.

            To examine the effect of cost, a traditionally "inactive" trait of intervention, as contributor to the response to therapeutic interventions.
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              • Record: found
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              • Article: not found

              Evidence in focus: Nusinersen use in spinal muscular atrophy: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology.

              To identify the level of evidence for use of nusinersen to treat spinal muscular atrophy (SMA) and review clinical considerations regarding use.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Neurology
                Neurology
                Ovid Technologies (Wolters Kluwer Health)
                0028-3878
                1526-632X
                July 27 2020
                July 28 2020
                July 28 2020
                July 14 2020
                : 95
                : 4
                : e413-e416
                Article
                10.1212/WNL.0000000000009914
                32665408
                a48b320d-8a24-4bee-aeb2-283e25cf6f5f
                © 2020
                History

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