Longitudinal Assessment of 4-Year HFMSE Changes in SMA II and III Patients Treated With Nusinersen

Eur J Neurol. 2025 Jul;32(7):e70268. doi: 10.1111/ene.70268.

Abstract

Background: The aim of this international retrospective study was to assess 4-year change using the Hammersmith Functional Motor Scale Expanded (HFMSE) in individuals with type II and III spinal muscular atrophy (SMA) treated with nusinersen and to establish predictors of HFMSE changes.

Methods: Individuals with type II or III SMA, and at least 4 years of nusinersen-only treatment were included. All were assessed using the HFMSE. Age at baseline, sex, motor function, SMN2 copy number, and age of onset were also retrospectively collected. Linear mixed effect models were used to calculate yearly changes and trajectory predictors.

Results: We included 73 individuals with SMA type II (mean age 8.58 years, SD 7.91, IQR 3.04-10.70) and 111 type III (mean age 7.91 years, SD 17.83, IQR 8.15-34.42). Over 4 years, mean changes were + 4.18 (95% CI: 2.85-5.50) for SMA II and + 1.08 (95% CI: 0.12-2.04) for SMA III. Age (SMA II: -0.34\[-0.51 to -0.17]; SMA III: -0.13\[-0.20 to -0.06], p < 0.001) and baseline HFMSE (SMA II: 1.02\[0.70-1.34]; SMA III: 0.79\[0.71-0.87], p < 0.001) were the strongest predictors of progression, with younger age and higher baseline scores associated with better outcomes. Functional status was only predictive for type III (6.96\[4.26-9.66]).

Conclusion: Our results confirm that, given a follow up of 4 years, there is a persistent impact of nusinersen on clinical progression that is better observed in younger patients with higher HFMSE scores at baseline, especially during the first 2 years of treatment.

Keywords: Hammersmith functional motor scale expanded; long term results; motor function; nusinersen; spinal muscular atrophy.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Disease Progression
  • Female
  • Humans
  • Longitudinal Studies
  • Male
  • Oligonucleotides* / therapeutic use
  • Retrospective Studies
  • Severity of Illness Index
  • Spinal Muscular Atrophies of Childhood* / drug therapy
  • Spinal Muscular Atrophies of Childhood* / genetics
  • Spinal Muscular Atrophies of Childhood* / physiopathology
  • Survival of Motor Neuron 2 Protein / genetics
  • Treatment Outcome
  • Young Adult

Substances

  • nusinersen
  • Oligonucleotides
  • Survival of Motor Neuron 2 Protein