# Respiratory effects of nusinersen treatment in pediatric patients with spinal muscular atrophy types 2 and 3

**Authors:** Mika Rochman, Dar Shay Levanon, Israel Amirav, Moria Be’er, Michal Cahal, Omri Besor, Aviva Fattal-Valevski, Moran Lavie

PMC · DOI: 10.1007/s00431-025-06475-0 · European Journal of Pediatrics · 2025-10-20

## TL;DR

This study finds that nusinersen treatment may help preserve respiratory muscle strength in children with spinal muscular atrophy types 2 and 3, despite some decline in lung capacity.

## Contribution

Nusinersen may preserve respiratory muscle strength in SMA patients with types 2 and 3.

## Key findings

- Nusinersen treatment was associated with stable or improved respiratory muscle strength parameters like peak cough flow and maximal voluntary ventilation.
- The need for non-invasive ventilation and mechanical insufflation-exsufflation increased over three years of treatment.
- Body mass index remained stable, and all patients maintained oral intake during treatment.

## Abstract

Spinal muscular atrophy (SMA) is a progressive neuromuscular disorder characterized by respiratory decline. While nusinersen improves motor function, its long-term respiratory effects in milder SMA types (2 and 3) remain unclear. This study evaluates pulmonary outcomes following 3 years of treatment. We retrospectively reviewed genetically confirmed SMA 2 and 3 pediatric patients treated with nusinersen (2017–2022). Data included demographics, non-invasive ventilation (NIV) and mechanical insufflation-exsufflation (MIE) use, body mass index (BMI), feeding method, scoliosis, and respiratory hospitalizations. Pulmonary function tests (PFTs) at baseline and at year 3 included percent-predicted forced vital capacity (ppFVC), FEV1/FVC ratio, peak cough flow (PCF), maximal voluntary ventilation (MVV), maximal inspiratory pressure (MIP), and maximal expiratory pressure (MEP). Included were 15 patients with type 2 and 13 patients with type 3 SMA. Their mean age at diagnosis was 3.5 ± 4 years and 13.8 ± 5.4 years at nusinersen initiation. One was lost to follow-up. At baseline, 6 patients used NIV and 8 used MIE. After 3 years, NIV use increased to 7/27 and MIE to 14/27. All 27 patients maintained oral intake and their BMI remained stable. ppFVC declined, most notably in year 3 (− 13.5%, p < 0.001). PCF, MVV, MIP, and MEP values remained stable or mildly improved, suggesting a slower decline or relative stabilization compared to natural progression.

Conclusion: Nusinersen may help preserve respiratory muscle strength and delay the need for ventilatory support among pediatric patients with SMA types 2 and 3. Although ppFVC declined, stability in other parameters supports a potential respiratory benefit.
What is Known:• SMA causes progressive respiratory decline over time.What is New:• Nusinersen may preserve respiratory muscle strength in SMA.

What is Known:

• SMA causes progressive respiratory decline over time.

What is New:

• Nusinersen may preserve respiratory muscle strength in SMA.

## Linked entities

- **Diseases:** spinal muscular atrophy (MONDO:0001516), SMA (MONDO:0019079)

## Full-text entities

- **Diseases:** SMA (MESH:D009134), neuromuscular disorder (MESH:D009468), cough (MESH:D003371), scoliosis (MESH:D012600), type 2 (MESH:D003924), SMA 2 and 3 (MESH:D014897)
- **Chemicals:** Nusinersen (MESH:C000590926)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12537763/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12537763/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12537763/full.md

---
Source: https://tomesphere.com/paper/PMC12537763