Effect of nusinersen on motor, respiratory and bulbar function in early-onset spinal muscular atrophy

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Albert-Ludwigs-Universität Freiburg
  • Kaiser Franz Josef Krankenhaus
  • Universität Duisburg-Essen
  • Deutsche Gesellschaft für Muskelkranke (DGM) e.V.
  • Ludwig-Maximilians-Universität München (LMU)
  • Medizinische Universität Innsbruck
  • Ordensklinikum Linz
  • Technische Universität München
  • Kepler Universitätsklinikum
  • Universität des Saarlandes
  • Justus-Liebig-Universität Gießen
  • Eberhard Karls Universität Tübingen
  • Friedrich-Schiller-Universität Jena
  • Medizinische Hochschule Hannover (MHH)
  • Universität Hamburg
  • Ruhr-Universität Bochum
  • Universitätsklinikum Würzburg
  • German Red Cross
  • Landeskrankenhaus Bregenz
  • Klinikum Kassel GmbH
  • Westfälische Wilhelms-Universität Münster
  • Klinikum Wels - Grieskirchen GmbH
  • LK-Banden-Mödling
  • Friedrich-Alexander-Universität Erlangen-Nürnberg
  • Charité – Universitätsmedizin Berlin
  • Asklepios Klinik Hamburg Nord-Heidberg
  • Universität Heidelberg
  • University of Ottawa
  • Universität Bonn

Abstract

5q-associated spinal muscular atrophy is a rare neuromuscular disorder with the leading symptom of a proximal muscle weakness. Three different drugs have been approved by the European Medicines Agency and Food and Drug Administration for the treatment of spinal muscular atrophy patients, however, long-term experience is still scarce. In contrast to clinical trial data with restricted patient populations and short observation periods, we report here real-world evidence on a broad spectrum of patients with early-onset spinal muscular atrophy treated with nusinersen focusing on effects regarding motor milestones, and respiratory and bulbar insufficiency during the first years of treatment. Within the SMArtCARE registry, all patients under treatment with nusinersen who never had the ability to sit independently before the start of treatment were identified for data analysis. The primary outcome of this analysis was the change in motor function evaluated with the Children’s Hospital of Philadelphia Infant Test of Neuromuscular Disorders and motor milestones considering World Health Organization criteria. Further, we evaluated data on the need for ventilator support and tube feeding, and mortality. In total, 143 patients with early-onset spinal muscular atrophy were included in the data analysis with a follow-up period of up to 38 months. We observed major improvements in motor function evaluated with the Children’s Hospital of Philadelphia Infant Test of Neuromuscular Disorders. Improvements were greater in children >2 years of age at start of treatment than in older children. 24.5% of children gained the ability to sit independently. Major improvements were observed during the first 14 months of treatment. The need for intermittent ventilator support and tube feeding increased despite treatment with nusinersen. Our findings confirm the increasing real-world evidence that treatment with nusinersen has a dramatic influence on disease progression and survival in patients with early-onset spinal muscular atrophy. Major improvements in motor function are seen in children younger than 2 years at the start of treatment. Bulbar and respiratory function needs to be closely monitored, as these functions do not improve equivalent to motor function.

Details

OriginalspracheEnglisch
Seiten (von - bis)668-677
Seitenumfang10
FachzeitschriftBrain
Jahrgang146
Ausgabenummer2
PublikationsstatusVeröffentlicht - 13 Feb. 2023
Peer-Review-StatusJa

Externe IDs

PubMed 35857854

Schlagworte

ASJC Scopus Sachgebiete

Schlagwörter

  • SMA, motor function, motor milestones, nusinersen, spinal muscular atrophy, Injections, Spinal, Humans, Infant, Muscular Atrophy, Spinal/drug therapy, Spinal Muscular Atrophies of Childhood/drug therapy, Oligonucleotides/therapeutic use, Child

Bibliotheksschlagworte