Development of new outcome measures for adult SMA type III and IV: a multimodal longitudinal study.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
May 2021
Historique:
received: 06 09 2020
accepted: 19 11 2020
revised: 19 11 2020
pubmed: 4 1 2021
medline: 22 6 2021
entrez: 3 1 2021
Statut: ppublish

Résumé

The aim of this study was the comprehensive characterisation of longitudinal clinical, electrophysiological and neuroimaging measures in type III and IV adult spinal muscular atrophy (SMA) with a view to propose objective monitoring markers for future clinical trials. Fourteen type III or IV SMA patients underwent standardised assessments including muscle strength testing, functional evaluation (SMAFRS and MFM), MUNIX (abductor pollicis brevis, APB; abductor digiti minimi, ADM; deltoid; tibialis anterior, TA; trapezius) and quantitative cervical spinal cord MRI to appraise segmental grey and white matter atrophy. Patients underwent a follow-up assessment with the same protocol 24 months later. Longitudinal comparisons were conducted using the Wilcoxon-test for matched data. Responsiveness was estimated using standardized response means (SRM) and a composite score was generated based on the three most significant variables. Significant functional decline was observed based on SMAFRS (p = 0.019), pinch and knee flexion strength (p = 0.030 and 0.027), MUNIX and MUSIX value in the ADM (p = 0.0006 and 0.043) and in TA muscle (p = 0.025). No significant differences were observed based on cervical MRI measures. A significant reduction was detected in the composite score (p = 0.0005, SRM = -1.52), which was the most responsive variable and required a smaller number of patients than single variables in the estimation of sample size for clinical trials. Quantitative strength testing, SMAFRS and MUNIX readily capture disease progression in adult SMA patients. Composite multimodal scores increase predictive value and may reduce sample size requirements in clinical trials.

Identifiants

pubmed: 33388927
doi: 10.1007/s00415-020-10332-5
pii: 10.1007/s00415-020-10332-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1792-1802

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Auteurs

Giorgia Querin (G)

Centre de Référence Maladies Neuromusculaires Paris-Est, APHP, Hôpital Pitié-Salpêtrière, Service de Neuromyologie, Paris, France.
Laboratoire D'Imagerie Biomédicale, Sorbonne Université, CNRS, INSERM, Paris, France.
Institut de Myologie, I-Motion Adultes Plateforme, Paris, France.

Timothée Lenglet (T)

Département de Neurophysiologie, APHP, Hôpital Pitié-Salpêtrière, Paris, France.
APHP, Centre Référant SLA, Hôpital Pitié-Salpêtrière, Paris, France.

Rabab Debs (R)

Département de Neurophysiologie, APHP, Hôpital Pitié-Salpêtrière, Paris, France.

Tanya Stojkovic (T)

Centre de Référence Maladies Neuromusculaires Paris-Est, APHP, Hôpital Pitié-Salpêtrière, Service de Neuromyologie, Paris, France.

Anthony Behin (A)

Centre de Référence Maladies Neuromusculaires Paris-Est, APHP, Hôpital Pitié-Salpêtrière, Service de Neuromyologie, Paris, France.

François Salachas (F)

APHP, Centre Référant SLA, Hôpital Pitié-Salpêtrière, Paris, France.

Nadine Le Forestier (N)

APHP, Centre Référant SLA, Hôpital Pitié-Salpêtrière, Paris, France.
Département de Recherche en Éthique, EA 1610: Etudes Des Sciences Et Techniques, Université Paris Sud/Paris Saclay, Paris, France.

Maria Del Mar Amador (MDM)

APHP, Centre Référant SLA, Hôpital Pitié-Salpêtrière, Paris, France.

Gaëlle Bruneteau (G)

APHP, Centre Référant SLA, Hôpital Pitié-Salpêtrière, Paris, France.

Pascal Laforêt (P)

Neurology Department, Nord/Est/Ile de France Neuromuscular Center, Raymond-Poincaré Hospital, Garches, France.
INSERM U1179, END-ICAP, Versailles Saint-Quentin-en-Yvelines University, Montigny-le-Bretonneux, France.

Sophie Blancho (S)

Institut Pour La Recherche Sur La Moelle Epinière Et L'Encéphale (IRME), Paris, France.

Véronique Marchand-Pauvert (V)

Laboratoire D'Imagerie Biomédicale, Sorbonne Université, CNRS, INSERM, Paris, France.

Peter Bede (P)

Laboratoire D'Imagerie Biomédicale, Sorbonne Université, CNRS, INSERM, Paris, France.
APHP, Centre Référant SLA, Hôpital Pitié-Salpêtrière, Paris, France.
Computational Neuroimaging Group, Academic Unit of Neurology, Trinity College, Dublin, Ireland.

Jean-Yves Hogrel (JY)

Institute of Myology, Neuromuscular Investigation Center, Paris, France.

Pierre-François Pradat (PF)

Laboratoire D'Imagerie Biomédicale, Sorbonne Université, CNRS, INSERM, Paris, France. pierre-francois.pradat@aphp.fr.
APHP, Centre Référant SLA, Hôpital Pitié-Salpêtrière, Paris, France. pierre-francois.pradat@aphp.fr.
Northern Ireland Centre for Stratified Medicine, Biomedical Sciences Research Institute Ulster University, Altnagelvin Hospital, Derry/Londonderry, C-TRIC, UK. pierre-francois.pradat@aphp.fr.
Département de Neurologie, 47 Boulevard de l'sHôpital, 75634, Paris cedex 13, France. pierre-francois.pradat@aphp.fr.

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