Evidence map›Paper›PMID 41830094›Full record

ArticleJournal of neuromuscular diseases2026

Impairment of lip and tongue strength in symptomatic SMA1 patients: Results from a 4-center prospective study using the IOPI.

Charlotte Colot, Federica Trucco, Pablo Ruiz Chicaiza, Elke Everaert, Sarah Muys, Valentine Tahon, Linde Van Himme, Elke Devos, Arnaud Vanlander, Andrea Lizio and 8 more

Abstract read
In one paragraph

Article in Journal of neuromuscular diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

18 authors.

Charlotte ColotDepartment of Paediatric Neurology and Neuromuscular Reference Center, Hôpital Universitaire des Enfants Reine Fabiola (HUDERF)- Hôpital Universitaire de Bruxelles (HUB), Université Libre de Bruxelles (ULB), Brussels, Belgium.
Federica TruccoDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova; Paediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy.
Pablo Ruiz ChicaizaDepartment of Paediatric Neurology and Neuromuscular Reference Center, Hôpital Universitaire des Enfants Reine Fabiola (HUDERF)- Hôpital Universitaire de Bruxelles (HUB), Université Libre de Bruxelles (ULB), Brussels, Belgium.ORCID 0000-0003-2397-1240
Elke EveraertDepartment of Paediatric Neurology, Neuromuscular Reference Center (NMRC) Ghent University Hospital (UZ Gent), Ghent, Belgium.
Sarah MuysDepartment of Paediatric Neurology, Neuromuscular Reference Center (NMRC) Ghent University Hospital (UZ Gent), Ghent, Belgium.
Valentine TahonDepartment of Paediatric Neurology, Neuromuscular Reference Center (NMRC) Ghent University Hospital (UZ Gent), Ghent, Belgium.
Linde Van HimmeDepartment of Paediatric Neurology, Neuromuscular Reference Center (NMRC) Ghent University Hospital (UZ Gent), Ghent, Belgium.
Elke DevosDepartment of Paediatric Neurology, Neuromuscular Reference Center (NMRC) Ghent University Hospital (UZ Gent), Ghent, Belgium.
Arnaud VanlanderDepartment of Paediatric Neurology, Neuromuscular Reference Center (NMRC) Ghent University Hospital (UZ Gent), Ghent, Belgium.
Andrea LizioNeurorehabilitation Unit, The NeMo Clinical Center in Milan, University of Milan, Milan, Italy.
Francesca SalminNeurorehabilitation Unit, The NeMo Clinical Center in Milan, University of Milan, Milan, Italy.
Giorgia CorattiPediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Emilio AlbamonteNeurorehabilitation Unit, The NeMo Clinical Center in Milan, University of Milan, Milan, Italy.
Giulia StancaPediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Marika PanePediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Eugenio MercuriPediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Valeria SansoneDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova; Paediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy.
Nicolas DeconinckDepartment of Paediatric Neurology and Neuromuscular Reference Center, Hôpital Universitaire des Enfants Reine Fabiola (HUDERF)- Hôpital Universitaire de Bruxelles (HUB), Université Libre de Bruxelles (ULB), Brussels, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpinal muscular atrophy (SMA) is a genetic neuromuscular disease characterized by muscular atrophy and respiratory and bulbar dysfunction, especially in the most severe phenotypes (SMA type 0 and 1). Swallowing function remains understudied because assessment tools are often unavailable or poorly tolerated by young children. The Iowa Oral Performance Instrument (IOPI), that measures orofacial strength via a small air-filled bulb has recently been evaluated in SMA type 2 and 3 patients.

objectiveThe purpose of this study was to investigate muscle strength of several muscles used during the oral phase of swallowing using IOPI in SMA type 1 children treated with nusinersen compared to healthy controls. In addition, it sought to correlate labial and lingual pressures with known key predictors of phenotype severity (Children's Hospital Of Philadelphia Infant Test of Neuromuscular Disorders [CHOP INTEND], age at first symptoms,

methodsCombining results from four independent centers, we recruited 22 individuals with a confirmed genetic diagnosis of symptomatic SMA type 1. All patients had been treated with nusinersen for at least 2.5 years and had undergone at least one IOPI measurement at a median age of 5.4 years. IOPI data were compared to age- and gender-matched controls and published normative data when available.

resultsOral pressures were lower in patients than in typically developing children (lips:

conclusionsIOPI measurements objectively demonstrate orofacial weakness in this population compared with healthy controls and may serve as a biomarker to monitor the impact of comprehensive management, including disease-modifying therapies, on oral swallowing function in SMA type 1.

Indexed as

Neuromuscular diseaseoral pressuresorofacial weaknessspinal muscular atrophy type 1swallowing

Identifiers

PMID41830094
PMCPMC13438376

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.