Swallowing development in infants and toddlers with spinal muscular atrophy following therapy compared to healthy controls: the prospective controlled DySMA trial

Swallowing development is a crucial outcome measure for evaluating the effectiveness of disease-modifying therapies (DMT) in children with spinal muscular atrophy (SMA). However, data on this aspect remain limited due to a lack of assessment tools. This study aimed to evaluate swallowing development in infants and toddlers with SMA, compare it with healthy controls (HC), and investigate the influence of initial symptom status at start of DMT and SMN2 copy number. An observational study was conducted with infants and toddlers diagnosed with SMA at a single neuropediatric center and a HC group. Swallowing development was primarily assessed using the DySMA scale. Group differences and the impact of initial symptom status and SMN2 copy number on swallowing were analyzed using linear mixed-effects models. The study included 127 infants and toddlers, 35 with SMA (0–36 months, 19 girls), who started DMT either presymptomatically (n = 18) or symptomatically (n = 17), with two (n = 26) or three (n = 9) SMN2 copies, predominantly receiving Onasemnogene abeparvovec alone (n = 26), and a healthy control group (n = 92, 0–23 months, 34 girls). Children with SMA displayed significantly different swallowing development trajectories (-0.06 DySMA points by months of life, p=.06; 95% CI -0.13 to 0.01) compared to HC (+ 0.45 DySMA points by months of life, p<.01, 95% CI 0.25 to 0.65). Notably, those treated presymptomatically demonstrated swallowing progress comparable to HC up to 15–17 months but experienced a decline thereafter (18–24 months; β = 8.22, p<.001; 95% CI 4.20 to 12.26). The group with three SMN2 copies exhibited a developmental pattern similar to HC up to the age of 24 months. Higher SMN2 copy number and presymptomatic DMT initiation were associated with similar early swallowing development compared to HC. Long-term studies stratifying swallowing development by SMN2 copy number are warranted.

Authors

Institutions

Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2026-02-16
DOI
https://doi.org/10.1186/s13023-026-04227-3
Primary Topic
Neurogenetic and Muscular Disorders Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Swallowing development in infants and toddlers with spinal muscular atrophy following therapy compared to healthy controls: the prospective controlled DySMA trial

Jana Zang, J. Johannsen, Paula Steffens, Jonas Denecke et al.
Orphanet Journal of Rare Diseases
Neurogenetic and Muscular Disorders Research
article

Swallowing development in infants and toddlers with spinal muscular atrophy following therapy compared to healthy controls: the prospective controlled DySMA trial

Jana Zang, J. Johannsen, Paula Steffens, Jonas Denecke, Christina Pflug, Almut Nießen, Charlotte Dumitrascu, Deike Weiss, Julia Glinzer
article en

Abstract

Swallowing development is a crucial outcome measure for evaluating the effectiveness of disease-modifying therapies (DMT) in children with spinal muscular atrophy (SMA). However, data on this aspect remain limited due to a lack of assessment tools. This study aimed to evaluate swallowing development in infants and toddlers with SMA, compare it with healthy controls (HC), and investigate the influence of initial symptom status at start of DMT and SMN2 copy number. An observational study was conducted with infants and toddlers diagnosed with SMA at a single neuropediatric center and a HC group. Swallowing development was primarily assessed using the DySMA scale. Group differences and the impact of initial symptom status and SMN2 copy number on swallowing were analyzed using linear mixed-effects models. The study included 127 infants and toddlers, 35 with SMA (0–36 months, 19 girls), who started DMT either presymptomatically (n = 18) or symptomatically (n = 17), with two (n = 26) or three (n = 9) SMN2 copies, predominantly receiving Onasemnogene abeparvovec alone (n = 26), and a healthy control group (n = 92, 0–23 months, 34 girls). Children with SMA displayed significantly different swallowing development trajectories (-0.06 DySMA points by months of life, p=.06; 95% CI -0.13 to 0.01) compared to HC (+ 0.45 DySMA points by months of life, p<.01, 95% CI 0.25 to 0.65). Notably, those treated presymptomatically demonstrated swallowing progress comparable to HC up to 15–17 months but experienced a decline thereafter (18–24 months; β = 8.22, p<.001; 95% CI 4.20 to 12.26). The group with three SMN2 copies exhibited a developmental pattern similar to HC up to the age of 24 months. Higher SMN2 copy number and presymptomatic DMT initiation were associated with similar early swallowing development compared to HC. Long-term studies stratifying swallowing development by SMN2 copy number are warranted.

Orphanet Journal of Rare DiseasesVol. 21(1)
Universität Hamburg (DE), University Medical Center Hamburg-Eppendorf (DE), University of Lübeck (DE)
Openalex Percentile: Top 54%
Neurogenetic and Muscular Disorders Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.