Key result
Spinal muscular atrophy is linked to markedly lower gait speed reserve compared to healthy controls.
Why the study?
Gait speed has not been explored in spinal muscular atrophy despite being a valid indicator of function and health in multiple populations.
Does gait speed correlate with strength and fatigability in ambulatory individuals with spinal muscular atrophy compared to healthy controls?
Observational (n=24)
Does gait speed correlate with strength and fatigability in ambulatory individuals with spinal muscular atrophy compared to healthy controls?
Standardized Mean Difference: 2.42
p-value: p=<0.001
Gait speed is diminished in spinal muscular atrophy and correlates with strength and fatigability, suggesting it may serve as a useful functional biomarker.
Hypothesis-generating for gait speed reserve as a biomarker in SMA; prospective studies needed to confirm longitudinal utility.
Introduction/Aims Gait Speed (GS), a valid and reliable indicator of function and health in multiple populations, has not been explored in spinal muscular atrophy (SMA). The purpose of this study was to characterize GS and gait speed reserves (GSR), and explore associations with strength and fatigability in SMA and healthy controls (HC). Methods Data were collected from ambulatory individuals with SMA ( n = 14) and controls (HC) ( n = 10). Using custom‐engineered instrumented insoles, stride velocity (SV) was collected during the Six‐Minute Walk Test (6MWT) and 10‐m walk/run (10MWR). Three GS variables were identified; SV50th Centile 6MWT (SV50C 6MWT ), 10MWR SV, and SV95th Centile 6MWT (SV95C 6MWT ). Gait speed reserve (GSR) was calculated from 10MWR and SV50C 6MWT . Repeated measures analysis of variance assessed differences in GS and GSR across groups. Spearman's Rho was used to assess associations between speed variables and clinical assessments. Results All speed variables were different within HC ( p < 0.001) and SMA ( p = 0.002). There was a significant Group × Speed interaction ( p < 0.001) with greater differences in HC. GSR was lower in SMA ( p < 0.001, d = 2.42). In SMA, thigh strength was associated with all three GS variables and inversely associated with fatigability ( p < 0.05). In HC, associations between GS and strength or fatigability were not observed. GSR was not associated with strength, fatigability, or GS in either group. Discussion GS is diminished in SMA and correlated with strength and fatigability. While reduced in SMA, GSR was not associated with GS, strength, or function. GS is a key vital sign of health and may be a useful biomarker in SMA.
No takes yet. Share an insight, caveat, or question.
Magun et al. (2026) conducted an observational in Spinal muscular atrophy (n=24). Spinal muscular atrophy vs. Healthy controls was evaluated on Gait speed reserve (GSR) (d = 2.42, p=<0.001). Spinal muscular atrophy was associated with significantly lower gait speed reserve compared to healthy controls (d = 2.42, p < 0.001), and gait speed correlated with thigh strength.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: