Key result
SMA non-sitters show a 5-point improvement in CHOP-INTEND motor function scores over 12 months.
Why the study?
Spinal muscular atrophy causes progressive muscular atrophy and weakness, prompting this study to analyse the effect of body parameters on motor function and fine motor skills over one year.
Does body mass index (BMI) affect motor function and fine motor skills in children with spinal muscular atrophy?
Observational (n=38)
No
Does body mass index (BMI) affect motor function and fine motor skills in children with spinal muscular atrophy?
Effect estimate: Mean score increase from 35 to 40 points (non-sitters, CHOP-INTEND)
Absolute Event Rate: 40% vs 35%
In patients with spinal muscular atrophy, increased BMI is associated with improved gross motor function, but may be associated with deteriorated fine motor skills in sitters.
Higher BMI associated with motor gains in SMA non-sitters; leaves open causality, fine-motor risks in sitters, and requires RCTs before nutritional practice change.
Spinal muscular atrophy mainly affects motor neurons in the spinal cord, leading to progressive muscular atrophy and weakness. This study aims to carefully analyse the effect of body parameters on motor function and fine motor skills, measured at one-year intervals, in patients with spinal muscular atrophy. The study included 38 participants diagnosed with SMA. Patients were divided into three groups based on their level of motor function: non-sitters (n = 9), sitters (n = 23), and walkers (n = 6). Anthropometric measurements (weight, height/length) were taken in all participants, and BMI and BMI-z-score were calculated. The motor function was assessed using validated scales: CHOP-INTEND for the non-sitters group and HFMSE scale for the sitters and walkers group. The RULM scale assessed fine motor skills for the sitters and walkers group. At the 12-month follow-up, the CHOP-INTEND scale showed improvement in most non-sitter patients (6/9). The sitter’s group was more heterogeneous on the HFMSE scale, with 10 out of 23 patients showing deterioration in function, 8 showing improvement, while the walker’s group showed the least variability. In the non-sitters group, the dominant category of BMI z-score was underweight, while half of the sitters in the group were underweight, although there were just as many healthy weights. The strongest group, the walkers, was mostly healthy. We have observed a certain tendency that as BMI increases, motor function increases in all groups, while fine motor skill decreases in the most varied sitters group. As BMI increases in SMA patients, motor function improves. Fine motor skill deteriorates as BMI increases in the sitter’s group. The assessment of individual components of motor function and fine motor skills reveals the actual changes that occur over time in patients with SMA.
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Gajewska et al. (2026) conducted an observational in Children aged 2-16 years with genetically confirmed spinal muscular atrophy types 1, 2, and 3 categorized by motor function level into non-sitters, sitters, and walkers (n=38). In children with SMA, motor function measured by CHOP-INTEND improved from 35 to 40 points over 12 months in the non-sitters group.
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