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Quantified Assessment of Infant's Gross Motor Abilities Using a Multisensor Wearable
Published on: May 17, 2024
General movements in early infancy predict neuromotor development at 9 to 12 years of age
Sabina E Groen1, Alida C E de Blécourt, Klaas Postema
1Centre of Rehabilitation, University Medical Center, University of Groningen, Groningen, The Netherlands.
Insights
Assessing general movements (GMs) in infancy, particularly fidgety GMs, can predict minor neurological dysfunction (MND) in children. Abnormal fidgety GMs correlate with coordination and fine motor issues later in life.
Area of Science:
- Developmental neuroscience
- Pediatric neurology
- Movement analysis
Background:
- General movements (GMs) assessment in infancy is crucial for predicting cerebral palsy (CP).
- The predictive value of GMs for minor neurological dysfunction (MND) requires further investigation.
Purpose of the Study:
- To explore the utility of GM assessment in predicting MND at 9 to 12 years of age.
- To determine if infant GM quality relates to long-term neurological outcomes beyond CP.
Main Methods:
- Prospective study of low-risk and high-risk infants.
- Assessment of general movements (GMs) quality at 'writhing' and 'fidgety' GM periods.
- Follow-up neurological assessment at 9 to 12 years for children without CP.
Main Results:
- GM quality at 'fidgety age' correlated with neurological condition (MND) at follow-up (rho=0.46, p<0.01).
- Abnormal fidgety GMs specifically predicted coordination problems (chi2=6.1, p=0.01) and fine manipulative disability (p<0.05).
Conclusions:
- Infant GM quality, especially during the fidgety period, provides valuable information on the integrity of supraspinal pathways.
- GM assessment can predict subtle neurological deficits, including MND, in later childhood.
Abstract:
Assessment of the quality of general movements (GMs) in early infancy is a powerful instrument to predict cerebral palsy (CP). The aim of the present study is to explore the value of GM assessment in predicting minor neurological dysfunction (MND) at 9 to 12 years of age. Two groups of infants were studied prospectively: 28 low-risk full-term infants (11 females, 17 males) and 24 high-risk infants, mostly born preterm (<37 weeks; 11 females, 13 males). In each group the quality of GMs (normal or abnormal) was assessed during two developmental periods: the age at which 'writhing' GMs occur (36 weeks' postmenstrual age to 7 weeks' postterm) and the age at which 'fidgety' GMs occur (8 to 17 weeks' postterm). Eight of 24 high-risk infants were diagnosed as having CP at 4 to 9 years of age. The remaining 44 children were followed-up at 9 to 12 years. In children without CP, quality of GMs at 'fidgety age' was related to neurological condition (normal, simple MND, complex MND) at follow-up (rho=0.46, p<0.01). Abnormal GMs at 'fidgety-GM age' showed a specific relationship to the development of coordination problems (chi2=6.1, p=0.01) and fine manipulative disability (Fisher, p<0.05) at 9 to 12 years. This finding supports the notion that the quality of GMs may provide information on the integrity of complex supraspinal circuitries.
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