Heterogeneous development of children with Congenital Zika Syndrome-associated microcephaly
Juan P Aguilar Ticona1,2, Nivison Nery1,2, Simon Doss-Gollin3
1Instituto de Saúde Coletiva, Universidade Federal da Bahia, Salvador, BA, Brazil.
Insights
Children with Congenital Zika Syndrome (CZS) and microcephaly show significant developmental delays. Neurological exam scores, like the HINE, can predict cognitive and motor progress in these children.
Area of Science:
- Neurology
- Developmental Pediatrics
- Infectious Diseases
Background:
- Congenital Zika Syndrome (CZS) is linked to microcephaly, impacting neurological development.
- Long-term outcomes for children with CZS-associated microcephaly require further investigation beyond early childhood.
Purpose of the Study:
- To describe the neurological and neurodevelopmental outcomes of children with CZS-associated microcephaly beyond 2 years of age.
- To assess the correlation between neurological assessments and developmental progress in this cohort.
Main Methods:
- A longitudinal follow-up study of children with CZS-associated microcephaly in Salvador, Brazil.
- Neurological assessments using the Hammersmith Infant Neurological Examination (HINE) and neurodevelopmental assessments using the Bayley Scales of Infant and Toddler Neurodevelopment (Bayley-III).
Main Results:
- Severe developmental delay was identified in 97% of children assessed with Bayley-III.
- HINE scores correlated with Bayley-III cognitive and motor scores, indicating predictive value.
- Greater head circumference at follow-up was associated with higher cognitive and motor scores.
Conclusions:
- Children with CZS-associated microcephaly exhibit severe neurodevelopmental delays and heterogeneous profiles.
- HINE scores effectively capture neurological heterogeneity and predict cognitive and motor development.
- Neurological assessments are crucial for understanding long-term outcomes in CZS.
Objective:
To describe the neurological and neurodevelopmental outcomes of children with Congenital Zika Syndrome (CZS) associated microcephaly beyond 2 years of age.
Method:
We followed children with CZS-associated microcephaly in an outpatient clinic in Salvador, Brazil. Neurological and neurodevelopmental assessments were performed using the Hammersmith Infant Neurological Examination (HINE) and Bayley Scales of Infant and Toddler Neurodevelopment (Bayley-III) respectively.
Results:
Of the 42 children included, 19 were male (45.2%); median (interquartile range) age at neurological evaluation was 28 (25-32) months, and 36 (85.7%) had severe microcephaly. HINE and Bayley-III results were completed for 35/42 (83.3%) and 33/42 (78.5%) children respectively. Bayley-III identified a severe developmental delay in 32/33 (97.0%) children while 1/33 (3.0%) had only a mild delay. In the multivariable analysis, we found that Bayley-III and HINE scores were correlated. Better HINE scores were associated with higher Bayley-III cognitive raw scores (β = 0.29; CI 95% = 0.02-0.57) and motor raw scores (β = 0.43; CI 95% = 0.04-0.82) after adjusting for head circumference, prematurity, and age at neurodevelopmental evaluation. Furthermore, we found that greater head circumference at follow up was associated with higher cognitive (β = 1.27; CI 95% = 0.01-2.53) and motor raw scores (β = 2.03; CI 95% = 0.25-3.81).
Conclusion:
Children with CZS-associated microcephaly demonstrate severe neurodevelopmental delays and slower growth rates than their peers over time. Still, they have remarkably heterogeneous neurodevelopmental profiles according to neurological exam scores which correlate with their long-term outcomes. We found that HINE scores effectively captured the heterogeneity of neurological capabilities among these children and could be predictive of cognitive and motor development progress.
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