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Neurodevelopmental Follow-Up in Children with Intrauterine and Perinatal Exposure to Chikungunya Virus
Fátima Cristiane Pinho de Almeida Di Maio Ferreira1, Karin Nielsen-Saines2, Maria Elisabeth Lopes Moreira3
1Department of Neonatal Intensive Care, Gaffrée and Guinle University Hospital, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.
Insights
Chikungunya virus (CHIKV) exposure during pregnancy can lead to neurodevelopmental issues in children, even if the mother or child isn't infected. Early infant neurodevelopment monitoring is crucial for children exposed to maternal CHIKV infection.
Area of Science:
- Neuroscience
- Virology
- Pediatrics
Background:
- Chikungunya virus (CHIKV) infection during pregnancy poses potential risks to fetal and infant neurodevelopment.
- Understanding the long-term neurological consequences of intrauterine and perinatal CHIKV exposure is critical for early intervention.
Purpose of the Study:
- To investigate the neurodevelopmental outcomes in infants and toddlers following intrauterine or perinatal exposure to chikungunya virus (CHIKV).
Main Methods:
- A cohort study in Brazil compared neurodevelopment in CHIKV-exposed children (n=60) with unexposed controls.
- Assessments included General Movement Assessments, Bayley-III Scales of Infant and Toddler Development, and the Modified Checklist for Autism in Toddlers.
- Developmental delay (DD) was defined as a Bayley score <70, and risk of DD as a score <85.
Main Results:
- CHIKV-exposed children showed significantly higher rates of developmental delay (20% vs 3%) and risk of developmental delay (29% motor, 23% cognitive) compared to controls.
- Language, motor, and cognitive domains were affected, with 23% of exposed children screening positive for autism spectrum disorder.
- Neurodevelopmental abnormalities were observed in both CHIKV-infected and uninfected exposed children.
Conclusions:
- Intrauterine or perinatal CHIKV exposure is associated with abnormal neurodevelopmental outcomes in infants and toddlers.
- Monitoring infant neurodevelopment is recommended for all pregnancies with CHIKV exposure to enable timely interventions.
- Early detection and intervention can help mitigate potential neurodevelopmental sequelae in affected children.
Objective:
To investigate the effects of intrauterine and perinatal exposure to chikungunya virus (CHIKV) on neurodevelopment in infants and toddlers.
Study Design:
We conducted a cohort study comparing children with intrauterine or perinatal exposure to maternal CHIKV infection with unexposed controls in Rio de Janeiro, Brazil. Neurodevelopment was assessed with General Movement Assessments in the first 6 months of life, and the Bayley-III Scales of Infant and Toddler Development and Modified Checklist for Autism in Toddlers for older children. Developmental delay (DD) was defined as a Bayley score less than 70 and risk of DD as a score less than 85.
Results:
Among 60 children exposed to intrauterine or perinatal CHIKV, 20 (33%) had laboratory confirmation of CHIKV infection by reverse transcription polymerase chain reaction or immunoglobulin M serology and 40 did not; 44 exposed children (15 infected and 29 uninfected) had General Movement Assessment performed, with 19% having suboptimal or abnormal results. At 11-42 months of age, 35 exposed children and 78 unexposed controls had Bayley-III assessments. Compared with controls, exposed children had higher rates of DD (7 [20%] vs 2 [3%], P = .004) driven by the language domain, and greater risk of DD driven by motor and cognitive domains scores (10 [29%] vs 10 [13%], P = .03 and 8 [23%] vs 5 [6%], P = .02, respectively). Eight of 35 (23%), CHIKV exposed children screened positive for autism spectrum disorder. CHIKV-exposed uninfected children had 2 (9.5%) cases of DD and 5 (23.8%) cases of autism spectrum disorder.
Conclusions:
Abnormal neurodevelopmental results were seen in both infected and uninfected children with intrauterine or perinatal CHIKV exposure. Infant neurodevelopment monitoring should be considered following exposure to maternal CHIKV infection in pregnancy to facilitate early interventions and to mitigate neurodevelopmental sequelae.
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