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. 2021 Jul 22;13(8):1427.
doi: 10.3390/v13081427.

Neurodevelopment in Children Exposed to Zika Virus: What Are the Consequences for Children Who Do Not Present with Microcephaly at Birth?

Paula Fabiana Sobral da Silva  1   2 , Sophie Helena Eickmann  3 , Ricardo Arraes de Alencar Ximenes  1 , Celina Maria Turchi Martelli  4 , Elizabeth B Brickley  5 , Marília C Lima  3 , Ulisses R Montarroyos  1 , Maria Durce Costa Gomes de Carvalho  1   2 , Laura Cunha Rodrigues  5 , Thalia Velho Barreto de Araújo  6 , Liana O Ventura  7 , Danielle Maria da Silva Oliveira  1 , Regina Coeli Ferreira Ramos  8 , Demócrito de Barros Miranda-Filho  1 , On Behalf Of The Microcephaly Epidemic Research Group Merg
Affiliations

Neurodevelopment in Children Exposed to Zika Virus: What Are the Consequences for Children Who Do Not Present with Microcephaly at Birth?

Paula Fabiana Sobral da Silva et al. Viruses. .

Abstract

The relation of Zika virus (ZIKV) with microcephaly is well established. However, knowledge is lacking on later developmental outcomes in children with evidence of maternal ZIKV infection during pregnancy born without microcephaly. The objective of this analysis is to investigate the impact of prenatal exposure to ZIKV on neuropsychomotor development in children without microcephaly. We evaluated 274 children including 235 ZIKV exposed and 39 controls using the Bayley-III Scales of Infant and Toddler Development (BSIDIII) and neurological examination. We observed a difference in cognition with a borderline p-value (p = 0.052): 9.4% of exposed children and none of the unexposed control group had mild to moderate delays. The prevalence of delays in the language and motor domains did not differ significantly between ZIKV-exposed and unexposed children (language: 12.3% versus 12.8%; motor: 4.7% versus 2.6%). Notably, neurological examination results were predictive of neurodevelopmental delays in the BSIDIII assessments for exposed children: 46.7% of children with abnormalities on clinical neurological examination presented with delay in contrast to 17.8% among exposed children without apparent neurological abnormalities (p = 0.001). Overall, our findings suggest that relative to their unexposed peers, ZIKV-exposed children without microcephaly are not at considerably increased risk of neurodevelopmental impairment in the first 42 months of life, although a small group of children demonstrated higher frequencies of cognitive delay. It is important to highlight that in the group of exposed children, an abnormal neuroclinical examination may be a predictor of developmental delay. The article contributes to practical guidance and advances our knowledge about congenital Zika.

Keywords: Bayley scales; child development; congenital Zika; neuroclinical examination; paediatric cohort.

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Conflict of interest statement

The authors declare no conflict of interest.

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