Neurodevelopment in normocephalic children with and without prenatal Zika virus exposure
Neurodevelopment in normocephalic children with and without prenatal Zika virus exposure
Objective: Zika virus (ZIKV) targets neural stem cells in the developing brain. However, the majority of ZIKV-exposed children are born without apparent neurological manifestations. It remains unclear if these children were protected from ZIKV neurotropism or if they harbour subtle pathology that is disruptive to brain development. We assess this by comparing neurodevelopmental outcomes in normocephalic ZIKV-exposed children relative to a parallel control group of unexposed controls.
Design: Cohort study.
Setting: Public health centres in Grenada, West Indies.
Patients: 384 mother–child pairs were enrolled during a period of active ZIKV transmission (April 2016–March 2017) and prospectively followed up to 30 months. Child exposure status was based on laboratory assessment of prenatal and postnatal maternal serum.
Main outcome measures: The INTERGROWTH-21st Neurodevelopment Assessment (INTER-NDA) package and Cardiff Vision Tests, administered and scored by research staff masked to child’s exposure status.
Results: A total of 131 normocephalic ZIKV exposed (n=68) and unexposed (n=63) children were assessed between 22 and 30 months of age. Approximately half of these children completed vision testing. There were no group differences in sociodemographics. Deficits in visual acuity (31%) and contrast sensitivity (23%) were apparent in the ZIKV-exposed infants in the absence of cognitive, motor, language or behavioural delays.
Conclusions: Overall neurodevelopment is likely to be unaffected in ZIKV-exposed children with normal head circumference at birth and normal head growth in the first 2 years of life. However, the visual system may be selectively vulnerable, which indicates the need for vision testing by 3 years of age.
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Blackmon, Karen
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Evans, Roberta
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Fernandes, Michelle
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Landon, Barbara
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Noël, Trevor
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Macpherson, Calum
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Cudjoe, Nikita
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Burgen, Kemi S.
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Punch, Bianca
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Krystosik, Amy
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Grossi-Soyster, Elysse N.
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LaBeaud, Angelle Desiree
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Waechter, Randall
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Blackmon, Karen
a0425a35-9dff-4420-b07b-9c3365babc69
Evans, Roberta
46ef2188-d0e1-447f-84ef-f79ac0208165
Fernandes, Michelle
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Landon, Barbara
74e43664-4060-4495-b4ef-a1992a5b9879
Noël, Trevor
bb87426c-b75e-4fc2-b8d2-f51f514cb89a
Macpherson, Calum
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Cudjoe, Nikita
39f0c11f-0d63-422a-ad43-67c7845fcfd4
Burgen, Kemi S.
c27894c1-2be4-4629-8d73-7b80a06fa0ba
Punch, Bianca
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Krystosik, Amy
8786f4a5-afb3-49d3-bd99-74126a48272c
Grossi-Soyster, Elysse N.
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LaBeaud, Angelle Desiree
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Waechter, Randall
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Blackmon, Karen, Evans, Roberta, Fernandes, Michelle, Landon, Barbara, Noël, Trevor, Macpherson, Calum, Cudjoe, Nikita, Burgen, Kemi S., Punch, Bianca, Krystosik, Amy, Grossi-Soyster, Elysse N., LaBeaud, Angelle Desiree and Waechter, Randall
(2021)
Neurodevelopment in normocephalic children with and without prenatal Zika virus exposure.
Archives of Disease in Childhood, 107, .
(doi:10.1136/archdischild-2020-321031).
Abstract
Objective: Zika virus (ZIKV) targets neural stem cells in the developing brain. However, the majority of ZIKV-exposed children are born without apparent neurological manifestations. It remains unclear if these children were protected from ZIKV neurotropism or if they harbour subtle pathology that is disruptive to brain development. We assess this by comparing neurodevelopmental outcomes in normocephalic ZIKV-exposed children relative to a parallel control group of unexposed controls.
Design: Cohort study.
Setting: Public health centres in Grenada, West Indies.
Patients: 384 mother–child pairs were enrolled during a period of active ZIKV transmission (April 2016–March 2017) and prospectively followed up to 30 months. Child exposure status was based on laboratory assessment of prenatal and postnatal maternal serum.
Main outcome measures: The INTERGROWTH-21st Neurodevelopment Assessment (INTER-NDA) package and Cardiff Vision Tests, administered and scored by research staff masked to child’s exposure status.
Results: A total of 131 normocephalic ZIKV exposed (n=68) and unexposed (n=63) children were assessed between 22 and 30 months of age. Approximately half of these children completed vision testing. There were no group differences in sociodemographics. Deficits in visual acuity (31%) and contrast sensitivity (23%) were apparent in the ZIKV-exposed infants in the absence of cognitive, motor, language or behavioural delays.
Conclusions: Overall neurodevelopment is likely to be unaffected in ZIKV-exposed children with normal head circumference at birth and normal head growth in the first 2 years of life. However, the visual system may be selectively vulnerable, which indicates the need for vision testing by 3 years of age.
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Submitted date: 25 October 2020
Accepted/In Press date: 10 August 2021
e-pub ahead of print date: 3 September 2021
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Local EPrints ID: 457179
URI: http://eprints.soton.ac.uk/id/eprint/457179
ISSN: 0003-9888
PURE UUID: f18d0265-da94-4bc0-8f82-bd67aacc29a8
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Date deposited: 25 May 2022 17:10
Last modified: 17 Mar 2024 04:10
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Contributors
Author:
Karen Blackmon
Author:
Roberta Evans
Author:
Michelle Fernandes
Author:
Barbara Landon
Author:
Trevor Noël
Author:
Calum Macpherson
Author:
Nikita Cudjoe
Author:
Kemi S. Burgen
Author:
Bianca Punch
Author:
Amy Krystosik
Author:
Elysse N. Grossi-Soyster
Author:
Angelle Desiree LaBeaud
Author:
Randall Waechter
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