Does Intra-Uterine Exposure to the Zika Virus Increase Risks of Cognitive Delay at Preschool Ages? Findings from a Zika-Exposed Cohort from Grenada, West Indies

Author:

Fernandes Michelle1234ORCID,Evans Roberta4ORCID,Cheng Mira5ORCID,Landon Barbara4,Noël Trevor4,Macpherson Calum4,Cudjoe Nikita4,Burgen Kemi S.4,Waechter Randall46ORCID,LaBeaud A. Desiree45,Blackmon Karen7ORCID

Affiliation:

1. MRC Lifecourse Epidemiology Centre, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK

2. Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK

3. Nuffield Department of Women’s Productive Health, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DU, UK

4. Caribbean Center for Child Neurodevelopment, Windward Islands Research and Education Foundation, St. George P.O. Box 7, Grenada

5. Department of Pediatrics, Infectious Disease Division, Stanford University School of Medicine, Stanford, CA 94304, USA

6. Department of Physiology, Neuroscience, and Behavioral Science, School of Medicine, St. George’s University, St. George P.O. Box 7, Grenada

7. Department of Psychiatry and Psychology, Mayo Clinic, Jacksonville, FL 32224, USA

Abstract

Maternal infection with Zika virus (ZIKV) is associated with a distinct pattern of birth defects, known as congenital Zika syndrome (CZS). In ZIKV-exposed children without CZS, it is often unclear whether they were protected from in utero infection and neurotropism. Early neurodevelopmental assessment is essential for detecting neurodevelopmental delays (NDDs) and prioritizing at-risk children for early intervention. We compared neurodevelopmental outcomes between ZIKV-exposed and unexposed children at 1, 3 and 4 years to assess exposure-associated NDD risk. A total of 384 mother–child dyads were enrolled during a period of active ZIKV transmission (2016–2017) in Grenada, West Indies. Exposure status was based on laboratory assessment of prenatal and postnatal maternal serum. Neurodevelopment was assessed using the Oxford Neurodevelopment Assessment, the NEPSY® Second Edition and Cardiff Vision Tests, at 12 (n = 66), 36 (n = 58) and 48 (n = 59) months, respectively. There were no differences in NDD rates or vision scores between ZIKV-exposed and unexposed children. Rates of microcephaly at birth (0.88% vs. 0.83%, p = 0.81), and childhood stunting and wasting did not differ between groups. Our results show that Grenadian ZIKV-exposed children, the majority of whom were without microcephaly, had similar neurodevelopmental outcomes to unexposed controls up to at least an age of 4 years.

Funder

St. George’s University

US Agency for International Development

National Institutes of Health

Stanford Maternal Child Health Research Institute New Ideas Award

Medical Research Council

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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