A Birth Cohort Follow-Up Study on Congenital Zika Virus Infection in Vietnam

Author:

Toizumi Michiko1ORCID,Vu Cuong Nguyen2,Huynh Hai Thi2,Uematsu Masafumi3ORCID,Tran Vy Thao4,Vo Hien Minh4,Nguyen Hien Anh Thi5,Ngwe Tun Mya Myat67ORCID,Bui Minh Xuan2,Dang Duc Anh5,Moriuchi Hiroyuki8ORCID,Yoshida Lay-Myint1ORCID

Affiliation:

1. Department of Pediatric Infectious Diseases, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852-8523, Japan

2. Khanh Hoa Health Service, Nha Trang 650000, Vietnam

3. Department of Ophthalmology, Nagasaki University Hospital, Nagasaki 852-8501, Japan

4. Khanh Hoa General Hospital, Nha Trang 650000, Vietnam

5. National Institute of Hygiene and Epidemiology, Hanoi 100000, Vietnam

6. Department of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852-8523, Japan

7. Center for Vaccines and Therapeutic Antibodies for Emerging Infectious Diseases, Shimane University, Izumo 693-0021, Japan

8. Department of Pediatrics, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan

Abstract

We assessed the development, sensory status, and brain structure of children with congenital Zika virus (ZIKV) infection (CZI) at two years and preschool age. CZI was defined as either ZIKV RNA detection or positive ZIKV IgM and neutralization test in the cord or neonatal blood. Twelve children with CZI born in 2017–2018 in Vietnam, including one with Down syndrome, were assessed at 23–25.5 months of age, using Ages and Stages Questionnaire (ASQ-3), ASQ:Social-Emotional (ASQ:SE-2), Modified Checklist for Autism in Toddlers, automated auditory brainstem response (AABR), and Spot Vision Screener (SVS). They underwent brain CT and MRI. They had detailed ophthalmological examinations, ASQ-3, and ASQ:SE-2 at 51–62 months of age. None had birthweight or head circumference z-score < −3 except for the one with Down syndrome. All tests passed AABR (n = 10). No ophthalmological problems were detected by SVS (n = 10) and detailed examinations (n = 6), except for a girl’s astigmatism. Communication and problem-solving domains in a boy at 24 months, gross-motor area in a boy, and gross-motor and fine-motor areas in another boy at 59–61 months were in the referral zone. Brain CT (n = 8) and MRI (n = 6) revealed no abnormalities in the cerebrum, cerebellum, or brainstem other than cerebellar hypoplasia with Down syndrome. The CZI children were almost age-appropriately developed with no brain or eye abnormalities. Careful and longer follow-up is necessary for children with CZI.

Funder

Maternal and Child Health Association

Japan Agency for Medical Research and Development

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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