Early Clinical Infancy Outcomes for Microcephaly and/or Small for Gestational Age Zika-Exposed Infants

Author:

Adachi Kristina1,Romero Tahmineh2,Nielsen-Saines Karin1,Pone Sheila3,Aibe Mitsue3,Barroso de Aguiar Elisa3,Sim Myung2,Brasil Patricia4,Zin Andrea3,Tsui Irena5,Gaw Stephanie L6,Halai Umme-Aiman7,Vasconcelos Zilton3,Pereira Jose Paulo3,Salles Tania Saad3,Barbosa Claudia Neves3,Portari Elyzabeth3,Cherry James D1,Pone Marcos3,Moreira Maria Elisabeth2

Affiliation:

1. Department of Pediatrics, David Geffen School of Medicine, University of California–Los Angeles, California, USA

2. Department of Biostatistics, David Geffen School of Medicine, University of California–Los Angeles, California, USA

3. Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira, Fundação Oswaldo Cruz, Janeiro, Brazil

4. Laboratorio de Doenças Febris Agudas, Instituto de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil

5. Jules Stein Eye Institute, David Geffen School of Medicine, University of California–Los Angeles, California, USA

6. Department of Obstetrics Gynecology, University of California–San Francisco School of Medicine, San Francisco, California, USA

7. Department of Medicine, David Geffen School of Medicine, University of California–Los Angeles, California, USA

Abstract

Abstract Background Zika-exposed infants with microcephaly (proportional or disproportional) and those who are small for gestational age without microcephaly should be closely followed, particularly their growth trajectories. They are at high risk of adverse outcomes in the first year of life. Antenatal Zika virus (ZIKV) exposure may lead to adverse infant outcomes including microcephaly and being small for gestational age (SGA). ZIKV-exposed infants with a diagnosis of microcephaly (proportional [PM] or disproportional [DM]) or SGA at birth were evaluated with anthropometric measurements and health outcomes. Methods Infants had laboratory-confirmed ZIKV exposure in Brazil. PM, DM, or SGA classification was based on head circumference and weight. First-year growth parameters and clinical outcomes were recorded with analyses performed. Results Among the 156 ZIKV-exposed infants, 14 (9.0%) were SGA, 13 (8.3%) PM, 13 (8.3%) DM, and 116 (74.4%) were neither SGA nor had microcephaly (NSNM). High rates of any neurologic, ophthalmologic, and hearing abnormalities were observed for PM (100%), DM (100%), and SGA (42.9%) vs NSNM infants (18.3%; P <.001); odds ratio [OR], 3.4 (95% confidence interval [CI], 1.1–10.7) for SGA vs NSNM. Neuroimaging abnormalities were seen in 100% of PM and DM and in 42.9% of SGA vs NSNM infants 16%; (P <.001); OR 3.9 (95% CI, 1.2–12.8) for SGA vs NSNM. Growth rates by z score, particularly for microcephaly infants, were poor after birth but showed improvement beyond 4 months of life. Conclusions ZIKV-exposed infants with microcephaly (PM and DM) had similarly high rates of adverse outcomes but showed improvement in growth measurements beyond 4 months of life. While SGA infants had fewer adverse outcomes compared with microcephaly infants, notable adverse outcomes were observed in some; their odds of having adverse outcomes were 3 to 4 times greater compared to NSNM infants. Zika-exposed infants with microcephaly, irrespective of being proportional or disproportional, and those who are small for gestational age without microcephaly should be closely followed, particularly their growth trajectories. They are at high risk of adverse outcomes in the first year of life.

Funder

Departamento de Ciência e Tecnologia do Ministério da Saúde do Brasil

Coordenação de Aperfeiçoamento de Pessoal de Nivel Superior

National Institute of Allergy and Infectious Diseases

National Eye Institute

National Institutes of Health (NIH)/National Center for Advancing Translational Science University of California–Los Angeles CTSI

Thrasher Research Fund

Wellcome Trust

European Union’s Horizon 2020

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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