Our group of researchers is well-positioned to study the ophthalmic complications of congenital ZIKV. We have been following subjects with ZIKV infection since 2015, during the beginning and peak of infection, including pregnant women and infants born to mothers with PCR proven ZIKV infection. We have a database and specimen bank with over 400 pregnant women with suspected ZIKV infection and ZIKV-exposed infants as they are born. We hypothesize that ophthalmic manifestation of ZIKV reported to date may represent only a part of the full spectrum of disease, because of ascertainment bias. Furthermore, we hypothesize that the extent of ophthalmic findings in ZIKV may correlate to systemic factors such as gestational age at the time of exposure, maternal virus load, microcephaly, and other neurological disorders. We also hypothesize that infants in high-risk settings (born during the time periods and in places of high ZIKV prevalence) may have under? recognized ocular manifestations of ZIKV. We propose to describe the full spectrum of ophthalmic disorders associated with congenital ZIKV infection in infants and its association with the timing of prenatal exposure and development of central nervous system problems. We will also be able to distinguish congenital eye findings of ZIKV from eye findings of other endemic infections (i.e. dengue, chikungunya, toxoplasmosis) in a serologically well-characterized cohort of infants in Brazil. Lastly, in a separate cohort we would like to determine the rate of ophthalmic disease present in high-risk infants born where ZIKV was highly endemic at the time of pregnancy.

Public Health Relevance

ZIKV is an arbovirus causing grave repercussions to unborn infants; including macular atrophy, optic atrophy, and microcephaly. We have an ideal already established cohort of infants to study ophthalmic manifestations of congenital ZIKV. The infants and their mothers have a rich database of biological specimens and clinical data available to correlate with eye findings, and this will greatly enhance knowledge of ZIKV related ocular complications.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21EY028318-01
Application #
9277219
Study Section
Special Emphasis Panel (ZAI1-RRS-M (J1))
Program Officer
Mckie, George Ann
Project Start
2017-03-01
Project End
2019-02-28
Budget Start
2017-03-01
Budget End
2018-02-28
Support Year
1
Fiscal Year
2017
Total Cost
$211,475
Indirect Cost
$55,732
Name
University of California Los Angeles
Department
Pediatrics
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Zin, Andrea A; Tsui, Irena; Rossetto, Julia D et al. (2018) Visual function in infants with antenatal Zika virus exposure. J AAPOS 22:452-456.e1
Adachi, Kristina; Nielsen-Saines, Karin (2018) Zika clinical updates: implications for pediatrics. Curr Opin Pediatr 30:105-116
Zin, Andrea A; Tsui, Irena; Rossetto, Julia et al. (2017) Screening Criteria for Ophthalmic Manifestations of Congenital Zika Virus Infection. JAMA Pediatr 171:847-854
Halai, Umme-Aiman; Nielsen-Saines, Karin; Moreira, Maria Lopes et al. (2017) Maternal Zika Virus Disease Severity, Virus Load, Prior Dengue Antibodies, and Their Relationship to Birth Outcomes. Clin Infect Dis 65:877-883