Epilepsy surveillance in normocephalic children with and without prenatal Zika virus exposure.
Anticonvulsants
/ therapeutic use
Carbamazepine
/ therapeutic use
Cohort Studies
Electroencephalography
Epilepsy
/ epidemiology
Female
Grenada
/ epidemiology
Humans
Immunoglobulin G
/ blood
Infant
Male
Pregnancy
Pregnancy Complications, Infectious
/ epidemiology
Prospective Studies
Zika Virus
/ isolation & purification
Zika Virus Infection
/ complications
Journal
PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488
Informations de publication
Date de publication:
11 2020
11 2020
Historique:
received:
28
04
2020
accepted:
12
10
2020
revised:
10
12
2020
pubmed:
1
12
2020
medline:
23
1
2021
entrez:
30
11
2020
Statut:
epublish
Résumé
Children with Congenital Zika Syndrome and microcephaly are at high risk for epilepsy; however, the risk is unclear in normocephalic children with prenatal Zika virus (ZIKV) exposure [Exposed Children (EC)]. In this prospective cohort study, we performed epilepsy screening in normocephalic EC alongside a parallel group of normocephalic unexposed children [Unexposed Children (UC)]. We compared the incidence rate of epilepsy among EC and UC at one year of life to global incidence rates. Pregnant women were recruited from public health centers during the ZIKV outbreak in Grenada, West Indies and assessed for prior ZIKV infection using a plasmonic-gold platform that measures IgG antibodies in serum. Normocephalic children born to mothers with positive ZIKV results during pregnancy were classified as EC and those born to mothers with negative ZIKV results during and after pregnancy were classified as UC. Epilepsy screening procedures included a pediatric epilepsy screening questionnaire and video electroencephalography (vEEG). vEEG was collected using a multi-channel microEEG® system for a minimum of 20 minutes along with video recording of participant behavior time-locked to the EEG. vEEGs were interpreted independently by two pediatric epileptologists, who were blinded to ZIKV status, via telemedicine platform. Positive screening cases were referred to a local pediatrician for an epilepsy diagnostic evaluation. Epilepsy screens were positive in 2/71 EC (IR: 0.028; 95% CI: 0.003-0.098) and 0/71 UC. In both epilepsy-positive cases, questionnaire responses and interictal vEEGs were consistent with focal, rather than generalized, seizures. Both children met criteria for a clinical diagnosis of epilepsy and good seizure control was achieved with carbamazepine. Our results indicate that epilepsy rates are modestly elevated in EC. Given our small sample size, results should be considered preliminary. They support the use of epilepsy screening procedures in larger epidemiological studies of children with congenital ZIKV exposure, even in the absence of microcephaly, and provide guidance for conducting epilepsy surveillance in resource limited settings.
Identifiants
pubmed: 33253174
doi: 10.1371/journal.pntd.0008874
pii: PNTD-D-20-00713
pmc: PMC7728266
doi:
Substances chimiques
Anticonvulsants
0
Immunoglobulin G
0
Carbamazepine
33CM23913M
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0008874Subventions
Organisme : NIBIB NIH HHS
ID : R01 EB019805
Pays : United States
Organisme : NICHD NIH HHS
ID : R21 HD093551
Pays : United States
Déclaration de conflit d'intérêts
I have read the journal's policy and the authors of this manuscript have the following competing interests: Dr. Samah G. Abdel Baki reports support from Bio-Signal Group Corporation and other grants outside the submitted work. In addition, Dr. Baki has a patent 61/554,743 pending and a U.S. patent 13/284,886. None of the other authors have competing interests to disclose.
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