Two-Year-Old Cognitive Outcomes in Children of Pregnant Women With Epilepsy in the Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs Study

The neurodevelopmental risks of fetal exposure are uncertain for many antiseizure medications (ASMs). To compare children at 2 years of age who were born to women with epilepsy (WWE) vs healthy women and assess the association of maximum ASM exposure in the third trimester and subsequent cognitive a...

Full description

Saved in:
Bibliographic Details
Published inArchives of neurology (Chicago) Vol. 78; no. 8; p. 927
Main Authors Meador, Kimford J, Cohen, Morris J, Loring, David W, May, Ryan C, Brown, Carrie, Robalino, Chelsea P, Matthews, Abigail G, Kalayjian, Laura A, Gerard, Elizabeth E, Gedzelman, Evan R, Penovich, Patricia E, Cavitt, Jennifer, Hwang, Sean, Sam, Maria, Pack, Alison M, French, Jacqueline, Tsai, Jeffrey J, Pennell, Page B
Format Journal Article
LanguageEnglish
Published United States American Medical Association 01.08.2021
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The neurodevelopmental risks of fetal exposure are uncertain for many antiseizure medications (ASMs). To compare children at 2 years of age who were born to women with epilepsy (WWE) vs healthy women and assess the association of maximum ASM exposure in the third trimester and subsequent cognitive abilities among children of WWE. The Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs (MONEAD) study is a prospective, observational, multicenter investigation of pregnancy outcomes that enrolled women from December 19, 2012, to January 13, 2016, at 20 US epilepsy centers. Children are followed up from birth to 6 years of age, with assessment at 2 years of age for this study. Of 1123 pregnant women assessed, 456 were enrolled; 426 did not meet criteria, and 241 chose not to participate. Data were analyzed from February 20 to December 4, 2020. Language domain score according to the Bayley Scales of Infant and Toddler Development, Third Edition (BSID-III), which incorporates 5 domain scores (language, motor, cognitive, social-emotional, and general adaptive), and association between BSID-III language domain and ASM blood levels in the third trimester in children of WWE. Analyses were adjusted for multiple potential confounding factors, and measures of ASM exposure were assessed. The BSID-III assessments were analyzed in 292 children of WWE (median age, 2.1 [range, 1.9-2.5] years; 155 female [53.1%] and 137 male [46.9%]) and 90 children of healthy women (median age, 2.1 [range, 2.0-2.4] years; 43 female [47.8%] and 47 male [52.2%]). No differences were found between groups on the primary outcome of language domain (-0.5; 95% CI, -4.1 to 3.2). None of the other 4 BSID-III domains differed between children of WWE vs healthy women. Most WWE were taking lamotrigine and/or levetiracetam. Exposure to ASMs in children of WWE showed no association with the language domain. However, secondary analyses revealed that higher maximum observed ASM levels in the third trimester were associated with lower BSID-III scores for the motor domain (-5.6; 95% CI, -10.7 to -0.5), and higher maximum ASM doses in the third trimester were associated with lower scores in the general adaptive domain (-1.4; 95% CI, -2.8 to -0.05). Outcomes of children at 2 years of age did not differ between children of WWE taking ASMs and children of healthy women. ClinicalTrials.gov Identifier: NCT01730170.
ISSN:2168-6149
2168-6157
DOI:10.1001/jamaneurol.2021.1583