A Scoping Review of Human Teratogens and Their Impact on the Developing Brain: A Contribution From the ConcePTION Project

ABSTRACT Certain medications, when used during pregnancy, are known to impact human prenatal development. Historically, little attention has been given to the impact of in utero exposure on the developing brain, despite the significance of known teratogen‐induced neurodevelopmental difficulties. Thi...

Full description

Saved in:
Bibliographic Details
Published in:Birth defects research Vol. 117; no. 9; pp. e2497 - n/a
Main Authors: Bluett‐Duncan, M., Adams, J., Berkovitch, M., Berlin, M., Cahoon, A., Clayton‐Smith, J., Jackson, C., Khanom, S., Mølgaard‐Nielsen, D., Richardson, J. L., Simms, V., Stellfeld, M., Winterfeld, U., Yates, L. M., Bromley, R. L.
Format: Journal Article
Language:English
Published: Hoboken, USA John Wiley & Sons, Inc 01.09.2025
Wiley Subscription Services, Inc
Subjects:
ISSN:2472-1727, 2472-1727
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:ABSTRACT Certain medications, when used during pregnancy, are known to impact human prenatal development. Historically, little attention has been given to the impact of in utero exposure on the developing brain, despite the significance of known teratogen‐induced neurodevelopmental difficulties. This scoping review systematically identified and extracted neurodevelopmental outcome data for medications with established physical teratogenic effects and synthesized the key study characteristics. Medications with evidence of physical teratogenicity (n = 24) were defined by a panel of experts. Eligible studies reporting any neurodevelopmental outcomes following pregnancy exposure to the defined list of human structural teratogens were identified through electronic searches of MEDLINE and EMBASE. We identified 207 studies (254 publications) for inclusion, comprising 81 empirical cohorts and 126 case series. Concerningly, only 13 of 24 (54%) confirmed structural teratogens have been subject to any empirical investigation of neurodevelopmental outcomes. The mean time between authorization of known structural teratogens and the first empirical study investigating neurodevelopmental outcomes using a comparison group and formal data analysis is 33 years (Range: 11–64 years). When neurodevelopmental outcomes are investigated for medication exposures with physical teratogenic signatures, there are high levels of neurodevelopmental alterations (77%). These findings do not speak to a pharmacovigilance system that is functioning efficiently to identify and ameliorate neurodevelopmental risk, even for the medications with identified structural teratogenic risk. Given the high proportion of known physical teratogens exhibiting additional altered neurodevelopmental outcomes and the substantial lifetime burden of such alterations, to the individual and society, the timelines remain too long.
Bibliography:Funding
This work was supported by Innovative Medicines Initiative.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-4
content type line 23
ObjectType-Undefined-3
ISSN:2472-1727
2472-1727
DOI:10.1002/bdr2.2497