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Published on: June 13, 2021
SSRIs in pregnancy and lactation: emphasis on neurodevelopmental outcome
1Department of Mental Health, ASL Salerno 1, Salerno, Italy. salvatore_gentile@aliceposta.it
Insights
Maternal use of selective serotonin reuptake inhibitors (SSRIs) during pregnancy and breastfeeding shows mixed results for infant neurodevelopment. While most studies indicate no adverse effects, some suggest subtle motor development issues, necessitating further research.
Area of Science:
- Neuroscience
- Developmental Psychology
- Pharmacology
Background:
- Selective serotonin reuptake inhibitors (SSRIs) are commonly prescribed during pregnancy and breastfeeding.
- Concerns exist regarding potential long-term neurocognitive effects on infants exposed to SSRIs in utero or via breast milk.
Purpose of the Study:
- To review and synthesize existing literature on the long-term neurocognitive development of children exposed to SSRIs during pregnancy and/or breastfeeding.
- To assess the evidence for adverse neurodevelopmental outcomes following prenatal and/or postnatal SSRI exposure.
Main Methods:
- Systematic review of 13 studies (387 children total) examining neurocognitive development after maternal SSRI exposure.
- Analysis of studies reporting no neurodevelopmental impairment versus those suggesting possible adverse effects.
Main Results:
- Eleven studies (306 children) found no neurodevelopmental impairment in infants exposed to SSRIs.
- Two studies (81 children) indicated potential subtle adverse effects on motor development and control.
- The majority of evidence suggests a lack of adverse neurocognitive events, though methodological limitations exist across all studies.
Conclusions:
- Current data on SSRI exposure and infant neurodevelopment are inconclusive due to study limitations and small sample sizes.
- While most infants show no adverse effects, individual variability in drug metabolism means potential risks cannot be entirely excluded.
- Larger, well-designed, prospective studies with robust neurophysiological measures are needed to definitively establish the safety of maternal SSRI use.
Abstract:
The aim of this review was to assess existing information about the long-term neurocognitive development of children whose mothers took SSRIs during pregnancy and/or breastfeeding. The available literature consists of 11 studies (examining a total of 306 children) that demonstrate no impairment of infant neurodevelopment following prenatal and/or postnatal exposure to SSRIs, and two studies (examining 81 children) that suggest possible unwanted effects of fetal SSRI exposure. These unwanted effects included subtle effects on motor development and motor control. Thus, the available data are not unanimous in excluding possible long-term detrimental neurodevelopmental sequelae of intrauterine exposure to SSRIs. However, it is clear that the research suggesting a lack of adverse events on infants' neurocognitive development is much more numerous and methodologically better conducted than the studies showing possible unwanted effects. Nevertheless, all reviewed studies had procedural inadequacies, and the screening instruments used have limitations, especially in the evaluation of infants. Furthermore, it is not advisable to extend the generalisations emerging from the findings of a few trials to every infant. Some infants may experience difficulties in metabolising the drugs and/or their metabolites, so the benign outcome described for most infants may not occur. Thus, the findings emerging from the reports are inconclusive and are not able to fully clarify the repercussions of maternal SSRI treatment on infants' long-term neurocognitive development. Further large, simple and well designed, randomised, prospective studies will be required for this purpose. These should also be of adequate length and performed using reproducible neurophysiological parameters in order to firmly establish the safety of these medications.
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