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Published on: June 29, 2013
Fetal growth restriction and the development of major depression
H-M Vasiliadis1, S E Gilman, S L Buka
1Department of Community Health and Sciences, University of Sherbrooke, Sherbrooke, QC, Canada. helen-maria.vasiliadis@usherbrooke.ca
Insights
Fetal growth restriction did not increase the risk of major depression or recurrent depressive episodes in adulthood. This study found no evidence supporting a "fetal programming" effect on depression risk.
Area of Science:
- Perinatal Epidemiology
- Psychiatry
- Developmental Origins of Health and Disease
Background:
- Fetal growth restriction (FGR) is linked to various adverse health outcomes.
- The potential association between FGR and later-life major depressive disorder (MDD) remains unclear.
- Investigating early-life factors for mental health conditions is crucial for public health.
Purpose of the Study:
- To examine the relationship between indicators of fetal growth restriction and the lifetime incidence of major depression.
- To assess if FGR influences the number of recurrent depressive episodes over a lifetime.
- To determine if birth size is a predictor for developing major depression later in life.
Main Methods:
- A cohort of 1101 offspring from the National Collaborative Perinatal Project was analyzed.
- Cox regression models assessed the association between birth size measures (e.g., low birth weight, small for gestational age) and major depression risk.
- Mean depressive episodes were compared across different birth size categories.
Main Results:
- No significant association was found between low birth weight, gestational age, ponderal index, or small for gestational age and the lifetime risk of major depression.
- Fetal growth restriction measures did not correlate with an increased number of recurrent depressive episodes.
- The study found no statistical link between birth size and the development or recurrence of major depression.
Conclusions:
- Fetal growth restriction, indicated by various birth size metrics, is not associated with an increased risk of major depression.
- The findings do not support a 'fetal programming' hypothesis for the development of depression.
- Early life growth appears unrelated to the lifetime risk and recurrence of major depressive disorder.
Objective:
To test the association between fetal growth restriction and the lifetime risk of major depression and the number of recurrent episodes.
Method:
Study subjects (n = 1101) were offspring of participants in the Providence, RI, site of the National Collaborative Perinatal Project. Cox regression was used to investigate the relation between measures of birth size and the lifetime risk of depression and the mean number of depressive episodes was compared across categories of birth size.
Results:
There was no association between low birth weight, gestational age, ponderal index and small for gestational age and the lifetime risk of major depression, or the number of recurrent episodes.
Conclusion:
Fetal growth restriction, as reflected by multiple measures of birth size, is not associated with the risk of a major depression or the subsequent recurrence of depressive episodes. Results of this study do not support a 'fetal programming' effect in depression.
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