Maternal prenatal stress and placental gene expression of NR3C1 and HSD11B2; the effects of maternal ethnicity
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Accepted version
Author(s)
Capron, L
Ramchandani, P
Glover, V
Type
Journal Article
Abstract
Background
Prenatal stress is associated with altered fetal and infant development. Previous studies have suggested that these effects may be mediated in part via altered functioning of placental enzymes and receptors involved in the HPA-axis, including the glucocorticoid receptor (NR3C1) and HSD11B2, the enzyme which metabolises cortisol. However, previous studies have not examined the potential ethnicity effects on these associations. This study aimed to characterise the association between maternal prenatal stress and placental genes expression and subsequently, any potential effect of maternal ethnicity.
Method
Pregnant women(n = 83) were recruited prior to elective caesarean section and assessed for trait anxiety, depression and life events. Placentas were collected and placental gene expression of NR3C1 and HSD11B2 were analysed. We examined associations between maternal prenatal stress and placental gene expression, and the tested for a possible moderating effect of maternal ethnicity(59.0% Caucasian;41.0% non-Caucasian:12.0% South Asian;6.0% African/African-American;14.4% Other;8.4% Mixed).
Results
Analyses demonstrated a trend in the association between both maternal trait anxiety and depression symptoms with placental gene expression of NR3C1(adj.β = .220,p = .067;adj.β = .212,p = .064 respectively). We found a significant interaction with maternal ethnicity(β = .249;p = .033). In Caucasian women only prenatal trait anxiety and depressive symptoms were associated with an increase in placental NR3C1 expression(adj.β = .389,p = .010;adj.β = .294;p = .047 respectively). Prenatal life events were associated with a down regulation of HSD11B2(adj.β = .381;p = .008), but only in Caucasians.
Conclusion
These results support previous findings of an association between maternal prenatal stress and the expression of placental genes associated with the HPA-axis, but only in Caucasians. These ethnic specific findings are novel and require replication in different populations.
Prenatal stress is associated with altered fetal and infant development. Previous studies have suggested that these effects may be mediated in part via altered functioning of placental enzymes and receptors involved in the HPA-axis, including the glucocorticoid receptor (NR3C1) and HSD11B2, the enzyme which metabolises cortisol. However, previous studies have not examined the potential ethnicity effects on these associations. This study aimed to characterise the association between maternal prenatal stress and placental genes expression and subsequently, any potential effect of maternal ethnicity.
Method
Pregnant women(n = 83) were recruited prior to elective caesarean section and assessed for trait anxiety, depression and life events. Placentas were collected and placental gene expression of NR3C1 and HSD11B2 were analysed. We examined associations between maternal prenatal stress and placental gene expression, and the tested for a possible moderating effect of maternal ethnicity(59.0% Caucasian;41.0% non-Caucasian:12.0% South Asian;6.0% African/African-American;14.4% Other;8.4% Mixed).
Results
Analyses demonstrated a trend in the association between both maternal trait anxiety and depression symptoms with placental gene expression of NR3C1(adj.β = .220,p = .067;adj.β = .212,p = .064 respectively). We found a significant interaction with maternal ethnicity(β = .249;p = .033). In Caucasian women only prenatal trait anxiety and depressive symptoms were associated with an increase in placental NR3C1 expression(adj.β = .389,p = .010;adj.β = .294;p = .047 respectively). Prenatal life events were associated with a down regulation of HSD11B2(adj.β = .381;p = .008), but only in Caucasians.
Conclusion
These results support previous findings of an association between maternal prenatal stress and the expression of placental genes associated with the HPA-axis, but only in Caucasians. These ethnic specific findings are novel and require replication in different populations.
Date Issued
2017-10-26
Date Acceptance
2017-10-25
Citation
Psychoneuroendocrinology, 2017, 87, pp.166-172
ISSN
0306-4530
Publisher
Elsevier
Start Page
166
End Page
172
Journal / Book Title
Psychoneuroendocrinology
Volume
87
Copyright Statement
© 2017, Elsevier. Licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/
Sponsor
Imperial College Healthcare NHS Trust- BRC Funding
Grant Number
RDA03
Subjects
Anxiety
Depression
Placenta and ethnicity
Prenatal
11 Medical And Health Sciences
17 Psychology And Cognitive Sciences
Psychiatry
Publication Status
Published online