Evidence map›Paper›PMID 41462378›Full record

ArticleBMC psychology2025

The role of perinatal perceived stress in the setting of adverse childhood experience and perinatal anxiety and depressive symptoms.

Folasade Ilori, Nickie N Andescavage, Katherine L Wisner, Julius S Ngwa, Rathinaswamy B Govindan, Catherine Limperopoulos

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Article in BMC psychology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Folasade IloriDeveloping Brain Institute, Children's National Hospital, 111 Michigan Ave NW, Washington, DC, 20010, USA.
Nickie N AndescavageDeveloping Brain Institute, Children's National Hospital, 111 Michigan Ave NW, Washington, DC, 20010, USA.
Katherine L WisnerDeveloping Brain Institute, Children's National Hospital, 111 Michigan Ave NW, Washington, DC, 20010, USA.
Julius S NgwaDeveloping Brain Institute, Children's National Hospital, 111 Michigan Ave NW, Washington, DC, 20010, USA.
Rathinaswamy B GovindanDeveloping Brain Institute, Children's National Hospital, 111 Michigan Ave NW, Washington, DC, 20010, USA.
Catherine LimperopoulosDeveloping Brain Institute, Children's National Hospital, 111 Michigan Ave NW, Washington, DC, 20010, USA. CLimpero@childrensnational.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdverse childhood experiences (ACE) are highly prevalent, with long-lasting effects on physical and mental health that vary among individuals across their lifespan. Notably, ACE is associated with depression and anxiety disorders, which are major public health concerns. However, the factors involved in the detrimental effects of ACE on women in the perinatal period, a time of heightened vulnerability to physical and mental health outcomes for both mothers and their offspring, require further investigation.

methodsTo investigate the role of perceived stress in the association between ACE and maternal depressive and anxiety symptoms across the perinatal period, we included 138 pregnant women recruited for a prospective longitudinal study that examined the effects of increased maternal prenatal stress on pregnancy during the COVID-19 pandemic. Participants self-reported adverse childhood experiences and serial measures of perceived stress, anxiety, and depressive symptoms. Linear mixed-effects (LME) models were employed to assess the association between ACE, perceived stress, anxiety, and depressive symptoms and to determine an interaction effect between ACE and perceived stress on state anxiety, trait anxiety, and depressive symptoms.

resultsOn average, participants were 34 years of age and at 26 weeks of gestation (gestational age; GA). We found a significant interaction between ACE and perceived stress on trait anxiety (β = 0.06, SE = 0.01, p < .001) and depressive symptoms (β = 0.07, SE = 0.01, p < .001) in the perinatal period. Perceived stress moderated the association between ACE and trait anxiety symptoms in the third trimester (β = 0.07, SE = 0.02, p < .001). The association between ACE and depressive symptoms was moderated by perceived stress in the first trimester (β = 0.23, SE = 0.09, p < .05), second trimester (β = 0.09, SE = 0.03, p < .05), and third trimester (β = 0.04, SE = 0.02, p < .05).

conclusionThese findings underscore the importance of assessing ACE as a risk factor when evaluating maternal mental health to identify individuals susceptible to depressive and anxiety disorders in the perinatal period. Moreover, multiple mental health screenings in the perinatal period reduce the risk of missed opportunities for intervention and preventative actions.

Indexed as

Adverse Childhood ExperiencesAnxietyCOVID-19DepressionPregnancy ComplicationsStress, PsychologicalAdultFemaleHumansLongitudinal StudiesPregnancyProspective StudiesAdverse childhood experienceMental healthPerinatal period

Identifiers

PMID41462378
PMCPMC12751169

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.