Maternal exposure to childhood maltreatment and adverse birth outcomes.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
27 06 2023
Historique:
received: 06 01 2023
accepted: 10 06 2023
medline: 29 6 2023
pubmed: 28 6 2023
entrez: 27 6 2023
Statut: epublish

Résumé

Exposure to traumatic events during pregnancy may influence pregnancy and birth outcomes. Growing evidence suggests that exposure to traumatic events well before pregnancy, such as childhood maltreatment (CM), also may influence the course of pregnancy and risk of adverse birth outcomes. We aimed to estimate associations between maternal CM exposure and small-for-gestational-age birth (SGA) and preterm birth (PTB) in a diverse US sample, and to examine whether common CM-associated health and behavioral sequelae either moderate or mediate these associations. The Measurement of Maternal Stress (MOMS) Study was a prospective cohort study that enrolled 744 healthy English-speaking participants ≥ 18 years with a singleton pregnancy, who were < 21 weeks at enrollment, between 2013 and 2015. CM was measured via the Childhood Trauma Questionnaire (CTQ) and participants above the moderate/severe cut-off for any of the five childhood abuse and neglect scales were assigned to the CM-exposed group. Common CM-associated health (obesity, depressive symptoms, hypertensive disorders) and behavioral (substance use) sequelae were obtained from standardized questionnaires and medical records. The main outcomes included PTB (gestational age < 37 weeks at birth) and SGA (birthweight < 10%ile for gestational age) abstracted from the medical record. Multivariable logisitic regression was used to test associations between CM, sequeale, and birth outcomes, and both moderation and mediation by CM-related sequelae were tested. Data were available for 657/744 participants. Any CM exposure was reported by 32% of participants. Risk for SGA birth was 61% higher among those in the CM group compared to the non-CM group (14.1% vs. 7.6%), and each subsequent form of CM that an individual was exposed to corresponded with a 27% increased risk for SGA (aOR 1.27, 95% CI 1.05, 1.53). There was no significant association between CM and PTB (9.3% vs. 13.0%, aOR 1.07, 95% CI 0.58, 1.97). Of these sequelae only hypertensive disorders were associated with both CM and SGA and hypertensive disorders of pregnancy did not mediate the association between CM and SGA. Our findings indicate that maternal CM exposure is associated with increased risk for SGA birth and highlight the importance of investigating the mechanisms whereby childhood adversity sets the trajectory for long-term and intergenerational health issues.

Identifiants

pubmed: 37369688
doi: 10.1038/s41598-023-36831-9
pii: 10.1038/s41598-023-36831-9
pmc: PMC10300045
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

10380

Subventions

Organisme : NIH HHS
ID : HHSN275201200007I--HHSN27500005
Pays : United States
Organisme : NIH HHS
ID : R01 MH-105538
Pays : United States
Organisme : European Research Council
ID : ERC-Stg 639766
Pays : International
Organisme : NIH HHS
ID : UH3 OD-023349
Pays : United States
Organisme : NIH HHS
ID : UH3 OD023349
Pays : United States
Organisme : NICHD NIH HHS
ID : HHSN275201200007C
Pays : United States

Informations de copyright

© 2023. The Author(s).

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Auteurs

Lauren S Keenan-Devlin (LS)

, Evanston, IL, USA.
Department of Obstetrics and Gynecology, NorthShore University HealthSystem, Evanston, USA.
University of Chicago Pritzker School of Medicine, Chicago, USA.

Ann E B Borders (AEB)

, Evanston, IL, USA.
Department of Obstetrics and Gynecology, NorthShore University HealthSystem, Evanston, USA.
University of Chicago Pritzker School of Medicine, Chicago, USA.
Institute for Public Health and Medicine, Northwestern University Center for Healthcare Studies, Chicago, USA.

Alexa Freedman (A)

, Evanston, IL, USA.
Department of Obstetrics and Gynecology, NorthShore University HealthSystem, Evanston, USA.
Department of Psychology, Northwestern University, Evanston, USA.
Institute for Policy Research, Northwestern University, Evanston, USA.

Gregory E Miller (GE)

, Evanston, IL, USA.
Department of Psychology, Northwestern University, Evanston, USA.
Institute for Policy Research, Northwestern University, Evanston, USA.

William Grobman (W)

Institute for Public Health and Medicine, Northwestern University Center for Healthcare Studies, Chicago, USA.
, Chicago, IL, USA.
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Northwestern University Feinberg School of Medicine, Evanston, USA.

Sonja Entringer (S)

, Berlin, Germany.
Department of Medical Psychology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Augustenburger Platz 1, 13353, Berlin, Germany.
Development, Health and Disease Research Program, UC University of California Irvine, California, USA.

Hyagriv Simhan (H)

, Pittsburgh, PA, USA.
Division of Maternal-Fetal Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, USA.

Pathik Wadhwa (P)

Development, Health and Disease Research Program, UC University of California Irvine, California, USA.
, Irvine, CA, USA.

Claudia Buss (C)

, Berlin, Germany. claudia.buss@charite.de.
Department of Medical Psychology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Augustenburger Platz 1, 13353, Berlin, Germany. claudia.buss@charite.de.
Development, Health and Disease Research Program, UC University of California Irvine, California, USA. claudia.buss@charite.de.
Department of Pediatrics, Development, Health and Disease Research Program, University of California Irvine, 1001 Health Sciences Road, Irvine, CA, 92697-3950, USA. claudia.buss@charite.de.

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