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Joint effects of recent stressful life events and adverse childhood experiences on perinatal comorbid anxiety and depression
BACKGROUND: Stressful life events (SLEs) and adverse childhood experiences (ACEs) have been reported to be associated with perinatal depression (PND) or perinatal anxiety (PNA) alone; however, in most cases, majority of PND and PNA coexist and could lead to more serious health consequences. The inde...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847044/ https://www.ncbi.nlm.nih.gov/pubmed/36653742 http://dx.doi.org/10.1186/s12884-023-05375-1 |
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author | Hou, Yanyan Shang, Mengqing Yu, Xiayan Gu, Yue Li, Haiyan Lu, Mengjuan Jiang, Minmin Zhen, Hualong Zhu, Beibei Tao, Fangbiao |
author_facet | Hou, Yanyan Shang, Mengqing Yu, Xiayan Gu, Yue Li, Haiyan Lu, Mengjuan Jiang, Minmin Zhen, Hualong Zhu, Beibei Tao, Fangbiao |
author_sort | Hou, Yanyan |
collection | PubMed |
description | BACKGROUND: Stressful life events (SLEs) and adverse childhood experiences (ACEs) have been reported to be associated with perinatal depression (PND) or perinatal anxiety (PNA) alone; however, in most cases, majority of PND and PNA coexist and could lead to more serious health consequences. The independent effect of recent SLEs and their joint effects with ACEs on perinatal comorbid anxiety and depression (CAD) remain inadequately explored. METHODS: Based on a longitudinal study, 1082 participants receiving prenatal care in Ma’anshan, China were included. Women were recruited in the first trimester (T1: ≤14(+ 6) weeks) and followed up at 15 ~ 27 weeks (T2), 28 ~ 40 weeks (T3), and postpartum (T4). Depression and anxiety status were assessed at all time points, while recent SLEs and ACEs were measured at T1. Logistic regression was conducted to examine the associations of SLEs with the risks of CAD at different time points, as well as their joint effects with ACEs on CAD. RESULTS: Approximately 38.5% of women experienced at least one SLE, which was significantly associated with higher risks of CAD at all time points (p < 0.05). As the number of SLEs increased, the risk of CAD increased (p for trend < 0.05). Specific types of SLEs were associated with CAD in different periods, while only interpersonal events were consistently associated with risks of CAD throughout the whole perinatal period. The joint effects of SLEs with ACEs on CAD were identified throughout the perinatal period, with the highest observed in the first trimester (aOR = 7.47, 95% CI: 3.73–14.95; p for trend < 0.001). CONCLUSION: Our study demonstrated independent associations of recent SLEs and their joint effects with ACEs with risks of perinatal CAD. SLEs combined with ACEs should be recognized as a major risk factor for perinatal CAD and managed at the earliest time to prevent and control CAD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-023-05375-1. |
format | Online Article Text |
id | pubmed-9847044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98470442023-01-19 Joint effects of recent stressful life events and adverse childhood experiences on perinatal comorbid anxiety and depression Hou, Yanyan Shang, Mengqing Yu, Xiayan Gu, Yue Li, Haiyan Lu, Mengjuan Jiang, Minmin Zhen, Hualong Zhu, Beibei Tao, Fangbiao BMC Pregnancy Childbirth Research BACKGROUND: Stressful life events (SLEs) and adverse childhood experiences (ACEs) have been reported to be associated with perinatal depression (PND) or perinatal anxiety (PNA) alone; however, in most cases, majority of PND and PNA coexist and could lead to more serious health consequences. The independent effect of recent SLEs and their joint effects with ACEs on perinatal comorbid anxiety and depression (CAD) remain inadequately explored. METHODS: Based on a longitudinal study, 1082 participants receiving prenatal care in Ma’anshan, China were included. Women were recruited in the first trimester (T1: ≤14(+ 6) weeks) and followed up at 15 ~ 27 weeks (T2), 28 ~ 40 weeks (T3), and postpartum (T4). Depression and anxiety status were assessed at all time points, while recent SLEs and ACEs were measured at T1. Logistic regression was conducted to examine the associations of SLEs with the risks of CAD at different time points, as well as their joint effects with ACEs on CAD. RESULTS: Approximately 38.5% of women experienced at least one SLE, which was significantly associated with higher risks of CAD at all time points (p < 0.05). As the number of SLEs increased, the risk of CAD increased (p for trend < 0.05). Specific types of SLEs were associated with CAD in different periods, while only interpersonal events were consistently associated with risks of CAD throughout the whole perinatal period. The joint effects of SLEs with ACEs on CAD were identified throughout the perinatal period, with the highest observed in the first trimester (aOR = 7.47, 95% CI: 3.73–14.95; p for trend < 0.001). CONCLUSION: Our study demonstrated independent associations of recent SLEs and their joint effects with ACEs with risks of perinatal CAD. SLEs combined with ACEs should be recognized as a major risk factor for perinatal CAD and managed at the earliest time to prevent and control CAD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-023-05375-1. BioMed Central 2023-01-18 /pmc/articles/PMC9847044/ /pubmed/36653742 http://dx.doi.org/10.1186/s12884-023-05375-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Hou, Yanyan Shang, Mengqing Yu, Xiayan Gu, Yue Li, Haiyan Lu, Mengjuan Jiang, Minmin Zhen, Hualong Zhu, Beibei Tao, Fangbiao Joint effects of recent stressful life events and adverse childhood experiences on perinatal comorbid anxiety and depression |
title | Joint effects of recent stressful life events and adverse childhood experiences on perinatal comorbid anxiety and depression |
title_full | Joint effects of recent stressful life events and adverse childhood experiences on perinatal comorbid anxiety and depression |
title_fullStr | Joint effects of recent stressful life events and adverse childhood experiences on perinatal comorbid anxiety and depression |
title_full_unstemmed | Joint effects of recent stressful life events and adverse childhood experiences on perinatal comorbid anxiety and depression |
title_short | Joint effects of recent stressful life events and adverse childhood experiences on perinatal comorbid anxiety and depression |
title_sort | joint effects of recent stressful life events and adverse childhood experiences on perinatal comorbid anxiety and depression |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847044/ https://www.ncbi.nlm.nih.gov/pubmed/36653742 http://dx.doi.org/10.1186/s12884-023-05375-1 |
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