# Association between depression during pregnancy and preterm birth: Results from population cohorts and mouse experimental models

**Authors:** Siguo Chen, Guanghong Yan, Xinzi Xie, Qihan Wang, Jie Zhong, Qian Wang, Jinman Zhang, Hongying Li, Dingyun You, Mengstu Melkamu Asaye, Samson Nivins, Samson Nivins, Samson Nivins, Samson Nivins

PMC · DOI: 10.1371/journal.pone.0341449 · 2026-01-29

## TL;DR

Pregnant women with depression are more likely to give birth early, and this was confirmed in both human and mouse studies.

## Contribution

This study provides new evidence from a Chinese cohort and a mouse model linking prenatal depression to preterm birth.

## Key findings

- Women with depressive symptoms had a 2.19 times higher risk of preterm birth.
- Mouse models exposed to stress showed a 40% preterm birth rate, compared to none in controls.
- A dose-response relationship was observed between depression severity and preterm birth risk.

## Abstract

Depression is a prevalent psychological challenge during pregnancy, with established links to adverse outcomes like preterm birth (PTB) globally. However, epidemiological data from China’s multiethnic regions are scarce, and experimental evidence supporting a causal relationship remains limited. This study aimed to investigate the association between prenatal depressive symptoms and the risk of PTB in a cohort from Yunnan, China, and to provide supportive evidence using a mouse model of depression.

We recruited 1,466 women during their first-trimester routine visits at Qujing Hospital. Depressive symptoms were assessed using the Chinese version of the Edinburgh Postnatal Depression Scale (EPDS), a screening tool, with a score ≥12 indicating elevated symptoms suggestive of depression. PTB was defined as delivery before 37 gestational weeks, confirmed by ultrasound. In parallel, a mouse model of depression was established using Chronic Unpredictable Mild Stress (CUMS) for 6 weeks prior to mating. PTB in mice was defined as delivery before 19 days of gestation.

In the cohort study, the incidence of PTB was significantly higher in women with prenatal depressive symptoms compared to those without (8.43% vs. 3.83%, P < 0.001). The association remained significant after adjusting for sociodemographic and clinical confounders, with an adjusted risk ratio (aRR) of 2.19 (95% CI: 1.32–3.63). This association showed a significant dose-response pattern (P for trend = 0.03), with the risk being highest for women with moderate depressive symptoms (aRR = 2.44, 95% CI: 1.30–4.58). In the animal experiments, PTB did not occur in the control mice, whereas 40% of the mice exposed to CUMS (depression model group) delivered prematurely.

This study demonstrates a significant association between prenatal depressive symptoms and an increased risk of preterm birth in a Chinese multiethnic cohort. Experimental findings from a mouse model further suggest a potential contributory role of depression to PTB. These results underscore the importance of screening for and addressing maternal mental health during pregnancy. Future research should focus on underlying mechanisms and intervention strategies to mitigate this risk.

## Linked entities

- **Diseases:** depression (MONDO:0002050)
- **Species:** Homo sapiens (taxon 9606), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** AGXT (alanine--glyoxylate aminotransferase) [NCBI Gene 189] {aka AGT, AGT1, AGXT1, PH1, SPAT, SPT}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, PTBP1 (polypyrimidine tract binding protein 1) [NCBI Gene 5725] {aka HNRNP-I, HNRNPI, HNRPI, PTB, PTB-1, PTB-T}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** stillbirth (MESH:D050497), infection (MESH:D007239), HPA axis dysregulation (MESH:D007029), mental disorder (MESH:D001523), preeclampsia (MESH:D011225), neurodevelopmental problems (MESH:D019973), analgesia (MESH:D000699), fetal arrest (MESH:D005315), COVID (MESH:D000086382), Depression (MESH:D003866), labor (MESH:D048949), gestational diabetes (MESH:D016640), gestational hypertension (MESH:D046110), PTB (MESH:D047928), birth defects (MESH:D000014), miscarriage (MESH:D000022), trauma (MESH:D014947), anhedonia (MESH:D059445), premature labor (MESH:D007752), Non-psychotic mental disorders (MESH:D019965), dislocation (MESH:D004204), pregnancy depression (MESH:D011254), congenital heart disease (MESH:D006330), mental distress (MESH:D012128), Affect Disord (MESH:D019964), gain (MESH:D015430), inflammation (MESH:D007249), CUMS (MESH:D000079225), anxiety (MESH:D001007)
- **Chemicals:** sugar (MESH:D000073893), cortisol (MESH:D006854), PONE-D-24-60622 (-), sucrose (MESH:D013395), water (MESH:D014867), isoflurane (MESH:D007530)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12854446/full.md

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Source: https://tomesphere.com/paper/PMC12854446