# Association of maternal smoking during pregnancy with youth depression and subsequent adult chronic diseases in offspring

**Authors:** Wenming Wei, Bolun Cheng, Xin Qi, Dan He, Shiqiang Cheng, Xuena Yang, Chuyu Pan, Peilin Meng, Jingni Hui, Yifan Gou, Boyue Zhao, Li Liu, Yan Wen, Huan Liu, Yumeng Jia, Feng Zhang

PMC · DOI: 10.1038/s41398-026-03976-w · Translational Psychiatry · 2026-03-26

## TL;DR

Maternal smoking during pregnancy increases the risk of youth depression and chronic diseases in offspring, especially in females and those with high genetic susceptibility.

## Contribution

Identifies genetic variants and gender differences in the impact of maternal smoking on offspring mental and physical health.

## Key findings

- Maternal smoking during pregnancy was linked to a 26% higher risk of youth depression.
- Offspring with high genetic risk scores had a 135% increased risk of youth depression if exposed to maternal smoking.
- Maternal smoking was associated with increased adult risks of asthma, COPD, hypertension, liver disease, and peripheral vascular disease.

## Abstract

This study aimed to elucidate the relationship between maternal smoking during pregnancy (MSDP) and the incidence of youth depression, examine the modifying role of genetic susceptibility, and assess subsequent physical health risks in adulthood. We utilized data from 60,839 participants in the UK Biobank. Cox proportional hazards models were applied to evaluate the impact of MSDP on the onset of youth depression. Genome-wide association studies (GWAS) and gene–environment interaction analyses were conducted to identify genetic variants influencing youth depression and their interactions with MSDP. Polygenic risk scores (PRS) were calculated to assess genetic contributions. Multi-state modeling explored health transitions from MSDP exposure to youth depression and 24 chronic physical diseases in adulthood. The GWAS identified 10 significant SNPs within the ABR gene region (P < 5 × 10−8) associated with youth depression. MSDP was associated with higher risks of youth depression (HR = 1.26, 95% CI: 1.18–1.35), especially among females (HR = 1.34, 95% CI: 1.24–1.45) and participants with high PRS (HR = 2.35, 95% CI: 1.97–2.80). Additionally, MSDP was associated with increased risks of five chronic conditions, including asthma (HR = 1.37, 95% CI: 1.14–1.66), chronic obstructive pulmonary disease (COPD) (HR = 3.53, 95% CI: 2.20–5.65), hypertension(HR = 1.29, 95% CI: 1.12–1.50), liver disease (HR = 1.88, 95% CI: 1.31–2.71), and peripheral vascular disease (HR = 2.33, 95% CI: 1.47–3.71). Notable gender differences in these effects were observed. Overall, MSDP was associated with a greater likelihood of youth depression, especially among females and those with higher genetic susceptibility, and with a higher burden of chronic physical conditions in adulthood. Targeted smoking cessation during pregnancy may therefore yield substantial intergenerational benefits for both mental and physical health.

## Linked entities

- **Genes:** ABR (ABR activator of RhoGEF and GTPase) [NCBI Gene 29]
- **Diseases:** depression (MONDO:0002050), asthma (MONDO:0004979), chronic obstructive pulmonary disease (MONDO:0005002), liver disease (MONDO:0005154), peripheral vascular disease (MONDO:0005294)

## Full-text entities

- **Genes:** BCR (BCR activator of RhoGEF and GTPase) [NCBI Gene 613] {aka ALL, BCR1, CML, D22S11, D22S662, PHL}, LZTS1 (leucine zipper tumor suppressor 1) [NCBI Gene 11178] {aka F37, FEZ1}, ABR (ABR activator of RhoGEF and GTPase) [NCBI Gene 29] {aka MDB}, PDE10A (phosphodiesterase 10A) [NCBI Gene 10846] {aka ADSD2, HSPDE10A, IOLOD, PDE10A19}, CDC42 (cell division cycle 42) [NCBI Gene 998] {aka CDC42Hs, G25K, TKS}, RAC1 (Rac family small GTPase 1) [NCBI Gene 5879] {aka MIG5, MRD48, Rac-1, TC-25, p21-Rac1}, DLG4 (discs large MAGUK scaffold protein 4) [NCBI Gene 1742] {aka MRD62, PSD95, SAP-90, SAP90}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}
- **Diseases:** pulmonary circulation disorders (MESH:D009360), alcohol abuse (MESH:D000437), asthma (MESH:D001249), hypertension (MESH:D006973), depressive behaviors (MESH:D011596), congestive heart failure (MESH:D006333), liver disease (MESH:D008107), neurological disorders (MESH:D009461), cardiovascular diseases (MESH:D002318), behavioral and emotional problems (MESH:D001523), Parkinson's disease (MESH:D010300), internalizing symptoms (MESH:D000082122), blood loss anemia (MESH:D000740), neurotoxic (MESH:D020258), COPD (MESH:D029424), diabetes (MESH:D003920), anxiety (MESH:D001007), valvular disease (MESH:D006349), nicotine dependence (MESH:D014029), MSDP (MESH:D011251), inflammatory (MESH:D007249), seizures (MESH:D012640), cardiac arrhythmia (MESH:D001145), major depression (MESH:D003865), paresis (MESH:D010291), myocardial infarction (MESH:D009203), cerebrovascular disease (MESH:D002561), peptic ulcers (MESH:D010437), circulatory system disorders (MESH:D012769), coagulopathy (MESH:D001778), dementia (MESH:D003704), HIV/AIDS (MESH:D015658), peripheral vascular disease (MESH:D016491), neurodevelopmental disorders (MESH:D002658), epilepsy (MESH:D004827), rheumatic and collagen diseases (MESH:D012216), chronic diseases (MESH:D002908), Depression (MESH:D003866), cancer (MESH:D009369), obesity (MESH:D009765), death (MESH:D003643), paralysis (MESH:D010243), hypothyroidism (MESH:D007037), physical diseases (MESH:D059445), multiple sclerosis (MESH:D009103), renal disease (MESH:D007674)
- **Chemicals:** testosterone (MESH:D013739), Nicotine (MESH:D009538), alcohol (MESH:D000438), cotinine (MESH:D003367), dopamine (MESH:D004298), calcium (MESH:D002118), MSDP (-), glutamate (MESH:D018698)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]
- **Mutations:** rs7844635, rs1484017, rs9459420, rs1542624, rs221753, rs7748041, rs13259502, rs4528676, rs4490643, rs6914589, rs10745943, rs9459419, rs4259393, rs112796437, rs1849204

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC13039871/full.md

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Source: https://tomesphere.com/paper/PMC13039871