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DNA Methylation Changes Associated With Suicidal Ideation During Pregnancy
Abstract   Peer reviewed

DNA Methylation Changes Associated With Suicidal Ideation During Pregnancy

Marie Gaine, Emma Simpson-Wade, Joelle Ruegg and Alkistis Skalkidou
Biological psychiatry (1969), Vol.99(10 Supplement), pp.S30-S31
05/15/2026
DOI: 10.1016/j.biopsych.2026.03.080

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Abstract

Background One population at high-risk for suicidality are individuals who are pregnant or recently postpartum, and the rate of suicide in this at-risk population is increasing. Compared to suicide deaths during the peripartum period, attempted suicide and suicidal ideation (SI) rates are considerably higher. Pregnancy constitutes one of the most dynamic physiological transitions experienced by women. In addition to the obvious physiological pregnancy adaptations that occur, neurobiological changes are also shown to increase susceptibility to psychiatric disorders. Methods The BASIC Cohort (Uppsala, Sweden) generated DNA methylation data and Edinburgh Postnatal Depression Scale (EPDS) data at 17 weeks gestation (Non-SI participants (NSI)=184; SI=40), 38 weeks gestation (NSI=103; SI=24), and 8 weeks postpartum (NSI=127; SI=31). Results We identified 465, 2,883, and 510 CpGs that were significantly associated with SI at 17 weeks, 38 weeks, and 8 weeks postpartum, respectively (Bonferroni correction p=5.75x10-8). Overlap across the timepoints showed that DNA methylation changes associated with SI are more similar at 38 weeks gestation and 8 weeks postpartum compared to 17 weeks gestation. Notably, when we removed participants on SSRIs, the number of significantly different CpG sites increased, suggesting that individuals on SSRIs may have specific DNA methylation patterns or represent a subtype with different biological mechanisms. Conclusions We provide evidence for DNA methylation differences in association with SI during pregnancy. These patterns are distinct across trimesters suggesting altered DNA methylation, and risk for SI, may have different molecular mechanisms throughout pregnancy. Future work needs to include replication of these findings in independent cohorts and functional studies in mice.

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