Björvang Richelle D, Vrettou Maria, Bujanda Cundin Xabier, Del Prete Eugenio, Rüegg Joëlle, Lager Susanne, di Bernardo Diego, Comasco Erika, Skalkidou Alkistis
Department of Women's and Children's Health, Uppsala University, 751 85, Uppsala, Sweden.
Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Karolinska University Hospital Huddinge K65, SE-14157, Huddinge, Sweden.
Mol Psychiatry. 2025 Jun 5. doi: 10.1038/s41380-025-03068-z.
Peripartum depression can have severe impact on the mother's and the infant's health. Yet, its biological underpinnings are largely unknown. The present study sought to identify transcriptomic signatures of depressive symptoms during pregnancy and postpartum. Blood samples were collected during late pregnancy or early postpartum for mRNA isolation and sequencing, while depressive symptoms were assessed using the Edinburgh Postnatal Depression Scale (EPDS). Based on the timepoint when the samples were collected, differentially expressed genes (DEGs) were identified by (1) comparing mRNA levels between the depression symptom trajectory groups, and (2) correlating with EPDS scores. DEGs for samples collected during late pregnancy, but not postpartum, were associated with depressive symptoms occurring only during pregnancy or persisting postpartum, compared with controls. There were 16 upregulated and 109 downregulated DEGs significantly associated with EPDS score at week 32 among samples collected during late pregnancy. Gene Set Enrichment Analysis identified immune response and cell motility as processes linked to these DEGs. Hypothesis-based analysis on previously identified postpartum depressive symptoms-related DEGs replicated a positive association between expression of immune-related genes ISG15 and RSAD2 with postpartum-onset depressive symptoms, both in samples taken during late pregnancy and postpartum. The present findings point to transcriptomic signatures associated with peripartum depressive symptoms, mostly related to immune system dysregulation.
围产期抑郁症会对母亲和婴儿的健康产生严重影响。然而,其生物学基础在很大程度上尚不清楚。本研究旨在确定孕期和产后抑郁症状的转录组特征。在妊娠晚期或产后早期采集血样用于mRNA分离和测序,同时使用爱丁堡产后抑郁量表(EPDS)评估抑郁症状。根据样本采集的时间点,通过以下方式鉴定差异表达基因(DEG):(1)比较抑郁症状轨迹组之间的mRNA水平,以及(2)与EPDS评分进行相关性分析。与对照组相比,妊娠晚期而非产后采集的样本中的DEG与仅在孕期出现或产后持续存在的抑郁症状相关。在妊娠晚期采集的样本中,有16个上调和109个下调的DEG在第32周时与EPDS评分显著相关。基因集富集分析确定免疫反应和细胞运动是与这些DEG相关的过程。基于假设对先前确定的产后抑郁症状相关DEG进行的分析,在妊娠晚期和产后采集的样本中均重复了免疫相关基因ISG15和RSAD2的表达与产后发作的抑郁症状之间的正相关。本研究结果指出了与围产期抑郁症状相关的转录组特征,主要与免疫系统失调有关。