Department of Psychology, Queens College, CUNY, Flushing, New York, United States.
Department of Psychology, The Graduate Center, CUNY, Graduate School of Public Health, New York, NY, USA.
Mol Psychiatry. 2021 Nov;26(11):6520-6530. doi: 10.1038/s41380-021-01123-z. Epub 2021 May 12.
Prenatal stress can lead to long-term adverse effects that increase the risk of anxiety and other emotional disorders in offspring. The in utero underpinnings contributing to such phenotypes remain unknown. We profiled the transcriptome of placental specimens from women who lived through Hurricane Sandy during pregnancy compared to those pregnant during non-Sandy conditions. Following birth, longitudinal assessments were conducted in their offspring during childhood (~3-4 years old) to measure steroid hormones (in hair) and behavioral and emotional problems. This revealed a significant link between prenatal Sandy stress (PNSS) and child HPA dysfunction, evident by altered cortisol, dehydroepiandrosterone (DHEA), and cortisol:DHEA levels. In addition, PNSS was associated with significantly increased anxiety and aggression. These findings coincided with significant reorganization of the placental transcriptome via vascular, immune, and endocrine gene pathways. Interestingly, many of the most prominently altered genes were known to be uniquely expressed in syncytiotrophoblast (STB)-subtype of placental cells and harbored glucocorticoid response elements in promoter regions. Finally, several vascular development- and immune-related placental gene sets were found to mediate the relationship between PNSS and childhood phenotypes. Overall, these findings suggest that natural disaster-related stress during pregnancy reprograms the placental molecular signature, potentially driving long-lasting changes in stress regulation and emotional health. Further examination of placental mechanisms may elucidate the environment's contribution to subsequent risk for anxiety disorders later in life.
产前应激可导致长期的不良影响,增加后代焦虑和其他情绪障碍的风险。导致这种表型的子宫内基础仍然未知。我们对经历过桑迪飓风的孕妇和非桑迪条件下孕妇的胎盘标本进行了转录组分析。分娩后,对其后代进行了纵向评估,以测量皮质醇(头发中的)和行为及情绪问题。这表明产前桑迪应激(PNSS)与儿童 HPA 功能障碍之间存在显著联系,这表现为皮质醇、脱氢表雄酮(DHEA)和皮质醇:DHEA 水平的改变。此外,PNSS 与焦虑和攻击性的显著增加有关。这些发现与胎盘转录组通过血管、免疫和内分泌基因途径的显著重排相吻合。有趣的是,许多变化最明显的基因被认为是胎盘细胞合胞滋养层(STB)亚型中特有的,并且在启动子区域中具有糖皮质激素反应元件。最后,发现几个与血管发育和免疫相关的胎盘基因集介导了 PNSS 与儿童表型之间的关系。总的来说,这些发现表明,怀孕期间与自然灾害相关的应激会重新编程胎盘的分子特征,可能导致应激调节和情绪健康的持久变化。进一步研究胎盘机制可能阐明环境对以后生活中焦虑障碍风险的贡献。