Department of Psychology, Temple University, Philadelphia, PA, USA.
Cousins Center for Psychoneuroimmunology, Dept. of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, USA.
J Psychiatr Res. 2019 Apr;111:96-103. doi: 10.1016/j.jpsychires.2019.01.009. Epub 2019 Jan 10.
Maternal infection during pregnancy has been associated with increased risk of offspring psychopathology, including depression. As most infections do not cross the placenta, maternal immune responses to infection have been considered as potentially contributing to this relationship. This study examined whether gestational timing of maternal inflammation during pregnancy is associated with offspring internalizing and/or externalizing symptoms during childhood and, further, whether fetal sex moderated this relationship.
Participants were 737 pregnant women and their offspring who were continuously followed through late childhood. Archived first and second trimester sera were analyzed for markers of inflammation [interleukin 8 (IL-8), IL-6, IL-1 receptor antagonist (IL-1ra), and soluble tumor necrosis factor receptor-II (sTNF-RII)]. When offspring were aged 9-11, mothers completed a questionnaire assessing psychological symptoms.
Multivariate regression analyses indicated that elevated IL-8 in the first trimester was associated with significantly higher levels of externalizing symptoms in offspring. Higher IL-1ra in the second trimester was associated with higher offspring internalizing symptoms. Further, second trimester IL-1ra was associated with increased internalizing symptoms in females only.
These findings demonstrate that elevated maternal inflammation during pregnancy is associated with the emergence of separate psychological phenotypes and that timing of exposure and fetal sex matter for offspring outcomes. Given that internalizing and externalizing symptoms in childhood increase risk for a variety of mental disorders later in development, these findings potentially have major implications for early intervention and prevention work.
孕期母体感染与后代精神病理学风险增加相关,包括抑郁。由于大多数感染不会穿过胎盘,因此母体对感染的免疫反应被认为可能与这种关系有关。本研究探讨了孕期母体炎症的孕时是否与后代儿童期的内化和/或外化症状有关,进一步探讨了胎儿性别是否调节了这种关系。
本研究纳入了 737 名孕妇及其后代,这些参与者在整个儿童期都被连续随访。分析了存档的第一和第二孕期血清中炎症标志物[白细胞介素 8(IL-8)、IL-6、IL-1 受体拮抗剂(IL-1ra)和可溶性肿瘤坏死因子受体-II(sTNF-RII)]。当后代年龄为 9-11 岁时,母亲完成了一份评估心理症状的问卷。
多变量回归分析表明,第一孕期 IL-8 升高与后代外化症状水平显著升高相关。第二孕期 IL-1ra 升高与后代内化症状升高相关。此外,第二孕期 IL-1ra 仅与女性后代内化症状增加相关。
这些发现表明,孕期母体炎症升高与特定的心理表型的出现有关,并且暴露时间和胎儿性别对后代结局有影响。鉴于儿童期的内化和外化症状会增加以后发展为各种精神障碍的风险,这些发现可能对早期干预和预防工作具有重要意义。