Center for Women's and Children's Health and Metabolism Research, Wuhan University School of Nursing, Wuhan University, 169 Donghu Road, Wuhan, 430071, China.
Emory University Nell Hodgson Woodruff School of Nursing, 1520 Clifton Road, Atlanta, GA, 30322, USA.
J Psychiatr Res. 2023 Aug;164:458-467. doi: 10.1016/j.jpsychires.2023.06.034. Epub 2023 Jul 6.
The mechanism of levels of inflammatory cytokines that affects brain function and mood through gut microbiota has not been fully elucidated. This study aimed to investigate the potential mediating role of gut microbiota between maternal inflammatory cytokines levels and prenatal depression.
There were 29 women in the prenatal depression group and 27 women in the control group enrolled in this study. The Edinburgh Postnatal Depression Scale (EPDS) score of 10 was considered the cut-off value for prenatal depression. We collected demographic information, stool and blood samples. The gut microbiota was profiled using V3-V4 gene sequence of 16S rRNA, and the concentration of inflammatory cytokines were analyzed. The mediation model was analyzed by using the model 4 in the process procedure for SPSS.
There were significance differences in the concentration of interleukin-1beta (IL-1β)(Z = -2.383, P = 0.017) and IL-17A (Z = -2.439, P = 0.015) between the prenatal depression group and control group. There was no significant difference in α- diversity and β-diversity between the two groups. Intestinibacter (OR: 0.012; 95% CI, 0.001-0.195) and Escherichia_Shigella (OR: 0.103; 95% CI, 0.014-0.763) were protective factors for prenatal depression, while Tyzzerella (OR: 17.941; 95% CI, 1.764-182.445) and Unclassified_f_Ruminococcaceae (OR: 22.607; 95% CI, 1.242-411.389) were risk factors. And Intestinibacter play a mediation effect between IL-17A and prenatal depression.
Maternal gut microbiota is a significant mediator of the relationship between inflammatory cytokines and prenatal depression. Further research is still needed in exploring the mediating mechanisms of gut microbiota between inflammatory cytokines and depression.
炎症细胞因子通过肠道微生物群影响大脑功能和情绪的机制尚未完全阐明。本研究旨在探讨肠道微生物群在母体炎症细胞因子水平与产前抑郁之间的潜在中介作用。
本研究纳入了 29 名产前抑郁组和 27 名对照组的女性。以 EPDS 评分≥10 为产前抑郁的截断值。我们收集了人口统计学信息、粪便和血液样本。使用 16S rRNA V3-V4 基因序列对肠道微生物群进行了分析,并检测了炎症细胞因子的浓度。使用 SPSS 过程程序中的模型 4 分析了中介模型。
产前抑郁组和对照组之间白细胞介素-1β(IL-1β)(Z=-2.383,P=0.017)和 IL-17A(Z=-2.439,P=0.015)的浓度存在显著差异。两组之间的 α 多样性和 β 多样性无显著差异。肠杆菌属(OR:0.012;95%CI,0.001-0.195)和埃希氏菌-志贺氏菌(OR:0.103;95%CI,0.014-0.763)是产前抑郁的保护因素,而 Tyzzerella(OR:17.941;95%CI,1.764-182.445)和未分类_f_Ruminococcaceae(OR:22.607;95%CI,1.242-411.389)是风险因素。肠杆菌属在 IL-17A 与产前抑郁之间发挥了中介作用。
母体肠道微生物群是炎症细胞因子与产前抑郁之间关系的重要中介。需要进一步研究探索肠道微生物群在炎症细胞因子与抑郁之间的中介机制。