Kimmel Mary, Tong Bangzhuo, Devall Alfons Edbom, Björvang Richelle D, Schuppe-Koistinen Ina, Engstrand Lars, Fransson Emma, Skalkidou Alkistis, Hugerth Luisa W
Department of Women's and Children's Health, Uppsala University, Uppsala, Sweden.
Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Biol Psychiatry Glob Open Sci. 2025 Jan 30;5(3):100453. doi: 10.1016/j.bpsgos.2025.100453. eCollection 2025 May.
In this study, we aimed to characterize the gut microbiome and its potential functioning in 2 populations at 2 time points during pregnancy in relation to mental distress.
During the second and third trimester, individuals from the United States and Sweden completed the Edinburgh Postnatal Depression Scale and provided fecal samples for whole-genome metagenomics. A total of 832 and 161 samples were sequenced and analyzed from the Swedish cohort and the U.S. cohort, respectively. Multiple characterizations of the microbial community were analyzed in relation to distress measured using the Edinburgh Postnatal Depression Scale. Principal coordinate analysis and distance-based redundancy analysis assessed variation in functional gut-brain modules. For the U.S. cohort, the Trier Social Stress Test was administered 8 weeks postpartum while collecting salivary cortisol.
Principal coordinate analysis identified 4 sample clusters based on the gut-brain modules distinguished by functions such as short-chain fatty acid synthesis and cortisol degradation. While with distance-based redundancy analysis, mental distress subtypes did not significantly contribute to variation in gut-brain modules ( = .085 for Sweden, = .23 for the U.S.), a U.S. sample cluster distinguished by lower cortisol degradation from another cluster with higher gut microbial cortisol degradation abundance had significantly higher odds of being associated with depression ( = .024). The U.S. sample cluster with lower gut microbial cortisol degradation abundance also had significantly higher cortisol levels after a postpartum social stressor.
Further studies are warranted to investigate the potential for the gut microbiome to serve as biomarkers of gut-brain axis health during pregnancy across disparate populations.
在本研究中,我们旨在描述孕期两个时间点两个群体的肠道微生物群及其与精神困扰相关的潜在功能。
在妊娠中期和晚期,来自美国和瑞典的个体完成了爱丁堡产后抑郁量表,并提供粪便样本用于全基因组宏基因组学分析。分别对瑞典队列和美国队列的832份和161份样本进行了测序和分析。针对使用爱丁堡产后抑郁量表测量的精神困扰,分析了微生物群落的多种特征。主坐标分析和基于距离的冗余分析评估了功能性肠脑模块的变化。对于美国队列,在产后8周进行了特里尔社会应激测试,同时收集唾液皮质醇。
主坐标分析根据短链脂肪酸合成和皮质醇降解等功能区分的肠脑模块,确定了4个样本簇。虽然基于距离的冗余分析显示,精神困扰亚型对肠脑模块的变化没有显著贡献(瑞典:P = 0.085;美国:P = 0.23),但美国一个以较低皮质醇降解为特征的样本簇与另一个肠道微生物皮质醇降解丰度较高的样本簇相比,与抑郁症相关的几率显著更高(P = 0.024)。美国肠道微生物皮质醇降解丰度较低的样本簇在产后社会应激源后皮质醇水平也显著更高。
有必要进一步研究肠道微生物群在不同人群孕期作为肠脑轴健康生物标志物的潜力。