The First Affiliated Hospital of Jinan University, Guangzhou, China.
Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, China.
Front Cell Infect Microbiol. 2019 Jun 26;9:224. doi: 10.3389/fcimb.2019.00224. eCollection 2019.
Imbalances in gut microbiota composition are linked to hypertension, host metabolic abnormalities, systemic inflammation, and other conditions. In the present study, we examined the changes of gut microbiota in women with early-onset preeclampsia (PE) and in normotensive, uncomplicated pregnant women during late pregnancy and at 1 and 6 weeks postpartum. Gut microbiota profiles of women with PE and healthy pregnant women in the third trimester and at 1 and 6 weeks postpartum were assessed by 16S rRNA gene amplicon sequencing. Plasma levels of interleukin-6 (IL-6), intestinal fatty acid-binding protein (I-FABP), zonulin, and lipopolysaccharide (LPS) were measured in the third trimesters. At the genus level, 8 bacterial genera were significantly enriched in the antepartum samples of PE patients compared to healthy controls, of which , and represented the major variances in PE microbiomes. Conversely, 5 genera, including , and , were significantly depleted in antepartum PE samples. Maternal blood pressure and liver enzyme levels were positively correlated to the PE-enriched genera such as , and , while the fetal features (e.g., Apgar score and newborn birth weight) were positively correlated with PE-depleted genera and negatively correlated with PE-enriched genera. Moreover, maternal blood IL-6 level was positively associated with gut and , whereas LPS level was negatively associated with . In terms of postpartum women, both the gut microbial composition and the PE-associated microbial alterations were highly consistent with those of the antepartum women. PE diagnosed in the third trimester of pregnancy is associated with a disrupted gut microbiota composition compared with uncomplicated pregnant women, which are associated with maternal clinical features (blood pressure level and liver dysfunction) and newborn birth weight. Moreover, these antepartum alterations in gut microbiota persisted 6 weeks postpartum.
肠道微生物群落组成的失衡与高血压、宿主代谢异常、全身炎症等有关。本研究旨在探讨早发型子痫前期(PE)患者与正常妊娠、无并发症孕妇在妊娠晚期及产后 1 周和 6 周时肠道微生物群落的变化。采用 16S rRNA 基因扩增子测序法分析 PE 患者和健康孕妇在妊娠晚期、产后 1 周和 6 周时的肠道微生物群。在妊娠晚期测量白细胞介素-6(IL-6)、肠型脂肪酸结合蛋白(I-FABP)、肠紧密连接蛋白(zonulin)和脂多糖(LPS)的血浆水平。在属水平上,与健康对照组相比,8 个细菌属在前瞻性 PE 患者样本中显著富集,其中 、 和 代表 PE 微生物组的主要差异。相反,5 个属,包括 、 和 ,在前瞻性 PE 样本中显著减少。产妇血压和肝酶水平与 PE 富集属如 、 和 呈正相关,而胎儿特征(如阿普加评分和新生儿出生体重)与 PE 耗竭属呈正相关,与 PE 富集属呈负相关。此外,母体血液中 IL-6 水平与肠道 和 呈正相关,而 LPS 水平与 呈负相关。就产后妇女而言,肠道微生物组成和与 PE 相关的微生物改变与产前妇女非常一致。与无并发症孕妇相比,妊娠晚期诊断的 PE 与肠道微生物群落组成紊乱有关,与母体临床特征(血压水平和肝功能障碍)和新生儿出生体重有关。此外,这些产前肠道微生物群落的改变在产后 6 周仍持续存在。