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肠道微生物群中某属细菌丰度的降低可能与中国东部女性子痫前期的进展有关。

Decrease in abundance of bacteria of the genus in gut microbiota may be related to pre-eclampsia progression in women from East China.

作者信息

Miao Tingting, Yu Yun, Sun Jin, Ma Aiguo, Yu Jinran, Cui Mengjun, Yang Liping, Wang Huiyan

机构信息

Department of Education, Changzhou Maternity and Child Health Care Hospital Affiliated to Nanjing Medical University, Changzhou, China.

Institute of Nutrition and Health, Qingdao University, Qingdao, China.

出版信息

Food Nutr Res. 2021 Jun 28;65. doi: 10.29219/fnr.v65.5781. eCollection 2021.

Abstract

BACKGROUND

Pre-eclampsia (PE) can result in severe damage to maternal and fetal health. It has been reported that gut microbiota (GM) had important roles in regulating the metabolic and inflammatory responses of the mother. However, investigations on GM in PE are rare.

OBJECTIVE

The objective of the present study was to investigate the changes of GM in PE and how to alter the GM composition in PE by dietary or dietary supplements.

DESIGN

We analyzed the composition changes in GM as well as the relationship between bacteria of different genera and clinical indices by amplifying the V4 region of the 16S ribosomal RNA gene in 12 PE patients and eight healthy pregnant women in East China.

RESULTS

In the PE group, the Observed Species Index was lower than that in the control group, indicating that the α-diversity of the microbiome in the PE group decreased. At phylum, family, and genus levels, the relative abundance of different bacteria in PE patients displayed substantial differences to those from healthy women. We noted a decreased abundance of bacteria of the phylum Actinobacteria ( = 0.042), decreased abundance of bacteria of the family Bifidobacteriaceae ( = 0.039), increased abundance of bacteria of the genus ( = 0.026) and ( = 0.048), and decreased abundance of bacteria of the genus ( = 0.038) Among three enriched genera, bacteria of the genus showed a negative correlation with the systolic blood pressure (SBP), diastolic blood pressure (DBP), and dyslipidemia, which involved glucose metabolism, lipid metabolism, and the oxidative-phosphorylation pathway. The increased abundance of bacteria of the genera and was positively correlated with obesity and dyslipidemia, which involved lipid metabolism, glycosyltransferases, biotin metabolism, and the oxidative-phosphorylation pathways. Moreover, women in the PE group ate more than women in the control group, so fetuses were more prone to overnutrition in the PE group.

CONCLUSION

There is a potential for GM dysbiosis in PE patients, and they could be prone to suffer from metabolic syndrome. We speculate that alterations in the abundance of bacteria of certain genera (e.g. increased abundance of and , and decreased abundance of ) were associated with PE development to some degree. Our data could help to monitor the health of pregnant women and may be helpful for preventing and assisting treatment of PE by increasing dietary fiber or probiotics supplement.

摘要

背景

子痫前期(PE)可导致母婴健康严重受损。据报道,肠道微生物群(GM)在调节母亲的代谢和炎症反应中起重要作用。然而,关于PE中GM的研究很少。

目的

本研究的目的是调查PE中GM的变化,以及如何通过饮食或膳食补充剂改变PE中的GM组成。

设计

我们通过扩增华东地区12例PE患者和8例健康孕妇的16S核糖体RNA基因的V4区域,分析了GM的组成变化以及不同属细菌与临床指标之间的关系。

结果

在PE组中,观察到的物种指数低于对照组,表明PE组中微生物群的α多样性降低。在门、科和属水平上,PE患者中不同细菌的相对丰度与健康女性存在显著差异。我们注意到放线菌门细菌的丰度降低(=0.042),双歧杆菌科细菌的丰度降低(=0.039),某属细菌的丰度增加(=0.026)和某属细菌的丰度增加(=0.我们注意到放线菌门细菌的丰度降低(=0.042),双歧杆菌科细菌的丰度降低(=0.039),某属细菌的丰度增加(=0.026)和某属细菌的丰度增加(=0.048),以及某属细菌的丰度降低(=0.038)。在三个富集属中,某属细菌与收缩压(SBP)、舒张压(DBP)和血脂异常呈负相关,涉及葡萄糖代谢、脂质代谢和氧化磷酸化途径。某属和某属细菌丰度的增加与肥胖和血脂异常呈正相关,涉及脂质代谢、糖基转移酶、生物素代谢和氧化磷酸化途径。此外,PE组女性的食量大于对照组女性,因此PE组胎儿更容易出现营养过剩。

结论

PE患者存在GM失调的可能性,且可能易患代谢综合征。我们推测某些属细菌丰度的改变(如某属和某属丰度增加,某属丰度降低)在一定程度上与PE的发生有关。我们的数据有助于监测孕妇的健康状况,可能有助于通过增加膳食纤维或补充益生菌来预防和辅助治疗PE。 048),以及某属细菌的丰度降低(=0.038)。在三个富集属中,某属细菌与收缩压(SBP)、舒张压(DBP)和血脂异常呈负相关,涉及葡萄糖代谢、脂质代谢和氧化磷酸化途径。某属和某属细菌丰度的增加与肥胖和血脂异常呈正相关,涉及脂质代谢、糖基转移酶、生物素代谢和氧化磷酸化途径。此外,PE组女性的食量大于对照组女性,因此PE组胎儿更容易出现营养过剩。

结论

PE患者存在GM失调的可能性,且可能易患代谢综合征。我们推测某些属细菌丰度的改变(如某属和某属丰度增加,某属丰度降低)在一定程度上与PE的发生有关。我们的数据有助于监测孕妇的健康状况,可能有助于通过增加膳食纤维或补充益生菌来预防和辅助治疗PE。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6591/8254465/35226c2fb95d/FNR-65-5781-g001.jpg

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