Gut microbiota interacting with vitamin D but not anandamide might contribute to the pathogenesis of preeclampsia: a preliminary study

IntroductionPreeclampsia (PE) is a pregnancy-specific multisystem disorder and a leading cause of maternal and perinatal mortality globally. Despite numerous studies highlighting the potential roles of gut microbiota, anandamide (AEA), and Vitamin D (VitD) in PE, none have established them as reliab...

Full description

Saved in:
Bibliographic Details
Main Authors: Xiao-Qiang Han, Hui-Hui Jiang, Meng-Ling Chen, De-Yang Han, Su-Fen Zhou, Jin-Wen Wang, Shu-Shen Ji, Ling-Yun Wang, Jing-Wei Lou, Ming-Qun Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-02-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcimb.2024.1469054/full
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832539873984118784
author Xiao-Qiang Han
Xiao-Qiang Han
Hui-Hui Jiang
Meng-Ling Chen
Meng-Ling Chen
De-Yang Han
De-Yang Han
Su-Fen Zhou
Su-Fen Zhou
Jin-Wen Wang
Shu-Shen Ji
Ling-Yun Wang
Jing-Wei Lou
Ming-Qun Li
Ming-Qun Li
author_facet Xiao-Qiang Han
Xiao-Qiang Han
Hui-Hui Jiang
Meng-Ling Chen
Meng-Ling Chen
De-Yang Han
De-Yang Han
Su-Fen Zhou
Su-Fen Zhou
Jin-Wen Wang
Shu-Shen Ji
Ling-Yun Wang
Jing-Wei Lou
Ming-Qun Li
Ming-Qun Li
author_sort Xiao-Qiang Han
collection DOAJ
description IntroductionPreeclampsia (PE) is a pregnancy-specific multisystem disorder and a leading cause of maternal and perinatal mortality globally. Despite numerous studies highlighting the potential roles of gut microbiota, anandamide (AEA), and Vitamin D (VitD) in PE, none have established them as reliable biomarkers for predicting disease onset. Moreover, their interactions in late-stage pregnancy women remain poorly understood.MethodsThirty-four preeclamptic patients (called PE group) and thirty-nine matched healthy late-pregnant women (called LP group) were involved in this case-control study. Fecal samples, which were used to acquire the diversity and composition of gut microbiota, were analyzed by 16S rRNA gene sequencing. Plasma AEA concentrations and serum VitD levels were determined by high-performance liquid chromatography-mass spectrometry (HPLC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS), respectively.ResultsIn this study, β diversity but not α diversity significantly differed between the LP and PE groups. Compared with the LP group, the relative abundances of Prevotella, Erysipelotrichaceae_UCG-003, and Dorea were increased dramatically in the PE group, whereas the relative abundances of Subdoligranulum, Parabacteroides, Bacteroides were significantly decreased in the PE group. Furthermore, women with PE had a substantially lower plasma level of AEA and a marked decrease in serum VitD compared to normal late-pregnant women. Lastly, although the serum level of AEA was not significantly correlated with VitD or any of the top 6 marker genera, VitD was significantly negatively correlated with the relative abundance of Dorea, a novel finding in this context.DiscussionThe gut microbiota profile of the PE group was significantly different from that of the LP group. Although no significant correlations were identified between the plasma AEA levels and serum VitD levels or any of the top 6 identified marker genera, a significant negative correlation was observed between VitD and Dorea, indicating VitD and gut microbiota have the potential to be combined targets for early diagnosis and management of PE.
format Article
id doaj-art-1758ec20d2f741069044ef4edf94e3f7
institution Kabale University
issn 2235-2988
language English
publishDate 2025-02-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Cellular and Infection Microbiology
spelling doaj-art-1758ec20d2f741069044ef4edf94e3f72025-02-05T07:32:37ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882025-02-011410.3389/fcimb.2024.14690541469054Gut microbiota interacting with vitamin D but not anandamide might contribute to the pathogenesis of preeclampsia: a preliminary studyXiao-Qiang Han0Xiao-Qiang Han1Hui-Hui Jiang2Meng-Ling Chen3Meng-Ling Chen4De-Yang Han5De-Yang Han6Su-Fen Zhou7Su-Fen Zhou8Jin-Wen Wang9Shu-Shen Ji10Ling-Yun Wang11Jing-Wei Lou12Ming-Qun Li13Ming-Qun Li14Department of Obstetrics and Gynaecology, Xiangyang No. 1 People’s Hospital, Hubei University of Medicine, Xiangyang, ChinaHubei Provincial Clinical Research Center for Accurate Fetus Malformation Diagnosis, Xiangyang, ChinaZhangjiang Center for Translational Medicine, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, ChinaDepartment of Obstetrics and Gynaecology, Xiangyang No. 1 People’s Hospital, Hubei University of Medicine, Xiangyang, ChinaHubei Provincial Clinical Research Center for Accurate Fetus Malformation Diagnosis, Xiangyang, ChinaDepartment of Obstetrics and Gynaecology, Xiangyang No. 1 People’s Hospital, Hubei University of Medicine, Xiangyang, ChinaHubei Provincial Clinical Research Center for Accurate Fetus Malformation Diagnosis, Xiangyang, ChinaHubei Provincial Clinical Research Center for Accurate Fetus Malformation Diagnosis, Xiangyang, ChinaDepartment of Ultrasound, Xiangyang No. 1 People’s Hospital, Hubei University of Medicine, Xiangyang, ChinaZhangjiang Center for Translational Medicine, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, ChinaZhangjiang Center for Translational Medicine, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, ChinaZhangjiang Center for Translational Medicine, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, ChinaZhangjiang Center for Translational Medicine, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, ChinaDepartment of Obstetrics and Gynaecology, Xiangyang No. 1 People’s Hospital, Hubei University of Medicine, Xiangyang, ChinaHubei Provincial Clinical Research Center for Accurate Fetus Malformation Diagnosis, Xiangyang, ChinaIntroductionPreeclampsia (PE) is a pregnancy-specific multisystem disorder and a leading cause of maternal and perinatal mortality globally. Despite numerous studies highlighting the potential roles of gut microbiota, anandamide (AEA), and Vitamin D (VitD) in PE, none have established them as reliable biomarkers for predicting disease onset. Moreover, their interactions in late-stage pregnancy women remain poorly understood.MethodsThirty-four preeclamptic patients (called PE group) and thirty-nine matched healthy late-pregnant women (called LP group) were involved in this case-control study. Fecal samples, which were used to acquire the diversity and composition of gut microbiota, were analyzed by 16S rRNA gene sequencing. Plasma AEA concentrations and serum VitD levels were determined by high-performance liquid chromatography-mass spectrometry (HPLC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS), respectively.ResultsIn this study, β diversity but not α diversity significantly differed between the LP and PE groups. Compared with the LP group, the relative abundances of Prevotella, Erysipelotrichaceae_UCG-003, and Dorea were increased dramatically in the PE group, whereas the relative abundances of Subdoligranulum, Parabacteroides, Bacteroides were significantly decreased in the PE group. Furthermore, women with PE had a substantially lower plasma level of AEA and a marked decrease in serum VitD compared to normal late-pregnant women. Lastly, although the serum level of AEA was not significantly correlated with VitD or any of the top 6 marker genera, VitD was significantly negatively correlated with the relative abundance of Dorea, a novel finding in this context.DiscussionThe gut microbiota profile of the PE group was significantly different from that of the LP group. Although no significant correlations were identified between the plasma AEA levels and serum VitD levels or any of the top 6 identified marker genera, a significant negative correlation was observed between VitD and Dorea, indicating VitD and gut microbiota have the potential to be combined targets for early diagnosis and management of PE.https://www.frontiersin.org/articles/10.3389/fcimb.2024.1469054/fullgut microbiotaanandamidevitamin Dpreeclampsiainflammationinteraction
spellingShingle Xiao-Qiang Han
Xiao-Qiang Han
Hui-Hui Jiang
Meng-Ling Chen
Meng-Ling Chen
De-Yang Han
De-Yang Han
Su-Fen Zhou
Su-Fen Zhou
Jin-Wen Wang
Shu-Shen Ji
Ling-Yun Wang
Jing-Wei Lou
Ming-Qun Li
Ming-Qun Li
Gut microbiota interacting with vitamin D but not anandamide might contribute to the pathogenesis of preeclampsia: a preliminary study
Frontiers in Cellular and Infection Microbiology
gut microbiota
anandamide
vitamin D
preeclampsia
inflammation
interaction
title Gut microbiota interacting with vitamin D but not anandamide might contribute to the pathogenesis of preeclampsia: a preliminary study
title_full Gut microbiota interacting with vitamin D but not anandamide might contribute to the pathogenesis of preeclampsia: a preliminary study
title_fullStr Gut microbiota interacting with vitamin D but not anandamide might contribute to the pathogenesis of preeclampsia: a preliminary study
title_full_unstemmed Gut microbiota interacting with vitamin D but not anandamide might contribute to the pathogenesis of preeclampsia: a preliminary study
title_short Gut microbiota interacting with vitamin D but not anandamide might contribute to the pathogenesis of preeclampsia: a preliminary study
title_sort gut microbiota interacting with vitamin d but not anandamide might contribute to the pathogenesis of preeclampsia a preliminary study
topic gut microbiota
anandamide
vitamin D
preeclampsia
inflammation
interaction
url https://www.frontiersin.org/articles/10.3389/fcimb.2024.1469054/full
work_keys_str_mv AT xiaoqianghan gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT xiaoqianghan gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT huihuijiang gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT menglingchen gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT menglingchen gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT deyanghan gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT deyanghan gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT sufenzhou gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT sufenzhou gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT jinwenwang gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT shushenji gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT lingyunwang gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT jingweilou gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT mingqunli gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy
AT mingqunli gutmicrobiotainteractingwithvitamindbutnotanandamidemightcontributetothepathogenesisofpreeclampsiaapreliminarystudy