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Updated: May 7, 2026

One-step Metabolomics: Carbohydrates, Organic and Amino Acids Quantified in a Single Procedure
Published on: June 25, 2010
Active metabolomics identify potential functional metabolites for preeclampsia prevention
Zhongxiao Zhang1, Ping He2, Danni Chen2
1Department of Gynaecology and Obstetrics, Tongren Hospital, Shanghai Jiaotong University School of Medicine, 1111XianXia Road, Shanghai 200336, China; Hongqiao International Institute of Medicine, Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Preeclampsia (PE) is linked to altered blood metabolites. The study found that LysoPE(16:0) is reduced in PE and may protect against it by influencing the GSK-3β/β-Catenin pathway.
Area of Science:
- Metabolomics
- Biochemistry
- Obstetrics
Background:
- Preeclampsia (PE) is a major cause of maternal and fetal mortality.
- Limited effective treatments exist for PE.
- Metabolomics can identify biomarkers and therapeutic targets for PE.
Purpose of the Study:
- To compare serum metabolomics profiles in preeclampsia and normal pregnancies.
- To investigate the role of LysoPE(16:0) in trophoblast function.
- To explore the molecular mechanisms underlying LysoPE(16:0)'s effects.
Main Methods:
- Untargeted liquid chromatography-mass spectrometry (LC-MS) metabolomics.
- Analysis of serum samples from PE patients and controls.
- Functional assays on trophoblast cells and mechanistic studies involving GSK-3β.
Main Results:
- Significant alterations in lysophosphatidylcholines and organic acids were observed.
- LysoPE(16:0) was downregulated in PE serum.
- LysoPE(16:0) promoted trophoblast cell invasion and migration, potentially via GSK-3β/β-Catenin pathway modulation.
Conclusions:
- LysoPE(16:0) plays a role in PE pathophysiology.
- LysoPE(16:0) may be a therapeutic target or biomarker for PE.
- Modulation of the GSK-3β/β-Catenin pathway by LysoPE(16:0) offers new insights into PE treatment.
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