4.6 Article

Development of a Urine Metabolomics Biomarker-Based Prediction Model for Preeclampsia during Early Pregnancy

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METABOLITES
卷 13, 期 6, 页码 -

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MDPI
DOI: 10.3390/metabo13060715

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early pregnancy; preeclampsia risk prediction; biomarker; urinary metabolite; LC-MS; MS

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This study identified seven metabolomic biomarkers in urine samples collected from 60 pregnant women, using liquid chromatography mass spectrometry (LCMS/MS). A predictive model based on these biomarkers was developed using the XGBoost algorithm and showed good performance in identifying individuals at risk of developing preeclampsia.
Preeclampsia (PE) is a condition that poses a significant risk of maternal mortality and multiple organ failure during pregnancy. Early prediction of PE can enable timely surveillance and interventions, such as low-dose aspirin administration. In this study, conducted at Stanford Health Care, we examined a cohort of 60 pregnant women and collected 478 urine samples between gestational weeks 8 and 20 for comprehensive metabolomic profiling. By employing liquid chromatography mass spectrometry (LCMS/MS), we identified the structures of seven out of 26 metabolomics biomarkers detected. Utilizing the XGBoost algorithm, we developed a predictive model based on these seven metabolomics biomarkers to identify individuals at risk of developing PE. The performance of the model was evaluated using 10-fold cross-validation, yielding an area under the receiver operating characteristic curve of 0.856. Our findings suggest that measuring urinary metabolomics biomarkers offers a noninvasive approach to assess the risk of PE prior to its onset.

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