Development of a Urine Metabolomics Biomarker-Based Prediction Model for Preeclampsia during Early Pregnancy.
Yaqi ZhangKarl G SylvesterBo JinRonald J WongJames SchillingC James ChouZhi HanRuben Yiqi LuoLu TianSubhashini LadellaLihong MoIvana MarićYair J BlumenfeldGary L DarmstadtGary M ShawDavid K StevensonJohn C WhitinHarvey J CohenDoff B McElhinneyXuefeng B LingPublished in: Metabolites (2023)
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.
Keyphrases
- mass spectrometry
- liquid chromatography
- pregnant women
- low dose
- pregnancy outcomes
- high resolution
- high performance liquid chromatography
- gas chromatography
- high resolution mass spectrometry
- healthcare
- capillary electrophoresis
- tandem mass spectrometry
- cardiovascular events
- early onset
- physical activity
- machine learning
- simultaneous determination
- deep learning
- single cell
- solid phase extraction
- atrial fibrillation
- cardiovascular disease
- multiple sclerosis
- ms ms
- percutaneous coronary intervention
- antiplatelet therapy