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Risk Prediction Model of Early-Onset Preeclampsia Based on Risk Factors and Routine Laboratory Indicators
Yuting Xue1, Nan Yang2, Xunke Gu3
1Department of Laboratory Medicine, Peking University Third Hospital, Beijing 100191, China.
Insights
Early-onset preeclampsia prediction is improved by combining clinical risk factors with routine laboratory indicators. The Support Vector Machine (SVM) model demonstrated superior performance in early detection of early-onset preeclampsia.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Biomedical Data Science
Background:
- Preeclampsia accounts for 10-15% of global maternal deaths.
- Early-onset preeclampsia (PE) presents higher morbidity and mortality than late-onset PE.
- Effective early prediction models for early-onset PE are crucial for improving maternal outcomes.
Purpose of the Study:
- To develop an early-onset preeclampsia prediction model.
- To evaluate the efficacy of clinical characteristics, risk factors, and routine laboratory indicators.
- To compare the performance of logistic regression, decision tree, and Support Vector Machine (SVM) models.
Main Methods:
- Retrospective analysis of 91 early-onset PE patients and 709 controls (January 2010-May 2021).
- Inclusion of clinical characteristics, 12 risk factors, and 38 routine laboratory indicators (blood lipids, liver/kidney function, etc.) from 6-10 weeks gestation.
- Application of logistic regression, decision tree, and SVM models for prediction, with ROC curve analysis (AUC, sensitivity, specificity).
Main Results:
- Significant differences in risk factors (diabetes, APS, kidney disease, OSAHS, primiparity, prior PE, ART) between groups (p < 0.05).
- Most of the 38 routine laboratory indicators showed statistically significant differences (p < 0.05) between early-onset PE and controls.
- Models combining 12 risk factors and 38 laboratory indicators achieved higher AUCs: SVM (0.93), logistic regression (0.86), decision tree (0.77).
Conclusions:
- Clinical risk factors alone have limited efficacy in predicting early-onset PE.
- Combining clinical risk factors with routine laboratory indicators significantly enhances prediction efficacy.
- The SVM model demonstrated superior performance for early prediction of early-onset preeclampsia incidence compared to logistic regression and decision tree models.
Abstract:
Background: Globally, 10-15% of maternal deaths are statistically attributable to preeclampsia. Compared with late-onset PE, the severity of early-onset PE remains more harmful with higher morbidity and mortality. Objective: To establish an early-onset preeclampsia prediction model by clinical characteristics, risk factors and routine laboratory indicators were investigated from pregnant women at 6 to 10 gestational weeks. Methods: The clinical characteristics, risk factors, and 38 routine laboratory indicators (6-10 weeks of gestation) including blood lipids, liver and kidney function, coagulation, blood count, and other indicators of 91 early-onset preeclampsia patients and 709 normal controls without early-onset preeclampsia from January 2010 to May 2021 in Peking University Third Hospital (PUTH) were retrospectively analyzed. A logistic regression, decision tree model, and support vector machine (SVM) model were applied for establishing prediction models, respectively. ROC curves were drawn; area under curve (AUCROC), sensitivity, and specificity were calculated and compared. Results: There were statistically significant differences in the rates of diabetes, antiphospholipid syndrome (APS), kidney disease, obstructive sleep apnea (OSAHS), primipara, history of preeclampsia, and assisted reproductive technology (ART) (p < 0.05). Among the 38 routine laboratory indicators, there were no significant differences in the levels of PLT/LYM, NEU/LYM, TT, D-Dimer, FDP, TBA, ALP, TP, ALB, GLB, UREA, Cr, P, Cystatin C, HDL-C, Apo-A1, and Lp(a) between the two groups (p > 0.05). The levels of the rest indicators were all statistically different between the two groups (p < 0.05). If only 12 risk factors of PE were analyzed with the logistic regression, decision tree model, and support vector machine (SVM), and the AUCROC were 0.78, 0.74, and 0.66, respectively, while 12 risk factors of PE and 38 routine laboratory indicators were analyzed with the logistic regression, decision tree model, and support vector machine (SVM), and the AUCROC were 0.86, 0.77, and 0.93, respectively. Conclusions: The efficacy of clinical risk factors alone in predicting early-onset preeclampsia is not high while the efficacy increased significantly when PE risk factors combined with routine laboratory indicators. The SVM model was better than logistic regression model and decision tree model in early prediction of early-onset preeclampsia incidence.
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