A machine learning model predicts risk of Down syndrome and related defects using maternal factors and ultrasound, suggesting potential for personalized care.
This study developed a machine learning model for early risk stratification of Down syndrome by integrating maternal serum biomarkers and ultrasound measurements. A retrospective multicentre dataset was used, including maternal age, AFP, HCG, INHIBIN-A, and ultrasound parameters (NT, CRL). After imputing missing data and engineering features (e.g., Age_NT_interaction), a Gradient Boosting Machine (GBM) was trained and evaluated using AUROC, precision, recall, and F1-score. The model achieved high performance (AUROC: 0.9921; precision: 1.00; F1-score: 0.91; accuracy: 0.97). SHAP analysis identified key interactions—particularly Age_NT, Age_HCG, and Age_PAPP-A—as major contributors. High maternal age combined with elevated HCG or low PAPP-A was linked to increased risk, aligning with clinical knowledge. The model offers a highly accurate and interpretable approach for Down syndrome risk prediction, supporting personalized, data-driven prenatal care. Prospective validation and clinical integration are recommended.
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Sadegh‐Zadeh et al. (2025) studied this question.
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