A nomogram based on hematological parameters for prediction of spontaneous abortion risk in pregnancies
- PMID: 40069650
- PMCID: PMC11899064
- DOI: 10.1186/s12884-025-07396-4
A nomogram based on hematological parameters for prediction of spontaneous abortion risk in pregnancies
Abstract
Background: Pregnancy loss significantly affects physical and mental health. A nomogram for predicting spontaneous abortion risk was developed to improve pregnancy outcomes.
Methods: A total of 1346 pregnant women were enrolled from The Third Affiliated Hospital of Wenzhou Medical University (May 2020 - May 2022). The training set included 941 participants, and the validation set had 405. Feature selection was optimized using a random forest model, and a predictive model was constructed via multivariable logistic regression. The nomogram's performance was assessed with receiver operator characteristic (ROC), Hosmer-Lemeshow test, calibration curve, and clinical impact curve (CIC). Discrimination and clinical utility were compared between the nomogram and its individual variables.
Results: Antithrombin III (AT-III), homocysteine (Hcy), complement component 3 (C3), protein C (PC), and anti-β2 glycoprotein I antibody (anti-β2GP1) were identified as risk factors. The nomogram demonstrated satisfactory discrimination (Training AUC: 0.813, 95% CI: 0.790-0.842; Validation AUC: 0.792, 95% CI: 0.741-0.838). The Hosmer-Lemeshow test (P = 0.331) indicated a good fit, and the CIC showed clinical net benefit. The nomogram outperformed individual variables in discrimination (AUC: 0.804, 95% CI: 0.779-0.829).
Conclusion: The developed nomogram, incorporating AT-III, Hcy, C3, PC, and anti-β2GP1, aids clinicians in identifying pregnant women at high risk for spontaneous abortion.
Keywords: Abortion; Hematological parameters; Nomogram; Receiver operator characteristic.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: This study was reviewed and approved by the Ethics Committee of The Third Affiliated Hospital of Wenzhou Medical University. The patients/participants provided written informed consent to participate in this study. Consent for publication: Before participating in the study, all participants signed up with informed permission. Competing interests: The authors declare no competing interests.
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