Development and validation of a predictive model for preeclampsia: a retrospective cohort study
- PMID: 40450650
- DOI: 10.1007/s00404-025-08076-6
Development and validation of a predictive model for preeclampsia: a retrospective cohort study
Abstract
Purpose: We conduct this study to develop and validate a predictive nomogram for preeclampsia (PE) to inform the development of early intervention strategies in clinical practice.
Methods: In this analysis, we collected data from women with medium or high risk for PE who underwent placental growth factor (PlGF)-based testing between December 20, 2021 and December 31, 2022. The gestational age at the time of taking the PlGF-based test for the PE and non-PE groups was 20.0 weeks (range 16.1-26.1 weeks) and 22.2 weeks (range 16.2-27.3 weeks), respectively. The independent risk factors for PE were identified through both univariate and multivariate analyses. Based on these independent risk factors, a logistic regression model for risk prediction was developed. The model was validated using five-fold cross-validation. Moreover, the efficacy of the model was appraised using the area under the receiver operating characteristic curve (AUROC), while the calibration of the model was assessed through calibration curves. Additionally, decision curves and clinical impact curves were leveraged to evaluate the clinical applicability of the model.
Results: In total, 2063 women were included. Of these, 108 had PE. Body mass index, mean arterial pressure, a ratio of soluble fms-like tyrosine kinase-1/PlGF, history of adverse pregnancy, family history of PE, previous history of PE, chronic hypertension, autoimmune disease, and polycystic ovary syndrome were independent risk factors for PE. The model constructed based on independent risk factors demonstrated that the AUROC in the training set was 0.883 (95% confidence interval [CI] 0.838-0.928), with a sensitivity of 0.827 and specificity of 0.816. In the validation set, the AUROC was 0.862 (95% CI 0.774-0.951), with a sensitivity of 0.815 and specificity of 0.772. The decision curve revealed that the model had a large probability interval for the net benefit threshold.
Conclusion: The predictive nomogram for PE constructed based on common interpretable features has desirable efficacy, which informs the development of specialized preventive protocols in clinical practice.
Keywords: Nomogram; Placental growth factor; Preeclampsia; Soluble fms-like tyrosine kinase-1.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Conflict of interest: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. Ethical approval: The dataset of this retrospective study was from patient’s electronic medical records. Written consent was obtained from all the participants. The study protocol was approved by the Science Research Ethics Committee, Linyi People’s Hospital (YX200683). Declaration of generative AI in scientific writing: The authors did not use generative AI or AI-assisted technologies in the development of this manuscript.
Similar articles
-
Development and validation of a preeclampsia prediction model for the first and second trimester pregnancy based on medical history.BMC Pregnancy Childbirth. 2025 May 27;25(1):616. doi: 10.1186/s12884-025-07733-7. BMC Pregnancy Childbirth. 2025. PMID: 40426100 Free PMC article.
-
Pre-pregnancy body mass index combined with peripheral blood PLGF, DCN, LDH, and UA in a risk prediction model for pre-eclampsia.Front Endocrinol (Lausanne). 2024 Jan 8;14:1297731. doi: 10.3389/fendo.2023.1297731. eCollection 2023. Front Endocrinol (Lausanne). 2024. PMID: 38260145 Free PMC article.
-
Angiogenic markers and their longitudinal change for predicting adverse outcomes in pregnant women with chronic hypertension.Am J Obstet Gynecol. 2021 Sep;225(3):305.e1-305.e14. doi: 10.1016/j.ajog.2021.03.041. Epub 2021 Apr 1. Am J Obstet Gynecol. 2021. PMID: 33812812
-
A dynamic prediction model for preeclampsia using the sFlt-1/PLGF ratio combined with multiple factors.BMC Pregnancy Childbirth. 2024 Jun 26;24(1):443. doi: 10.1186/s12884-024-06627-4. BMC Pregnancy Childbirth. 2024. PMID: 38926668 Free PMC article.
-
Predictive value of the soluble fms-like tyrosine kinase 1 to placental growth factor ratio for preeclampsia in twin pregnancies: a systematic review and meta-analysis.Am J Obstet Gynecol MFM. 2024 Mar;6(3):101290. doi: 10.1016/j.ajogmf.2024.101290. Epub 2024 Feb 23. Am J Obstet Gynecol MFM. 2024. PMID: 38401234
References
-
- Kassebaum NJ, Barber RM, Bhutta ZA, Dandona L, Gething PW, Hay SI, Kinfu Y, Larson HJ, Liang X, Lim SS, Lopez AD (2016) Global, regional, and national levels of maternal mortality, 1990–2015: a systematic analysis for the global burden of disease study 2015. Lancet 388(10053):1775–812. https://doi.org/10.1016/s0140-6736(16)31470-2 - DOI
-
- Poon LC, Shennan A, Hyett JA, Kapur A, Hadar E, Divakar H et al (2019) The international federation of gynecology and obstetrics (FIGO) initiative on pre-eclampsia: a pragmatic guide for first-trimester screening and prevention. Int J Gynaecol Obstet 145(Suppl 1):1–33. https://doi.org/10.1002/ijgo.12802 - DOI - PubMed - PMC
-
- Magee LA, Nicolaides KH, von Dadelszen P (2022) Preeclampsia. N Engl J Med 386(19):1817–32. https://doi.org/10.1056/NEJMra2109523 - DOI - PubMed
-
- Chappell LC, Cluver CA, Kingdom J, Tong S (2021) Pre-eclampsia. Lancet 398(10297):341–54. https://doi.org/10.1016/s0140-6736(20)32335-7 - DOI - PubMed
-
- Scott G, Gillon TE, Pels A, von Dadelszen P, Magee LA (2022) Guidelines-similarities and dissimilarities: a systematic review of international clinical practice guidelines for pregnancy hypertension. Am J Obstet Gynecol 226(2s):S1222-s36. https://doi.org/10.1016/j.ajog.2020.08.018 - DOI - PubMed
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous