Evidence map›Paper›PMID 40133418›Full record

ArticleScientific reports2025

Machine learning prediction of preterm birth in women under 35 using routine biomarkers in a retrospective cohort study.

Xiaojing Teng, Mengting Liu, Zhiyi Wang, Xueyan Dong

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Xiaojing TengDepartment of Laboratory Medicine, Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University, Hangzhou, Zhejiang, China.
Mengting LiuThe Fourth School of Clinical Medicine, Zhejiang Chinese Medical University (Hangzhou First People's Hospital), Hangzhou, China.
Zhiyi Wang *Department of Clinical Laboratory, Hangzhou Women's Hospital (Hangzhou Maternity and Child Health Care Hospital), Hangzhou, Zhejiang, China. kirawzy@hotmail.com.
Xueyan Dong *Department of Laboratory Medicine, Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University, Hangzhou, Zhejiang, China. dongxueyan82@163.com.

Funding

Zhejiang Medicine and Health Scientific Research 2022RC226
6 · The paper itself

Abstract

Preterm birth (PTB), defined as delivery before 37 weeks, affects 15 million infants annually, accounting for 11% of live births and over 35% of neonatal deaths. While advanced maternal age (≥ 35 years) is a known risk factor, PTB risk in women under 35 is underexplored. This study aimed to develop a machine learning-based model for PTB prediction in women under 35. A retrospective cohort of 2606 cases (2019-2022) equally split between full-term and preterm births was analyzed. Logistic Regression, LightGBM, Gradient Boosting Decision Tree (GBDT), and XGBoost models were evaluated. External validation was conducted using 803 independent cases (2023). Model performance was assessed using area under the curve (AUC), accuracy, sensitivity, and specificity. SHAP (SHapley Additive exPlanations) values were used to interpret model predictions. The XGBoost model demonstrated superior performance with an AUC of 0.893 (95% CI: 0.860-0.925) on the validation set. In comparison, Logistic Regression, LightGBM, and GBDT achieved AUCs of 0.872, 0.840, and 0.879, respectively. External validation of the XGBoost model yielded an AUC of 0.91 (95% CI: 0.889-0.931). SHAP analysis highlighted seven key predictors: alkaline phosphatase (ALP), alpha-fetoprotein (AFP), hemoglobin (HGB), urea (UREA), lymphocyte count (Lym1), sodium (Na), and red cell distribution width coefficient of variation (RDWCV). The XGBoost model provides accurate PTB risk prediction and key insights for early intervention in women under 35, supporting its potential clinical utility.

Indexed as

BiomarkersMachine LearningPremature BirthAdultFemaleHumansInfant, NewbornLogistic ModelsPregnancyRetrospective StudiesRisk FactorsBiomarkersMachine learningPreterm birth risk predictionSHAP value analysisWomen under 35XGBoost

Identifiers

PMID40133418
PMCPMC11937320

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.