Prediction of gestational diabetes mellitus by multiple biomarkers at early gestation

被引:0
|
作者
Yang, Meng-Nan [1 ,2 ]
Zhang, Lin [3 ]
Wang, Wen-Juan [1 ,4 ]
Huang, Rong [2 ]
He, Hua [1 ]
Zheng, Tao [5 ]
Zhang, Guang-Hui [6 ]
Fang, Fang [1 ]
Cheng, Justin [2 ]
Li, Fei [1 ]
Ouyang, Fengxiu [1 ]
Li, Jiong [1 ,7 ]
Zhang, Jun [1 ]
Luo, Zhong-Cheng [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Xinhua Hosp, Early Life Hlth Inst, Minist Educ,Shanghai Key Lab Childrens Environm Hl, KongJiang Rd, Shanghai 200092, Peoples R China
[2] Univ Toronto, Lunenfeld Tanenbaum Res Inst, Fac Med, Prosserman Ctr Populat Hlth Res,Dept Obstet & Gyne, L5-240,Murray St 60, Toronto, ON M5T 3H7, Canada
[3] Shanghai Jiao Tong Univ, Int Peace Matern & Child Hlth Hosp, Obstet & Gynecol, Sch Med, Shanghai 200030, Peoples R China
[4] Shandong First Med Univ, Shandong Acad Med Sci, Clin Skills Ctr, Sch Clin Med, Jinan, Peoples R China
[5] Shanghai Jiao Tong Univ, Xinhua Hosp, Obstet & Gynecol, Sch Med, Shanghai 200092, Peoples R China
[6] Shanghai Jiao Tong Univ, Xinhua Hosp, Dept Clin Assay Lab, Sch Med, Shanghai 200092, Peoples R China
[7] Nanjing Med Univ, Sch Publ Hlth, Dept Epidemiol, State Key Lab Reprod Med, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
Gestational diabetes; Fasting plasma glucose; IGFBP-2; Predictive biomarker; Early gestation; FASTING PLASMA-GLUCOSE; 1ST TRIMESTER; BINDING PROTEIN-2; INSULIN; PREGNANCY; RISK; GROWTH; CHILDHOOD; OBESITY; CLASSIFICATION;
D O I
10.1186/s12884-024-06651-4
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BackgroundIt remains unclear which early gestational biomarkers can be used in predicting later development of gestational diabetes mellitus (GDM). We sought to identify the optimal combination of early gestational biomarkers in predicting GDM in machine learning (ML) models.MethodsThis was a nested case-control study including 100 pairs of GDM and euglycemic (control) pregnancies in the Early Life Plan cohort in Shanghai, China. High sensitivity C reactive protein, sex hormone binding globulin, insulin-like growth factor I, IGF binding protein 2 (IGFBP-2), total and high molecular weight adiponectin and glycosylated fibronectin concentrations were measured in serum samples at 11-14 weeks of gestation. Routine first-trimester blood test biomarkers included fasting plasma glucose (FPG), serum lipids and thyroid hormones. Five ML models [stepwise logistic regression, least absolute shrinkage and selection operator (LASSO), random forest, support vector machine and k-nearest neighbor] were employed to predict GDM. The study subjects were randomly split into two sets for model development (training set, n = 70 GDM/control pairs) and validation (testing set: n = 30 GDM/control pairs). Model performance was evaluated by the area under the curve (AUC) in receiver operating characteristics.ResultsFPG and IGFBP-2 were consistently selected as predictors of GDM in all ML models. The random forest model including FPG and IGFBP-2 performed the best (AUC 0.80, accuracy 0.72, sensitivity 0.87, specificity 0.57). Adding more predictors did not improve the discriminant power.ConclusionThe combination of FPG and IGFBP-2 at early gestation (11-14 weeks) could predict later development of GDM with moderate discriminant power. Further validation studies are warranted to assess the utility of this simple combination model in other independent cohorts. It remains unclear which early gestational biomarkers can be used in predicting later development of gestational diabetes mellitus.The present study demonstrates that the combination of fasting plasma glucose and insulin-like growth factor binding protein 2 at early gestation can predict later development of gestational diabetes with moderate discriminant power.
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页数:9
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