血清IGF-1、IGFBP-3水平对妊娠期糖尿病初产妇不良妊娠结局的评估价值
作者: |
1张雪冰,
1李荣,
1何辉
1 池州市人民医院妇产科,安徽 池州 247000 |
通讯: |
张雪冰
Email: 875431776@qq.com |
DOI: | 10.3978/j.issn.2095-6959.2023.221285 |
摘要
目的:探讨血清胰岛素样生长因子1(insulin-like growth factor-1,IGF-1)、胰岛素样生长因子结合蛋白3(insulin-like growth factor-binding protein-3,IGFBP-3)对妊娠期糖尿病(gestational diabetes mellitus,GDM)初产妇不良妊娠结局的评估价值。方法:选取GDM初产妇160例(GDM组)与健康孕产妇54例(对照组),均于孕晚期检测血清IGF-1、IGFBP-3水平,对比2组IGF-1、IGFBP-3水平差异;分析IGF-1、IGFBP-3水平与GDM血糖控制状况(分为控制不良组与控制良好组)及妊娠结局(分为不良妊娠结局组与良好妊娠结局组)的关系,并应用受试者操作特征(receiver operating characteristic,ROC)曲线评价IGF-1、IGFBP-3及其联合对不良妊娠结局的预测效能。结果:相比对照组,GDM组孕晚期血清IGF-1水平显著降低(P<0.05),IGFBP-3水平显著增高(P<0.05)。相比控制良好组,控制不良组IGF-1水平显著降低(P<0.05),IGFBP-3水平显著增高(P<0.05)。相比良好妊娠结局组,不良妊娠结局组糖化血红蛋白(glycosylated hemoglobin,HbA1c)、IGFBP-3水平均显著增高(均P<0.05),IGF-1水平显著降低(P<0.05)。Logistic回归分析显示:血清IGF-1、IGFBP-3是GDM初产妇出现不良妊娠结局的独立影响因素(均P<0.05)。ROC曲线分析显示:IGF-1预测GDM不良妊娠结局的曲线下面积(area under the curve,AUC)为0.732(95% CI:0.656~0.799),IGFBP-3的AUC为0.648(95% CI:0.568~0.722),二者差异无统计学意义(Z=1.251,P=0.165);二者联合的AUC为0.771(95% CI:0.698~0.833),优于单独使用IGF-1、IGFBP-3(Z=2.314、2.725,P=0.013、0.006)。结论:血清IGF-1、IGFBP-3与GDM初产妇不良妊娠结局有关,二者联合检测可提高对不良妊娠结局的预测价值。
关键词:
妊娠期糖尿病;妊娠结局;胰岛素样生长因子1;胰岛素样生长因子结合蛋白3
Evaluation value of serum IGF-1 and IGFBP-3 levels on adverse pregnancy outcomes in primipara with gestational diabetes mellitus
CorrespondingAuthor: ZHANG Xuebing Email: 875431776@qq.com
DOI: 10.3978/j.issn.2095-6959.2023.221285
Abstract
Objective: To investigate the predictive value of serum insulin-like growth factor-1 (IGF-1) and insulin-like growth factor-binding protein-3 (IGFBP-3) on adverse pregnancy outcomes of primipara with gestational diabetes mellitus (GDM).
Methods: A total of 160 primiparous women with GDM (GDM group) and 54 healthy pregnant women (control group) were selected. The serum levels of IGF-1 and IGFBP-3 were measured at late pregnancy and compared between the 2 groups. The relationship between the levels of IGF-1 and IGFBP-3, blood glucose control (divided into a group with good blood glucose control and a group with poor blood glucose control) and pregnancy outcomes (divided into a good pregnancy outcome group and a adverse pregnancy outcome group) in GDM was analyzed. The receiver operating characteristic (ROC) curve was used to evaluate the predictive effect of IGF-1, IGFBP-3, and their combination on adverse pregnancy outcomes.
Results: Compared with the control group, the serum IGF-1 level in the GDM group at late pregnancy was significantly decreased (P<0.05), and the IGFBP-3 level was significantly increased (P<0.05). Compared with the group with good blood glucose control, the IGF-1 level in the group with poor blood glucose control was significantly decreased (P<0.05), and the IGFBP-3 level was significantly increased (P<0.05). Compared with the good pregnancy outcome group, the levels of glycosylated hemoglobin (HbA1c) and IGFBP-3 in the adverse pregnancy outcome group were significantly increased (both P<0.05) and the level of IGF-1 was significantly decreased (P<0.05). Logistic regression analysis showed that serum IGF-1 and IGFBP-3 were independent factors affecting adverse pregnancy outcomes in GDM primiparas (both P<0.05). ROC curve analysis showed that the area under the curve (AUC) of IGF-1 in predicting adverse pregnancy outcomes of GDM was 0.732 (95% CI 0.656 to 0.799), and the AUC of IGFBP-3 was 0.648 (95% CI 0.568 to 0.722). There was no significant difference between the 2 groups (Z=1.251, P=0.165). The AUC of the combination was 0.771 (95% CI 0.698 to 0.833), which was better than that of single IGF-1 or IGFBP-3 (Z=2.314, 2.725; P=0.013, 0.006).
Conclusion: Serum levels of IGF-1 and IGFBP-3 are associated with adverse pregnancy outcomes in GDM primipara, and the combined detection of them can improve the predictive value of adverse pregnancy outcomes.
Keywords:
gestational diabetes mellitus; pregnancy outcome; insulin-like growth factor-1; insulin-like growth factor-binding protein-3
Methods: A total of 160 primiparous women with GDM (GDM group) and 54 healthy pregnant women (control group) were selected. The serum levels of IGF-1 and IGFBP-3 were measured at late pregnancy and compared between the 2 groups. The relationship between the levels of IGF-1 and IGFBP-3, blood glucose control (divided into a group with good blood glucose control and a group with poor blood glucose control) and pregnancy outcomes (divided into a good pregnancy outcome group and a adverse pregnancy outcome group) in GDM was analyzed. The receiver operating characteristic (ROC) curve was used to evaluate the predictive effect of IGF-1, IGFBP-3, and their combination on adverse pregnancy outcomes.
Results: Compared with the control group, the serum IGF-1 level in the GDM group at late pregnancy was significantly decreased (P<0.05), and the IGFBP-3 level was significantly increased (P<0.05). Compared with the group with good blood glucose control, the IGF-1 level in the group with poor blood glucose control was significantly decreased (P<0.05), and the IGFBP-3 level was significantly increased (P<0.05). Compared with the good pregnancy outcome group, the levels of glycosylated hemoglobin (HbA1c) and IGFBP-3 in the adverse pregnancy outcome group were significantly increased (both P<0.05) and the level of IGF-1 was significantly decreased (P<0.05). Logistic regression analysis showed that serum IGF-1 and IGFBP-3 were independent factors affecting adverse pregnancy outcomes in GDM primiparas (both P<0.05). ROC curve analysis showed that the area under the curve (AUC) of IGF-1 in predicting adverse pregnancy outcomes of GDM was 0.732 (95% CI 0.656 to 0.799), and the AUC of IGFBP-3 was 0.648 (95% CI 0.568 to 0.722). There was no significant difference between the 2 groups (Z=1.251, P=0.165). The AUC of the combination was 0.771 (95% CI 0.698 to 0.833), which was better than that of single IGF-1 or IGFBP-3 (Z=2.314, 2.725; P=0.013, 0.006).
Conclusion: Serum levels of IGF-1 and IGFBP-3 are associated with adverse pregnancy outcomes in GDM primipara, and the combined detection of them can improve the predictive value of adverse pregnancy outcomes.