胎儿素B可能是预测肝内胆汁淤积症产妇和新生儿结局的潜在标志物:前瞻性病例对照研究

IF 1 Q4 OBSTETRICS & GYNECOLOGY
Jasmina Begum, Sweta Singh, Gautom Kumar Saharia, Manas Kumar Panigrahi
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引用次数: 0

摘要

目的:探讨健康孕妇和妊娠肝内胆汁淤积症(IHCP)妇女血清胎蛋白B水平及其与妊娠结局的关系。材料和方法:这是一项前瞻性病例对照研究,我们纳入了60名患有IHCP的单胎孕妇和60名健康匹配的妊娠晚期孕妇。分析这些患者的血清胎儿素B水平。所有患者都进行了前瞻性随访,直到分娩,并获得了与孕产妇、围产期和新生儿结局相关的数据。结果:IHCP组的总胆汁酸水平和肝功能测试明显高于对照组(结论:我们没有注意到IHCP组和对照组之间血清胎儿蛋白B水平的显著差异,也不能将其水平与除出生体重外的孕产妇和围产期不良结局联系起来,因此血清胎儿蛋白B不是用于揭示IHCP病理生理学的有效标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fetuin B may be a potential marker for predicting maternal and neonatal outcomes in intrahepatic cholestasis: Prospective case-control study.

Fetuin B may be a potential marker for predicting maternal and neonatal outcomes in intrahepatic cholestasis: Prospective case-control study.

Fetuin B may be a potential marker for predicting maternal and neonatal outcomes in intrahepatic cholestasis: Prospective case-control study.

Fetuin B may be a potential marker for predicting maternal and neonatal outcomes in intrahepatic cholestasis: Prospective case-control study.

Objective: To investigate the levels of serum fetuin B in healthy pregnant women and women with intrahepatic cholestasis of pregnancy (IHCP) and their association with pregnancy outcomes.

Materials and methods: This was a prospective case-control study, we included sixty singleton pregnant women with IHCP and sixty healthy-matched pregnant women in their third trimester. The serum fetuin B levels of these patients were analyzed. All the patients were followed up prospectively until delivery and data related to maternal, perinatal, and neonatal outcomes were obtained.

Results: Total bile acid levels and liver function tests were significantly higher in the IHCP group than in the control group (p<0.0001 and <0.0001, respectively). The serum fetuin B concentrations were higher in the IHCP group than in the control group, without any significant group difference (p=0.105). Preterm delivery, iatrogenic preterm delivery, and birth weight ≤2.500 gm are only significantly associated with serum fetuin B levels respectively (p<0.05). The diagnostic performance of serum bile acids [area under the curve (AUC)=0.998] was significantly better than that of fetuin B (AUC=0.586) (DeLong's test p≤0.001).

Conclusion: We neither noted a significant difference between the IHCP and control groups concerning the serum fetuin B levels nor could we correlate its levels with adverse maternal and perinatal outcomes except with birth weight, thereby serum fetuin B was not an effective marker for use in shedding light on the pathophysiology of IHCP.

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