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预防医学  2025, Vol. 37 Issue (7): 727-731    DOI: 10.19485/j.cnki.issn2096-5087.2025.07.018
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妊娠期肝内胆汁淤积症患者胆汁酸谱分析
胡瑜洁, 施新颜, 沈涌海, 周雅媛, 陈宇
杭州市妇产科医院,浙江 杭州 310008
Analysis of bile acid profile among patients with intrahepatic cholestasis of pregnancy
HU Yujie, SHI Xinyan, SHEN Yonghai, ZHOU Yayuan, CHEN Yu
Hangzhou Obstetrics and Gynecology Hospital, Hangzhou, Zhejiang 310008, China
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摘要 目的 分析妊娠期肝内胆汁淤积症(ICP)患者不同妊娠期胆汁酸谱差异,为孕妇早期防治ICP,优化母婴健康结局提供参考。方法 选择2021—2023年在杭州市妇产科医院进行常规产检并分娩的孕妇为研究对象,根据妊娠期肝内胆汁淤积症指南(2020版),分为正常组、轻度ICP组和中/重度ICP组。通过医院产科电子病历系统收集年龄、产次和孕次等基本信息,通过医院实验室信息系统收集肝功能指标和7种胆汁酸谱亚型;比较不同妊娠期3组孕妇7种胆汁酸谱亚型差异。结果 纳入孕妇238人,其中正常组57人,占23.95%;轻度ICP组136例,占57.14%;中/重度ICP组45例,占18.91%。3组孕妇总胆汁酸、胆酸(CA)、鹅脱氧胆酸(CDCA)、甘氨鹅脱氧胆酸(GCDCA)、甘氨胆酸(GCA)和牛磺胆酸(TCA)差异有统计学意义(均P<0.05);与正常组比较,轻度ICP组和中/重度ICP组CA、GCDCA、GCA和TCA较高;与轻度ICP组比较,中/重度ICP组GCA较高(均P<0.05)。妊娠早期、中期和晚期3组孕妇GCDCA、GCA和TCA差异有统计学意义(均P<0.05);与正常组比较,轻度ICP组妊娠早期、中期GCDCA和GCA较高,中/重度ICP组妊娠早期TCA和妊娠晚期GCDCA、GCA较高;与轻度ICP组比较,中/重度ICP组妊娠早期TCA和妊娠晚期GCA较高。结论 ICP患者GCDCA、GCA和TCA在不同妊娠期均高于正常孕妇,可根据胆汁酸谱变化特点制定个性化妊娠期管理方案,优化母婴健康结局。
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胡瑜洁
施新颜
沈涌海
周雅媛
陈宇
关键词 妊娠期肝内胆汁淤积症胆汁酸谱妊娠期管理    
AbstractObjective To analyze the differences in bile acid profiles during different pregnancy durations of patients with intrahepatic cholestasis of pregnancy (ICP), so as to provide a reference for early prevention and treatment of ICP and optimization of maternal-infant health outcomes. Methods Pregnant women who underwent routine prenatal examinations and delivered at Hangzhou Obstetrics and Gynecology Hospital from 2021 to 2023 were selected as study subjects. According to the ICP guidelines (2020), pregnant women were categorized into normal group, mild ICP group, and moderate/severe ICP group. Age, parity, and gravidity were collected through the obstetric electronic medical record system, liver function indicators and seven bile acid levels were collected through the hospital's laboratory information system. Differences in bile acid profiles across pregnancy durations among the three groups were compared. Results A total of 238 pregnant women were enrolled, including 57 cases (23.95%) in the normal group, 136 cases (57.14%) in the mild ICP group, and 45 cases (18.91%) in the moderate/severe ICP group. There were statistically significant differences between the three groups in total bile acid (TBA), cholic acid (CA), chenodeoxycholic acid (CDCA), glycochenodeoxycholic acid (GCDCA), glycocholic acid (GCA), taurocholic acid (TCA) levels (all P<0.05). Compared with the normal group, CA, GCDCA and GCA, and TCA were higher in the mild and moderate/severe ICP groups; compared with the mild ICP group, GCA was higher in the moderate/severe ICP group (all P<0.05). Significant differences were observed in the levels of GCDCA, GCA, and TCA among three groups pregnant women in the early, mid, and late pregnancy (all P<0.05). Compared with the normal group, mild ICP group had higher GCDCA and GCA in the early and mid pregnancy; moderate/severe ICP group had higher TCA in the early pregnancy and higher GCDCA and GCA in the late pregnancy. Compared with the mild ICP group, mild ICP group had higher TCA in the early pregnancy and the moderate/severe ICP group had higher GCA in the late pregnancy. Conclusions GCDCA, GCA, and TCA levels remain higher in ICP patients than in normal pregnant women across all pregnancy durations. Personalized perinatal management plans can be developed based on bile acid profile dynamics to optimize maternal-fetal outcomes.
Key wordsintrahepatic cholestasis of pregnancy    bile acid profile    pregnancy management
收稿日期: 2025-01-22      修回日期: 2025-06-29      出版日期: 2025-07-10
中图分类号:  R714.255  
基金资助:杭州市农业与社会发展科技计划引导项目(20211231Y070)
作者简介: 胡瑜洁,本科,检验师,主要从事产科妊娠期肝内胆汁淤积症与代谢及肠道微生态工作
通信作者: 陈宇,E-mail:64684154@qq.com   
引用本文:   
胡瑜洁, 施新颜, 沈涌海, 周雅媛, 陈宇. 妊娠期肝内胆汁淤积症患者胆汁酸谱分析[J]. 预防医学, 2025, 37(7): 727-731.
HU Yujie, SHI Xinyan, SHEN Yonghai, ZHOU Yayuan, CHEN Yu. Analysis of bile acid profile among patients with intrahepatic cholestasis of pregnancy. Preventive Medicine, 2025, 37(7): 727-731.
链接本文:  
http://www.zjyfyxzz.com/CN/10.19485/j.cnki.issn2096-5087.2025.07.018      或      http://www.zjyfyxzz.com/CN/Y2025/V37/I7/727
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