Department of Women and Children's Health, King's College London, London, UK.
Department of Obstetrics and Gynaecology, University College London Hospitals NHS Foundation Trust, London, UK.
Lancet Gastroenterol Hepatol. 2021 Jul;6(7):547-558. doi: 10.1016/S2468-1253(21)00074-1. Epub 2021 Apr 27.
Ursodeoxycholic acid is commonly used to treat intrahepatic cholestasis of pregnancy, yet its largest trial detected minimal benefit for a composite outcome (stillbirth, preterm birth, and neonatal unit admission). We aimed to examine whether ursodeoxycholic acid affects specific adverse perinatal outcomes.
In this systematic review and individual participant data meta-analysis, we searched PubMed, Web of Science, Embase, MEDLINE, CINAHL, Global Health, MIDIRS, and Cochrane without language restrictions for relevant articles published between database inception, and Jan 1, 2020, using search terms referencing intrahepatic cholestasis of pregnancy, ursodeoxycholic acid, and perinatal outcomes. Eligible studies had 30 or more study participants and reported on at least one individual with intrahepatic cholestasis of pregnancy and bile acid concentrations of 40 μmol/L or more. We also included two unpublished cohort studies. Individual participant data were collected from the authors of selected studies. The primary outcome was the prevalence of stillbirth, for which we anticipated there would be insufficient data to achieve statistical power. Therefore, we included a composite of stillbirth and preterm birth as a main secondary outcome. A mixed-effects meta-analysis was done using multi-level modelling and adjusting for bile acid concentration, parity, and multifetal pregnancy. Individual participant data analyses were done for all studies and in different subgroups, which were produced by limiting analyses to randomised controlled trials only, singleton pregnancies only, or two-arm studies only. This study is registered with PROSPERO, CRD42019131495.
The authors of the 85 studies fulfilling our inclusion criteria were contacted. Individual participant data from 6974 women in 34 studies were included in the meta-analysis, of whom 4726 (67·8%) took ursodeoxycholic acid. Stillbirth occurred in 35 (0·7%) of 5097 fetuses among women with intrahepatic cholestasis of pregnancy treated with ursodeoxycholic acid and in 12 (0·6%) of 2038 fetuses among women with intrahepatic cholestasis of pregnancy not treated with ursodeoxycholic acid (adjusted odds ratio [aOR] 1·04, 95% CI 0·35-3·07; p=0·95). Ursodeoxycholic acid treatment also had no effect on the prevalence of stillbirth when considering only randomised controlled trials (aOR 0·29, 95% CI 0·04-2·42; p=0·25). Ursodeoxycholic acid treatment had no effect on the prevalence of the composite outcome in all studies (aOR 1·28, 95% CI 0·86-1·91; p=0·22), but was associated with a reduced composite outcome when considering only randomised controlled trials (0·60, 0·39-0·91; p=0·016).
Ursodeoxycholic acid treatment had no significant effect on the prevalence of stillbirth in women with intrahepatic cholestasis of pregnancy, but our analysis was probably limited by the low overall event rate. However, when considering only randomised controlled trials, ursodeoxycholic acid was associated with a reduction in stillbirth in combination with preterm birth, providing evidence for the clinical benefit of antenatal ursodeoxycholic acid treatment.
Tommy's, the Wellcome Trust, ICP Support, and the National Institute for Health Research.
熊去氧胆酸常用于治疗妊娠肝内胆汁淤积症,但它最大的试验检测到复合结局(死产、早产和新生儿病房入院)的益处最小。我们旨在研究熊去氧胆酸是否会影响特定的围产期不良结局。
在这项系统评价和个体参与者数据荟萃分析中,我们检索了 PubMed、Web of Science、Embase、MEDLINE、CINAHL、Global Health、MIDIRS 和 Cochrane,检索时间从数据库建立开始到 2020 年 1 月 1 日,使用的检索词包括妊娠肝内胆汁淤积症、熊去氧胆酸和围产期结局。符合条件的研究有 30 名或以上的研究参与者,并且至少有 1 名患有肝内胆汁淤积症且胆汁酸浓度为 40μmol/L 或以上的个体参与者。我们还纳入了两项未发表的队列研究。从选定研究的作者处收集了个体参与者数据。主要结局为死产的发生率,我们预计没有足够的数据来达到统计学功效。因此,我们纳入了死产和早产的复合结局作为主要次要结局。使用多水平模型进行混合效应荟萃分析,并调整了胆汁酸浓度、产次和多胎妊娠。对所有研究和不同亚组进行了个体参与者数据分析,这些亚组的分析仅限于随机对照试验、单胎妊娠或双臂研究。这项研究在 PROSPERO 注册,注册号为 CRD42019131495。
我们联系了符合纳入标准的 85 项研究的作者。共有 34 项研究的 6974 名女性的个体参与者数据纳入了荟萃分析,其中 4726 名(67.8%)服用了熊去氧胆酸。在接受熊去氧胆酸治疗的妊娠肝内胆汁淤积症女性中,死产发生在 5097 名胎儿中的 35 名(0.7%),在未接受熊去氧胆酸治疗的妊娠肝内胆汁淤积症女性中,死产发生在 2038 名胎儿中的 12 名(0.6%)(调整后的优势比[aOR]1.04,95%CI0.35-3.07;p=0.95)。当仅考虑随机对照试验时,熊去氧胆酸治疗对死产的发生率也没有影响(aOR0.29,95%CI0.04-2.42;p=0.25)。在所有研究中,熊去氧胆酸治疗对复合结局的发生率均无影响(aOR1.28,95%CI0.86-1.91;p=0.22),但当仅考虑随机对照试验时,熊去氧胆酸治疗与复合结局降低相关(0.60,0.39-0.91;p=0.016)。
熊去氧胆酸治疗对妊娠肝内胆汁淤积症女性的死产发生率没有显著影响,但我们的分析可能受到总体事件发生率低的限制。然而,当仅考虑随机对照试验时,熊去氧胆酸与死产和早产的复合结局减少相关,为产前熊去氧胆酸治疗的临床益处提供了证据。
汤米基金会、威康信托、ICP 支持和英国国家健康研究所。