妊娠晚期硫嘌呤代谢物分流会增加患有炎症性肠病的妇女发生妊娠期肝内胆汁淤积症的风险,可通过分次给药来控制。

Ralley Prentice, Emma Flanagan, Emily Wright, Lani Prideaux, William Connell, Miles Sparrow, Peter De Cruz, Mark Lust, Winita Hardikar, Rimma Goldberg, Sara Vogrin, Kirsten Palmer, Alyson Ross, Megan Burns, Tessa Greeve, Sally Bell
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引用次数: 0

摘要

背景和目的:暴露于硫嘌呤的孕妇发生妊娠期肝内胆汁淤积症(ICP)的风险增加。硫嘌呤 "分流"(6-甲氧巯基嘌呤(MMP)与 6-硫鸟嘌呤(TGN)之比大于 11)会在妊娠期进展,并可能促进 ICP 的发展。我们旨在探讨硫嘌呤暴露与ICP之间的关联,包括硫嘌呤分流的假设影响,并确定风险最小化策略:这项前瞻性多中心队列研究比较了暴露于硫嘌呤和生物单药治疗的孕妇。研究人员在孕前、每个孕期、分娩时和产后采集了疾病活动和产科结果数据、硫嘌呤代谢物、胆汁酸和转氨酶。硫嘌呤剂量管理由主治医生决定:结果:共纳入了 131 例暴露于硫嘌呤和 147 例暴露于单一生物疗法的孕妇。MMP/TGN比值从怀孕前三个月到怀孕后三个月一直在上升(p结论:硫嘌呤暴露与妊娠期糖尿病相关:硫嘌呤暴露与ICP风险增加有关,尤其是在产前剂量增加和妊娠晚期分流的情况下。后者可通过分次给药得到有效控制,但仍需进一步研究。
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Thiopurine Metabolite Shunting in Late Pregnancy Increases the Risk of Intrahepatic Cholestasis of Pregnancy in Women With Inflammatory Bowel Disease, and Can be Managed With Split Dosing.

Background and aims: The risk of intrahepatic cholestasis of pregnancy [ICP] is increased in thiopurine-exposed pregnancies. Thiopurine 'shunting', with a 6-methylmercaptopurine [MMP] to 6-thioguanine [TGN] ratio of >11, progresses over pregnancy, and may promote ICP development. We aimed to explore the association between thiopurine exposure and ICP, including the hypothesised impact of thiopurine shunting, and identify risk minimisation strategies.

Methods: This prospective multicentre cohort study compared thiopurine and biologic monotherapy-exposed pregnant participants. Disease activity and obstetric outcome data, thiopurine metabolites, bile acids, and transaminases were obtained before conception, in each trimester, at delivery, and postpartum. Thiopurine dose management was at the discretion of the treating physician.

Results: Included were 131 thiopurine and 147 biologic monotherapy-exposed pregnancies. MMP/TGN ratio increased from preconception to third trimester [p <0.01], with approximately 25% of participants shunting in pregnancy. Second trimester split dosing led to a decrease in the median MMP/TGN ratio from 18 (interquartile range [IQR] 6-57) to 3 [IQR 2-3.5] at delivery [p = 0.04]. The risk of ICP was increased in thiopurine-exposed pregnancies (6.7% [7/105] vs 0% [0/112], p <0.001), with all ICP cases occurring in the setting of antenatal thiopurine shunting. Thiopurine dose increases (risk ratio [RR] 8.10, 95% confidence interval [CI] 1.88-34.85, p = 0.005) and shunting in third trimester [6.20, 1.21-30.73, p = 0.028] and at delivery [14.18, 1.62-123.9, p = 0.016] were associated with an increased risk of ICP.

Conclusions: Thiopurine exposure is associated with an increased risk of ICP, particularly following dose increases antenatally and with shunting in late pregnancy. The latter may be effectively managed with split dosing, although further studies are warranted.

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