Alroughani Raed, Altintas Ayse, Al Jumah Mohammed, Sahraian Mohammadali, Alsharoqi Issa, AlTahan Abdurahman, Daif Abdulkader, Dahdaleh Maurice, Deleu Dirk, Fernandez Oscar, Grigoriadis Nikolaos, Inshasi Jihad, Karabudak Rana, Taha Karim, Totolyan Natalia, Yamout Bassem I, Zakaria Magd, Bohlega Saeed
Division of Neurology, Amiri Hospital and Division of Neurology, Dasman Diabetes Institute, Dasman, Kuwait.
Division of Neurology, Cerrahpasa School of Medicine, Istanbul University, Istanbul, Turkey.
Mult Scler Int. 2016;2016:1034912. doi: 10.1155/2016/1034912. Epub 2016 Dec 18.
The burden of multiple sclerosis (MS) in women of childbearing potential is increasing, with peak incidence around the age of 30 years, increasing incidence and prevalence, and growing female : male ratio. Guidelines recommend early use of disease-modifying therapies (DMTs), which are contraindicated or recommended with considerable caution, during pregnancy/breastfeeding. Many physicians are reluctant to prescribe them for a woman who is/is planning to be pregnant. Interferons are not absolutely contraindicated during pregnancy, since interferon- appears to lack serious adverse effects in pregnancy, despite a warning in its labelling concerning risk of spontaneous abortion. Glatiramer acetate, natalizumab, and alemtuzumab also may not induce adverse pregnancy outcomes, although natalizumab may induce haematologic abnormalities in newborns. An accelerated elimination procedure is needed for teriflunomide if pregnancy occurs on treatment or if pregnancy is planned. Current evidence supports the contraindication for fingolimod during pregnancy; data on other DMTs remains limited. Increased relapse rates following withdrawal of some DMTs in pregnancy are concerning and require further research. The postpartum period brings increased risk of disease reactivation that needs to be carefully addressed through effective communication between treating physicians and mothers intending to breastfeed. We address the potential for use of the first- and second-line DMTs in pregnancy and lactation.
育龄期女性多发性硬化症(MS)的负担正在增加,发病高峰年龄约为30岁,发病率和患病率不断上升,且女性与男性的比例也在增加。指南建议在怀孕/哺乳期间尽早使用疾病修正疗法(DMTs),但这些疗法在孕期/哺乳期为禁忌或需谨慎使用。许多医生不愿为已怀孕或计划怀孕的女性开这些药物。干扰素在孕期并非绝对禁忌,因为尽管其标签中有关于自然流产风险的警告,但干扰素在孕期似乎没有严重不良反应。醋酸格拉替雷、那他珠单抗和阿仑单抗也可能不会导致不良妊娠结局,不过那他珠单抗可能会导致新生儿血液学异常。如果在治疗期间怀孕或计划怀孕,对于特立氟胺需要采取加速消除程序。目前的证据支持芬戈莫德在孕期禁忌使用;关于其他DMTs的数据仍然有限。在孕期停用某些DMTs后复发率增加令人担忧,需要进一步研究。产后疾病重新激活的风险增加,需要通过治疗医生与打算母乳喂养的母亲之间的有效沟通来谨慎应对。我们探讨了一线和二线DMTs在怀孕和哺乳期间的使用可能性。