From the Department of Neurology (K.H., S.T., S.H., A.I.C., R.G.), St. Josef-Hospital-Katholisches Klinikum Bochum, Ruhr University Bochum; Department of Medical Informatics (M.T., N.T.), Biometry and Epidemiology, Ruhr University Bochum, Germany; Department of Neurology (A.M.L.-G.), Los Angeles Medical Center, Southern California Permanente Medical Group.
Neurol Neuroimmunol Neuroinflamm. 2023 May 22;10(4). doi: 10.1212/NXI.0000000000200110. Print 2023 Jul.
Discontinuation of fingolimod ≥2 months before pregnancy is recommended to minimize potential teratogenicity. The magnitude of MS pregnancy relapse risk, particularly severe relapses, after fingolimod cessation is unclear, as is whether this risk is reduced by pregnancy or modifiable factors.
Pregnancies who stopped fingolimod treatment within 1 year before or during pregnancy were identified from the German MS and Pregnancy Registry. Data were collected through structured telephone-administered questionnaires and neurologists' notes. Severe relapses were defined as a ≥2.0 increase in Expanded Disability Status Scale (EDSS) or new or worsening relapse-related ambulatory impairment. Women who continued to meet this definition 1 year postpartum were classified as reaching the Severe Relapse Disability Composite Score (SRDCS). Multivariable models accounting for measures of disease severity and repeated events were used.
Of the 213 pregnancies among 201 women (mean age at pregnancy onset 32 years) identified, 56.81% (n = 121) discontinued fingolimod after conception. Relapses during pregnancy (31.46%) and the postpartum year (44.60%) were common. Nine pregnancies had a severe relapse during pregnancy and additional 3 during the postpartum year. One year postpartum, 11 of these (6.32% of n = 174 with complete EDSS information) reached the SRDCS. Adjusted relapse rates during pregnancy were slightly higher compared with the year before pregnancy (relapse rate ratio = 1.24, 95% CI 0.91-1.68). Neither exclusive breastfeeding nor resuming fingolimod within 4 weeks of delivery were associated with a reduced risk of postpartum relapses. Most pregnancies relapsed during the first 3 months postpartum (n = 55/204, 26.96%).
Relapses during pregnancy after fingolimod cessation are common. Approximately 6% of women will retain clinically meaningful disability from these pregnancy-related, fingolimod cessation relapses 1 year postpartum. This information should be shared with women on fingolimod desiring pregnancy, and optimizing MS treatment with nonteratogenic approaches should be discussed.
为了将潜在的致畸风险降到最低,建议在怀孕前至少停药 2 个月。但目前尚不清楚在停用 fingolimod 后多发性硬化症(MS)怀孕复发的风险有多大,尤其是严重复发的风险,也不清楚这种风险是否可以通过怀孕或可改变的因素来降低。
从德国多发性硬化症与妊娠登记处确定了在妊娠前 1 年内或妊娠期间停用 fingolimod 的妊娠病例。通过结构化电话问卷调查和神经科医生的记录收集数据。严重复发定义为扩展残疾状况量表(EDSS)评分增加≥2.0 或新发或加重与复发相关的活动能力受损。在产后 1 年内仍符合该定义的女性被归类为达到严重复发残疾复合评分(SRDCS)。使用考虑疾病严重程度和重复事件的多变量模型。
在 201 名女性的 213 例妊娠中(妊娠起始时的平均年龄为 32 岁),56.81%(n=121)在受孕后停用 fingolimod。怀孕期间(31.46%)和产后(44.60%)复发很常见。9 例妊娠期间发生严重复发,另外 3 例发生在产后。产后 1 年,其中 11 例(n=174 例完全有 EDSS 信息者中的 6.32%)达到 SRDCS。与妊娠前相比,妊娠期间的调整复发率略高(复发率比值=1.24,95%CI 0.91-1.68)。产后 4 周内进行纯母乳喂养或恢复 fingolimod 治疗与降低产后复发风险无关。大多数妊娠在产后前 3 个月内复发(n=55/204,26.96%)。
停用 fingolimod 后怀孕时的复发很常见。大约 6%的女性在产后 1 年仍会因这些与怀孕相关的 fingolimod 停药复发而保留有临床意义的残疾。应该与想要怀孕的 fingolimod 女性分享这些信息,并应讨论优化无致畸作用的 MS 治疗方法。