Saito Satoshi, Ikeguchi Ryotaro, Kitagawa Kazuo, Shimizu Yuko
Department of Neurology Tokyo Women's Medical University School of Medicine, 8-1, Kawadacho, Shinjukuku, Tokyo, Japan.
Case Rep Neurol Med. 2024 Jul 16;2024:7808140. doi: 10.1155/2024/7808140. eCollection 2024.
Interferon and glatiramer acetate are the disease-modifying drugs (DMDs) considered relatively safe for use in pregnant women with multiple sclerosis (MS); however, the safety profile of dimethyl fumarate (DMF) and natalizumab (NTZ) in this population remains inconclusive. Here, we present four cases of pregnant women with MS who were treated with DMF and NTZ ( = 2 patients, each) during their pregnancy and discuss our observations with the use of these drugs and the clinical courses of the patients. We retrospectively examined relapse of MS during pregnancy and after delivery; duration of exposure to DMDs; maternal, fetal, and neonatal adverse events; breastfeeding; and timing of resumption of DMDs. The two patients treated with DMF discontinued treatment 5 or 6 weeks after the discovery of pregnancy. DMF was resumed 1 week postpartum, and mixed breastfeeding was initiated. Brain magnetic resonance imaging in one patient 9 months after delivery revealed a new lesion; however, it was not classified as a clinical relapse. In two patients treated with NTZ, the dosing interval was extended to 6 weeks after the discovery of pregnancy. One patient discontinued NTZ at 30 weeks and the other at 25 weeks of gestation, as a slight restriction in fetal growth was observed owing to hyperemesis gravidarum. Both patients opted for formula feeding, and no relapse was observed within 1 year postpartum. Additionally, no abnormalities were observed in any of the patients during the perinatal period, and their development was normal. Investigation of drug safety in pregnant and parturient women primarily relies on registries, postmarketing surveillance, and case reports due to ethical limitations on conducting randomized controlled trials. Our findings demonstrated that DMF and NTZ were not contraindicated during pregnancy or the perinatal period in women with MS; nevertheless, vigilant monitoring is essential to ensure the safety of these drugs.
干扰素和醋酸格拉替雷是被认为对患有多发性硬化症(MS)的孕妇使用相对安全的疾病修正药物(DMDs);然而,富马酸二甲酯(DMF)和那他珠单抗(NTZ)在该人群中的安全性仍然尚无定论。在此,我们介绍4例患有MS的孕妇,她们在孕期接受了DMF和NTZ治疗(各2例),并讨论我们对这些药物使用情况及患者临床病程的观察结果。我们回顾性研究了孕期及产后MS的复发情况;DMDs的暴露持续时间;母体、胎儿和新生儿不良事件;母乳喂养情况;以及恢复使用DMDs的时间。2例接受DMF治疗的患者在发现怀孕后5或6周停止治疗。产后1周恢复使用DMF,并开始混合喂养。1例患者在产后9个月的脑部磁共振成像显示有新病灶;然而,该病灶未被归类为临床复发。2例接受NTZ治疗的患者,在发现怀孕后给药间隔延长至6周。1例患者在妊娠30周时停用NTZ,另1例在妊娠25周时停用,因为观察到由于妊娠剧吐胎儿生长略有受限。2例患者均选择配方奶喂养,产后1年内未观察到复发。此外,围产期所有患者均未观察到异常,其发育正常。由于进行随机对照试验存在伦理限制,对孕妇和产妇药物安全性的研究主要依赖于登记处、上市后监测和病例报告。我们的研究结果表明,DMF和NTZ在患有MS的女性孕期或围产期并非禁忌;然而,进行 vigilant监测对于确保这些药物的安全性至关重要。