Novartis Pharmaceuticals Corporation, One Health Plaza, Building 339-1131, East Hanover, NJ, 07936-1080, USA.
Novartis Pharma AG, Basel, Switzerland.
J Neurol. 2020 Sep;267(9):2721-2731. doi: 10.1007/s00415-020-09913-1. Epub 2020 May 22.
Neurologists managing women with Multiple Sclerosis (MS) need information about the safety of disease modifying drugs (DMDs) during pregnancy. However, this knowledge is limited. The present study aims to summarize previous studies by performing a systematic review and meta-analyses. The terms "multiple sclerosis" combined with DMDs of interest and a broad profile for pregnancy terms were used to search Embase and Medline databases to identify relevant studies published from January 2000 to July 2019.1260 studies were identified and ten studies met our inclusion criteria. Pooled risk ratios (RR) of pregnancy and birth outcomes in pregnancies exposed to DMDs compared to those not exposed were calculated using a random effects model. For spontaneous abortion RR = 1.14, 95% CI 0.99-1.32, for preterm births RR = 0.93, 95% CI 0.72-1.21 and for major congenital malformations RR = 0.86, 95% CI 0.47-1.56. The most common major congenital malformations reported in MS patients exposed to MS drugs were atrial septal defect (ASD) (N = 4), polydactyly (N = 4) and club foot (N = 3), which are among the most prevalent birth defects observed in the general population. In conclusion, interferons, glatiramer acetate or natalizumab, do not appear to increase the risk for spontaneous abortions, pre-term birth or major congenital malformations. There were very few patients included that were exposed to fingolimod, azathioprine and rituximab; therefore, these results cannot be generalized across drugs. Future studies including internal comparators are needed to enable treating physicians and their patients to decide on the best treatment options.
神经科医生在管理多发性硬化症(MS)女性患者时需要了解疾病修饰药物(DMD)在怀孕期间的安全性。然而,这方面的知识非常有限。本研究旨在通过系统评价和荟萃分析来总结之前的研究。使用“多发性硬化症”结合感兴趣的 DMD 药物和广泛的妊娠术语,在 Embase 和 Medline 数据库中进行检索,以确定从 2000 年 1 月至 2019 年 7 月发表的相关研究。共确定了 1260 项研究,其中 10 项研究符合我们的纳入标准。使用随机效应模型计算暴露于 DMD 药物的妊娠与出生结局的合并风险比(RR),与未暴露于 DMD 药物的妊娠相比。自然流产 RR=1.14,95%CI 0.99-1.32,早产 RR=0.93,95%CI 0.72-1.21,重大先天性畸形 RR=0.86,95%CI 0.47-1.56。在接受 MS 药物治疗的 MS 患者中,报告的最常见的重大先天性畸形为房间隔缺损(ASD)(N=4)、多指畸形(N=4)和马蹄内翻足(N=3),这些畸形在一般人群中是最常见的出生缺陷之一。总之,干扰素、聚乙二醇化干扰素β-1a 或那他珠单抗似乎不会增加自然流产、早产或重大先天性畸形的风险。有非常少的患者接受了芬戈莫德、硫唑嘌呤和利妥昔单抗治疗;因此,这些结果不能推广到所有药物。需要开展包括内部对照的未来研究,以便使治疗医生及其患者能够决定最佳的治疗选择。