Four Years On: Pregnancy and Birth Outcomes Reported in the MSBase Pregnancy, Neonatal Outcomes, and Women’s Health Registry (2020–2024)
| dc.contributor.author | Jokubaitis, Vilija G. | |
| dc.contributor.author | Alroughani, Raed A. | |
| dc.contributor.author | Altintaş, Ayşe | |
| dc.contributor.author | Eichau, Sara | |
| dc.contributor.author | Hughes, Stella E. | |
| dc.contributor.author | Willekens, Barbara | |
| dc.contributor.author | Boz, Cavit | |
| dc.contributor.author | Kopchak, Oksana | |
| dc.contributor.author | Gray, Orla | |
| dc.date.accessioned | 2025-07-25T16:37:52Z | |
| dc.date.available | 2025-07-25T16:37:52Z | |
| dc.date.issued | 2025-07-07 | |
| dc.description.abstract | Background: Family planning is an important aspect of multiple sclerosis (MS), and neuromyelitis optica spectrum disorder (NMOSD) management. Knowledge gaps remain, including optimal perinatal management strategies, and fetal risks associated with disease-modifying therapy (DMT) exposure. Objective: To describe perinatal DMT use, together with pregnancy and neonatal outcomes prospectively recorded in the International MSBase Pregnancy and Women’s Health Registry. Methods: We report summary statistics for data collected between May 2020 and August 2024. Results: A total of 1887 relapsing-remitting MS (RRMS), 12 primary-progressive MS (PPMS), 2 radiologically isolated syndrome (RIS) and 21 NMOSD completed pregnancies were recorded, including 1644 (85.5%) live births, 208 (10.8%) miscarriages, and 6 (0.3%) neonatal deaths. Most women had unassisted (53.8%) or assisted (7.4%) vaginal births. Seventy five percent of pregnancies had DMT exposures within 6 months preconception; 19% of NMOSD, and 62% of MS pregnancies were DMT-exposed during gestation; 18.1% of pregnancies reported in-pregnancy monoclonal antibody DMT exposure. No overt safety signals were seen. Conclusion: This first report from the newly launched MSBase pregnancy registry, establishes an increasing number of pregnancies being conceived on monoclonal antibody therapies. Although no safety signals were observed, it is important to continue monitoring for safety signals in real-world databases as the use of highly effective therapies continues to increase perinatally. © 2025 Elsevier B.V., All rights reserved. | en_US |
| dc.description.sponsorship | AVDW served on advisory boards and receives unrestricted research grants from Novartis, Biogen, Merck, and Roche She has received speaker’s honoraria and travel support from Novartis, Roche, and Merck. She receives grant support from the National Health and Medical Research Council of Australia and MS Research Australia. | |
| dc.description.sponsorship | Biogen; Merck; Novartis; Roche | |
| dc.description.sponsorship | EKH received honoraria/research support from Biogen, Merck Serono, Novars, Roche, and Teva; has been member of advisory boards for Actelion, Biogen, Celgene, Merck Serono, Novars, and Sanofi Genzyme; received honoraria/research support from Biogen, Merck Serono, Novars, Roche, and Teva; has been member of advisory boards for Actelion, Biogen, Celgene, Merck Serono, Novars, and Sanofi Genzyme; and has been supported by the Czech Ministry of Education—project Cooperation LF1, research area Neuroscience, and the project National Institute for Neurological Research (Programme EXCELES, ID project No LX22NPO5107)—funded by the European Union-Next Generation EU. | |
| dc.description.sponsorship | MS Australia; MS Research Australia; Novartis; Monash University; Teva; Teva Pharma; Czech Ministry of Education; Roche; NHMRC Australia; Merck; NHMRC; Sanofi Genzyme; Genzyme; Queen Elisabeth Medical Foundation for Neurosciences; FWO-TBM; Bristol-Myers Squibb; F. Hoffmann-La Roche; Pennycook Foundation; Belgian Charcot Foundation; Trish MS Foundation; European Union-Next Generation EU; Start2Cure Foundation; Janssen-Cilag; Biogen; National MS Society; Trish Multiple Sclerosis Research Foundation; European Union; National Health and Medical Research Council, NHMRC, (2025360); National Health and Medical Research Council, NHMRC; National Institute for Neurological Research, (LX22NPO5107); General University Hospital in Prague, (MH CZ-DRO-VFN64165) | |
| dc.description.sponsorship | MP received honoraria and travel grants from the following pharmaceutical companies: Biogen, Bristol-Myers Squibb, Genzyme, Janssen-Cilag, Merck Serono, Novartis, Roche, and Teva Pharma. | |
| dc.description.sponsorship | The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: VGJ Receives research fellowship support from the National Health and Medical Research Council of Australia (2025360). Her institution receives research funding support from F.Hoffmann-La Roche, the International Progressive MS Alliance, Multiple Sclerosis Australia and the Pennycook Foundation outside of this current work. She has received speaker’s honoraria from Novartis and The Limbic. | |
| dc.description.sponsorship | ZP received honoraria and travel grants from the following pharmaceutical companies: Biogen, Bristol-Myers Squibb, Eli Lilly, Genzyme, Janssen-Cilag, Lundbeck, Merck Serono, Novartis, Roche, and Teva Pharma. | |
| dc.description.sponsorship | DH was supported by the Charles University: Cooperation Program in Neuroscience, by the project National Institute for Neurological Research (Programme EXCELES, ID Project No. LX22NPO5107)—Funded by the European Union—Next Generation EU, and by General University Hospital in Prague project MH CZ-DRO-VFN64165. She also received compensation for travel, speaker honoraria and consultant fees from Biogen Idec, Novartis, Merck, Bayer, Sanofi Genzyme, Roche, and Teva, as well as support for research activities from Biogen Idec. | |
| dc.description.sponsorship | HB is an employee of Monash University and has accepted travel compensation from Merck; his institution receives honoraria for talks, steering committee activities, and research grants from Roche, Merck, Biogen, Novartis, and UCB Pharma, Medical Research Future Fund Australia, NHMRC Australia, Trish MS Foundation, MS Australia and the Pennycook Foundation. He receives personal compensation for steering group activities for the Brain Health Initiative from Oxford Health Policy Forum and is funded by an NHMRC Australia Investigator Grant. | |
| dc.description.sponsorship | IR served on scientific advisory boards, received conference travel support and/or speaker honoraria from Roche, Novartis, Merck and Biogen. Izanne Roos is supported by MS Australia and the Trish Multiple Sclerosis Research Foundation. | |
| dc.description.sponsorship | The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The study did not receive specific funding support. The MSBase Registry receives financial support from Biogen, Merck, Novartis and Roche. | |
| dc.description.sponsorship | BW received honoraria for acting as a member of Scientific Advisory Boards/Consultancy for Alexion, Almirall, Biogen, Celgene/BMS, Merck, Janssen, Novartis, Roche, Sandoz, Sanofi Genzyme and speaker honoraria and travel support from Biogen, Celgene/BMS, Merck, Novartis, Roche, Sanofi Genzyme; research and/or patient support grants from Biogen, Janssen, Merck, Sanofi Genzyme, Roche. Honoraria and grants were paid to the UZA/UZA Foundation. Further, B.W. received research funding from FWO-TBM, Belgian Charcot Foundation, Start2Cure Foundation, Queen Elisabeth Medical Foundation for Neurosciences, and the National MS Society USA. | |
| dc.identifier.doi | 10.1177/13524585251349125 | |
| dc.identifier.issn | 1352-4585 | |
| dc.identifier.issn | 1477-0970 | |
| dc.identifier.scopus | 2-s2.0-105013333645 | |
| dc.identifier.uri | https://doi.org/10.1177/13524585251349125 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14365/6299 | |
| dc.language.iso | en | en_US |
| dc.publisher | SAGE Publications Ltd | en_US |
| dc.relation.ispartof | Multiple Sclerosis Journal | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Disease-Modifying Therapy | en_US |
| dc.subject | Multiple Sclerosis | en_US |
| dc.subject | Neonatal Outcomes | en_US |
| dc.subject | Neuromyelitis Optica Spectrum Disorder | en_US |
| dc.subject | Pregnancy | en_US |
| dc.subject | Immunologic Factors | en_US |
| dc.subject | Immunologic Factor | en_US |
| dc.subject | Adult | en_US |
| dc.subject | Drug Therapy | en_US |
| dc.subject | Epidemiology | en_US |
| dc.subject | Female | en_US |
| dc.subject | Human | en_US |
| dc.subject | Multiple Sclerosis | en_US |
| dc.subject | Myelooptic Neuropathy | en_US |
| dc.subject | Newborn | en_US |
| dc.subject | Pregnancy | en_US |
| dc.subject | Pregnancy Complication | en_US |
| dc.subject | Pregnancy Outcome | en_US |
| dc.subject | Register | en_US |
| dc.subject | Relapsing Remitting Multiple Sclerosis | en_US |
| dc.subject | Young Adult | en_US |
| dc.subject | Adult | en_US |
| dc.subject | Female | en_US |
| dc.subject | Humans | en_US |
| dc.subject | Immunologic Factors | en_US |
| dc.subject | Infant, Newborn | en_US |
| dc.subject | Multiple Sclerosis | en_US |
| dc.subject | Multiple Sclerosis, Relapsing-Remitting | en_US |
| dc.subject | Neuromyelitis Optica | en_US |
| dc.subject | Pregnancy | en_US |
| dc.subject | Pregnancy Complications | en_US |
| dc.subject | Pregnancy Outcome | en_US |
| dc.subject | Registries | en_US |
| dc.subject | Young Adult | en_US |
| dc.title | Four Years On: Pregnancy and Birth Outcomes Reported in the MSBase Pregnancy, Neonatal Outcomes, and Women’s Health Registry (2020–2024) | en_US |
| dc.type | Article | en_US |
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| gdc.author.id | Surcinelli, Andrea/0000-0003-3779-0934 | |
| gdc.author.id | Jokubaitis, Vilija/0000-0002-3942-4340 | |
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| gdc.description.departmenttemp | [Jokubaitis] Vilija G., Department of Neuroscience, Monash University, Melbourne, Australia, Department of Neurology, Alfred Health, Melbourne, Australia; [Alroughani] Raed A., Al-Amiri Hospital, Safat, Kuwait; [Altintaş] Ayşe, Koç Üniversitesi, Istanbul, Turkey; [Eichau] Sara, Hospital Universitario Virgen Macarena, Sevilla, Spain; [Hughes] Stella E., Royal Victoria Hospital Belfast, Belfast, United Kingdom; [Willekens] Barbara, Department of Neurology, Universitair Ziekenhuis Antwerpen, Edegem, Belgium; [Horáková] Dana, Department of Neurology and Center of Clinical Neuroscience, Všeobecná Fakultní Nemocnice v Praze, Prague, Czech Republic; [Kubala Havrdová] Eva Kubala, Department of Neurology and Center of Clinical Neuroscience, Všeobecná Fakultní Nemocnice v Praze, Prague, Czech Republic; [Özakbaş] Serkan, Medical Point Hospital, Izmir Ekonomi Üniversitesi, Izmir, Turkey, Multiple Sclerosis Research Association, Izmir, Turkey; [Boz] Cavit, Department of Neurology, Karadeniz Technical University, Trabzon, Turkey | en_US |
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