Skip to main content
Log in

Glatiramer acetate exposure in pregnancy: preliminary safety and birth outcomes

  • Original Communication
  • Published:
Journal of Neurology Aims and scope Submit manuscript

Abstract

With the increasing incidence of multiple sclerosis (MS) in women and the earlier use of disease modifying therapy (DMT), issues surrounding DMT and pregnancy are a regular subject of discussion with regards to optimal management. Current recommendations are to withdraw DMT prior to conception, leaving patients exposed to an uncertain period of untreated disease. The objective of this study is to report preliminary experience on glatiramer acetate (GA) exposure through conception, pregnancy and the post-partum period in a series of 13 patients with previously highly active relapsing-remitting MS. This is a prospective observational case series. Fourteen pregnancies of 13 women resulted in 13 live births (one twin pregnancy), nine exposed to GA throughout pregnancy. There were no birth defects and treatment was well tolerated. No relapses occurred during pregnancy in those continuing on treatment. In conclusion, our early experience suggests that when considering the risks and benefits of treatment withdrawal prior to pregnancy, it may be reasonable to continue GA in those patients with previously highly active disease. Consideration should also be given to the initiation of a birth register, similar to such initiatives in epilepsy, to generate more robust safety data in this controversial area.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Fernandes LRA, Fernandes RP, Fragoso YD, Lippi UG (2007) Multiple sclerosis and pregnancy. Einstein 5:173–176

    Google Scholar 

  2. Lee M, O’Brien P (2008) Pregnancy and multiple sclerosis. J Neurol Neurosurg Psychiatry 79:1308–1311

    Article  CAS  PubMed  Google Scholar 

  3. Confavreux C, Hutchinson M, Hours MM, Cortinovis-Tourniaire P, Moreau T, Pregnancy in Multiple Sclerosis Group (1998) Rate of pregnancy-related relapse in multiple sclerosis. N Engl J Med 339:285–291

    Article  CAS  PubMed  Google Scholar 

  4. Saraste M, Ryynanen J, Alanen A, Multanen J, Farkkila M, Kaaja R, Airas L (2006) Cerebrospinal fluid findings in MS patients before, during, and after pregnancy. J Neurol Neurosurg Psychiatry 77:1195–1196

    Article  CAS  PubMed  Google Scholar 

  5. Vukusic S, Hutchinson M, Hours M, Moreau T, Cortinovis-Tourniaire P, Adeleine P, Confavreux C, The pregnancy in multiple sclerosis group (2004) Pregnancy and multiple sclerosis (The PRIMS study): clinical predictors of post-partum relapse. Brain 127:1353–1360

    Article  PubMed  Google Scholar 

  6. Boskovic R, Wide R, Wolpin J, Bauer DJ, Koren G (2005) The reproductive effects of beta interferon therapy in pregnancy: a longitudinal cohort. Neurology 65:807–811

    Article  CAS  PubMed  Google Scholar 

  7. Sandberg-Wollheim M, Frank D, Goodwin TM, Giesser B, Lopez-Bresnahan M, Stam-Moraga M et al (2005) Pregnancy outcomes during treatment with interferon beta-1a in patients with multiple sclerosis. Neurology 65:802–806

    Article  CAS  PubMed  Google Scholar 

  8. Putheti P, Soderstrom M, Link H, Huang YM (2003) Effects of glatiramer acetate (Copaxone) on CD4 + CD25 high T regulatory cells and their IL-10 production in multiple sclerosis. J Neuroimmunol 144:125–131

    Article  CAS  PubMed  Google Scholar 

  9. Coyle PK, Johnson K, Stark Y, Pardo L (2003) Pregnancy outcomes in patients with multiple sclerosis treated with glatiramer acetate (Copaxone). J Neurol Neurosurg Psychiatry 74:443 [poster]

    Google Scholar 

  10. Weber-Schoendorfer C, Schaefer C (2009) Multiple sclerosis, immunomodulators, and pregnancy outcome: a prospective observational study. Mult Scler 15:1037–1042

    Article  CAS  PubMed  Google Scholar 

  11. Ramtahal J, Jacob A, Das K, Boggild M (2006) Sequential treatment with glatiramer acetate after mitoxantrone is safe and can limit exposure to immunosuppression in very active, relapsing remitting MS. J Neurol 253:1160–1164

    Article  CAS  PubMed  Google Scholar 

  12. Miller A, DeAngelis T, Krieger S, Rooney-Crino A (2007) Use of glatiramer acetate during pregnancy: offering women a choice. Mult Scler 13: S7–S273 [abstract]

    Google Scholar 

  13. Ventura SJ, Martin JA, Curtin SC, Matthews TJ, Park MM (2000) Births: final data for 1998. Natl Vital Stat Rep 48:13–21

    Google Scholar 

  14. Adab N, Kini U, Vinten J, Ayres J, Baker G, Clayton-Smith J et al (2004) The longer term outcome of children born to mothers with epilepsy. J Neurol Neurosurg Psychiatry 75:1575–1583

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We would like to thank all the MS patients and their families for their participation in the study.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Heidi J. Salminen.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Salminen, H.J., Leggett, H. & Boggild, M. Glatiramer acetate exposure in pregnancy: preliminary safety and birth outcomes. J Neurol 257, 2020–2023 (2010). https://doi.org/10.1007/s00415-010-5652-y

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00415-010-5652-y

Keywords

Navigation