Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Sep;5(5):247-53.
doi: 10.1177/1756285612453192.

Multiple sclerosis and pregnancy: experience from a nationwide database in Germany

Affiliations

Multiple sclerosis and pregnancy: experience from a nationwide database in Germany

Kerstin Hellwig et al. Ther Adv Neurol Disord. 2012 Sep.

Abstract

Objective: The objective of this study was to evaluate exposure to disease-modifying therapies (DMTs) during pregnancy in 335 pregnancies of multiple sclerosis (MS) patients and to further determine whether exclusive breastfeeding of MS mothers has any relevant influence on postpartum relapse rate.

Background: Only limited data are available on whether DMT exposure during pregnancy affects relapse rate during pregnancy or after birth. Currently, findings on beneficial effect of exclusive breastfeeding on MS disease course are controversially discussed.

Methods: We enrolled pregnant women with MS who contacted us directly or via their treating physicians to be included in our nationwide MS and pregnancy database.

Results: We identified 78 pregnancies under interferon-beta (IFNβ) preparations, 41 under glatiramer acetate (GLAT), and 216 pregnancies without DMT exposure during pregnancy. As expected, annualized relapse rate (ARR) decreased continuously during pregnancy in nonexposed mothers (p < 0.001) to then increase after birth. In IFNβ- or GLAT-exposed women this typical pattern was not as obvious. Congenital anomalies were within normal ranges in exposed pregnancies. In total, 170 women were identified who exclusively breastfed (EBF). Significantly reduced postpartum relapse rate during the first 3 months after birth were registered in the EBF group as compared with nonexclusively breastfeeding (NEBF) or nonbreastfeeding women (NBF) women with MS (p < 0.0001). Relapse rate (RR) in the year before pregnancy had been similar throughout all groups. We did not observe any significant differences in RR of NEBF and NBF women.

Conclusion: Exclusive breastfeeding showed some beneficial effects on postpartum relapse rate in our cohort. Our data support that IFNβ and GLAT do not seem to represent a major teratogenic risk in pregnancy.

Keywords: breastfeeding; disease-modifying therapy (DMT); relapse rate.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest statement: This MS and pregnancy database was partly supported by Bayer-Schering Healthcare, Biogen-Idec Germany, Merck-Serono, Teva Pharma, Novartis Pharma and Sanofi Aventis. Dr Hellwig has received speakers honoraria and research support from Bayer-Schering Healthcare, Biogen-Idec Germany, Merck-Serono, Teva Pharma, Novartis Pharma and Sanofi Aventis. Dr Haghikia has received limited research support from Biogen Idec and speakers honoraria from Bayer Healthcare, Biogen Idec, Teva and Merck Serono. Milena Rockhoff has nothing to disclose. Professor Gold has received speakers honoraria and research support from Bayer-Schering Healthcare, Biogen-Idec Germany, Merck-Serono, Teva Pharma, Novartis Pharma and Sanofi Aventis.

Figures

Figure 1.
Figure 1.
Annual relapse rate before and during pregnancy. I, II, III = I, II, III Trimester, ARR = annual relapse rate. * = p < 0.05, ** = p < 0.01; *** = p < 0.001 of the comparison ARR before versus ARR I respectively, ARR II, ARR III; data are given as mean ± SD.
Figure 2.
Figure 2.
Annual relapse rate in the first trimester postpartum according to breastfeeding status.RR = relapse rate. *** = p < 0.001 data are given as mean ± SD.

References

    1. Airas L., Jalkanen A., Alanen A., Pirttila T., Marttila R. (2010) Breast-feeding, postpartum and prepregnancy disease activity in multiple sclerosis. Neurology 75: 474–476 - PubMed
    1. Amato M., Portaccio E., Ghezzi A., Hakiki B., Zipoli V., Martinelli V., et al. (2010) Pregnancy and fetal outcomes after interferon-beta exposure in multiple sclerosis. Neurology 75: 1794–1802 - PubMed
    1. Boskovic R., Wide R., Wolpin J., Bauer D., Koren G. (2005) The reproductive effects of beta interferon therapy in pregnancy: a longitudinal cohort. Neurology 65: 807–811 - PubMed
    1. Comi G., Filippi M., Wolinsky J. (2001) European/Canadian multicenter, double-blind, randomized, placebo-controlled study of the effects of glatiramer acetate on magnetic resonance imaging-measured disease activity and burden in patients with relapsing multiple sclerosis. European/Canadian Glatiramer Acetate Study Group; Ann Neurol 49: 290–297 - PubMed
    1. Confavreux C., Hutchinson M., Hours M., Cortinovis-Tourniaire P., Moreau T. (1998) Rate of pregnancy-related relapse in multiple sclerosis. Pregnancy in Multiple Sclerosis Group; N Engl J Med 339: 285–291 - PubMed