The Effects of Multiple Sclerosis and Disease Modifying Therapy on Pregnancy

Main Article Content

Tarneer Kaur Johal

Abstract

Abstract

Multiple sclerosis (MS) is the most common inflammatory condition of the central nervous system. Disease modifying therapy (DMT) aims to reduce relapse rates and decrease the quantity of lesions in the brain and spinal cord. Since MS is more prevalent in women than men, it is important to be aware of the interplay between MS and pregnancy. As MS can engender sexual dysfunction, primarily in the form of decreased desire and fatigue, it thereby affects conception. Hormonal differences between women with MS compared to women without MS include an increase in follicle-stimulating hormone and luteinizing hormone, and a decrease in testosterone. While fluctuations in estrogen result in a reduction in MS relapse rates during pregnancy, a subsequent increase in the post-partum period is observed. The mechanism of action and side effects of DMTs are described in this paper, including interferon, glatiramer acetate, and some newer medications. Although there are no recommended guidelines on the use of DMTs during pregnancy, it is generally agreed upon to cease their use prior to conception if possible, and the decision to continue a DMT should take into account the benefits to the mother and the risks to the fetus. Comprehending the mechanisms of action and teratogenicity indices of DMTs is crucial in understanding their effects on MS during pregnancy, which is an important aspect of providing health care to women with this condition. 

Résumé

La sclérose en plaques (SP) est l’affection inflammatoire du système nerveux central la plus commune. Le traitement modificateur de la maladie (DMT, de l’anglais) vise à réduire les taux de poussées et à diminuer le nombre de lésions au cerveau et à la moelle épinière. Comme la SP est plus prévalente chez les femmes que chez les hommes, il est important de reconnaître l’interaction entre la SP et la grossesse. Puisque la SP peut engendrer une dysfonction sexuelle, principalement en raison d’une diminution du désir sexuel et de la fatigue, elle affecte la conception. Les différences hormonales entre les femmes avec la SP et les femmes sans la SP incluent une hausse de l’hormone folliculostimulante et de l’hormone lutéinisante, et une baisse de testostérone. Bien que les fluctuations en œstrogènes entraînent en une réduction des taux de poussées de la SP durant la grossesse, leur augmentation subséquente lors de la période postpartum est observée. Le mécanisme d’action et les effets secondaires des DMTs sont décrits dans cet article, incluant l’interféron, l’acétate de glatiramère, et certains autres nouveaux médicaments. Quoiqu’il n’existe pas de lignes directrices sur l’utilisation des DMTs lors de la grossesse, il est généralement accepté qu’il faut cesser leur utilisation avant la conception si possible, et que la décision de continuer la prise d’un DMT devrait tenir compte des avantages pour la mère et des risques pour le fœtus. La compréhension des mécanismes d’action et des effets tératogènes des DMTs est essentielle pour apprécier leurs effets sur la SP durant la grossesse, ce qui constitue un aspect important dans la prestation des soins de santé aux femmes vivant avec cette maladie. 


Article Details

Section
Review & Clinical Practice
Author Biography

Tarneer Kaur Johal, University of British Columbia

MD Candidate 2018

Northern Medical Program

Year 3

University of British Columbia

 

References

1. Cordeau D, Courtois F. Sexual disorders in women with MS: Assessment and management. Ann Phys Rehabil Med. 2014;57(5):337-47.

2. Quinn H, Flood S, Mendelowitz E, Marrie RA, Foley FW. Predictors of fear of sexual rejection in individuals with multiple sclerosis. Sex Disabil. 2015;33(1):53-61.

3. Qaderi K, Merghati-Khoei E. Sexual problems and quality of life in women with multiple sclerosis. Sex Disabil. 2014;32(1):35-43.

4. Kolzet J, Quinn H, Zemon V, et al. Predictors of body image related sexual dysfunction in men and women with multiple sclerosis. Sex Disabil. 2015;33(1):63-73.

5. Gumus H, Akpinar Z, Yilmaz H. Effects of multiple sclerosis on female sexuality: A controlled study. J Sex Med. 2014;11(2):481-6.

6. Lúcio AC, D’Ancona CAL, Lopes MHBM, Perissinotto MC, Damasceno BP. The effect of pelvic floor muscle training alone or in combination with electro- stimulation in the treatment of sexual dysfunction in women with multiple sclerosis. Mult Scler. 2014;20(13):1761-8.

7. Lew-Starowicz M, Rola R. Prevalence of sexual dysfunctions among women with multiple sclerosis. Sex Disabil. 2013;31(2):141-53.

8. Schairer LC, Foley FW, Zemon V, et al. The impact of sexual dysfunction on health-related quality of life in people with multiple sclerosis. Mult Scler. 2014;20(5):610-16.

9. Amato MP, Portaccio E. Fertility, pregnancy and childbirth in patients with multiple sclerosis: Impact of disease-modifying drugs. CNS Drugs. 2015;29(3):207-20.

10. Grinsted L, Heltberg A, Hagen C, Djursing H. Serum sex hormone and go- nadotropin concentrations in premenopausal women with multiple sclerosis. J Intern Med. 1989;226(4):241-4.

11. Shahdaeizadeh S, Edalatmanesh MA, Moghadasi M. Evaluation of sex hormones (FSH, Estrogen and Testostrone) changes during follicular and luteal phases and sexual dysfunction in women with Multiple Sclerosis. J. Jahrom Univerisity Med Sci. 2014;12(4):26-39.

12. Foroughipour A, Norbakhsh V, Najafabadi SH, Meamar R. Evaluating sex hormone levels in reproductive age women with multiple sclerosis and their relationship with disease severity. J Res Med Sci. 2012;17(9):882-5.

13. Tomassini V, Onesti E, Mainero C, et al. Sex hormones modulate brain damage in multiple sclerosis: MRI evidence. J Neurol Neurosurg Psychiatry. 2005;76(2):272-5.

14. Eftekhari E, Etemadifar M, Mostahfezian M, Zafari A. Effects of resistance training and vibration on hormonal changes in female patients with multiple sclerosis. Neurol Asia. 2014;19(1):63-7.

15. Airas L. Hormonal and gender-related immune changes in multiple sclerosis. Acta Neurol Scand Suppl. 2015;132(199):62-70.

16. Sicotte NL, Liva SM, Klutch R, et al. Treatment of multiple sclerosis with the pregnancy hormone estriol. Ann Neurol. 2002;52(4):421-8.

17. Tan IJ, Peeva E, Zandman-Goddard G. Hormonal modulation of the immune system - A spotlight on the role of progestogens. Autoimmun Rev. 2015;14(6):536-42.

18. Yates MA, Li Y, Chlebeck P, Proctor T, Vandenbark AA, Offner H. Progesterone treatment reduces disease severity and increases IL-10 in experimental autoimmune encephalomyelitis. J Neuroimmunol. 2010;220(1-2):136-9.

19. Arnason BG. Interferon beta in multiple sclerosis. Neurol. 1993;43(4):641-3.

20. Sandberg-Wollheim M, Frank D, Goodwin TM, et al. Pregnancy out-comes during treatment with interferon beta-1a in patients with multiple sclerosis. Neurol. 2005;65(6):802-6.

21. Sandberg-Wollheim M, Alteri E, Moraga MS, Kornmann G. Pregnancy outcomes in multiple sclerosis following subcutaeous interferon beta-1a therapy. Mult Scler. 2011;17(4):423–30.

22. Lu E, Wang BW, Guimond C, Synnes A, Sadovnick D, Tremlett H. Disease-modifying drugs for multiple sclerosis in pregnancy: a systematic review. Neurology. 2012;79(11):1130-5.

23. Coyle PK. Multiple sclerosis and pregnancy presciptions. Expert Opin Drug Saf. 2014;13(12):1565-8.

24. Fragoso YD, Finkelsztejn A, Kaimen-Maciel DR, et al. Long-term use of glatiramer acetate by 11 pregnant women with multiple sclerosis: a retrospective, multicentre case series. CNS Drugs. 2010;24(11):969-76.

25. Karlsson G, Francis G, Koren G, et al. Pregnancy outcomes in the clinical development program of fingolimod in multiple sclerosis. Neurology. 2014;82(8):674-80.

26. Wehner NG, Shopp G, Rocca MS, Clarke J. Effects of natalizumab, an alpha4 integrin inhibitor, on the development of hartley guinea pigs. Birth Defects Res B Dev Reprod Toxicol. 2009;86(2):98-107.

27. Fox RJ, Cree BA, De Sèze J, et al. MS disease activity in RESTORE: a randomized 24-week natalizumab treatment interruption study. Neurology. 2014;82(17):1491-8.

28. Lebrun C, Le Page E, Kantarci O, Siva A, Pelletier D, Okuda DT. Impact of pregnancy on conversion to clinically isolated syndrome in a radiologically isolated syndrome cohort. Multi Scler. 2012;18(9):1297-1302.

29. De Santis M, Straface G, Cavaliere AF, Rosati P, Batocchi AP, Caruso A. The first case of mitoxantrone exposure in early pregnancy. Neurotoxicology. 2007;28(3):696–7.

30. Li J,Gold R,Fox R,et al. Delayed release dimethyl fumarate and pregnancy: Preclinical studies and pregnancy outcomes from clinical trials and post-marketing experience. Neurol. 2015;84(14):238.

31. Ghezz iA,Annovazzi P,Portaccio E,Cesari E,Amato MP.Current recommendations for multiple sclerosis treatment in pregnancy and puerperium. Expert Rev Clin Immunol. 2013;9(7):683-91.