A systematic review and meta-analyses of pregnancy and fetal outcomes in women with multiple sclerosis: a contribution from the IMI2 ConcePTION project.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 23 01 2020
accepted: 18 03 2020
revised: 17 03 2020
pubmed: 24 5 2020
medline: 22 6 2021
entrez: 24 5 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 32444984
doi: 10.1007/s00415-020-09913-1
pii: 10.1007/s00415-020-09913-1
pmc: PMC7419441
doi:

Substances chimiques

Natalizumab 0
Glatiramer Acetate 5M691HL4BO

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2721-2731

Subventions

Organisme : Innovative Medicines Initiative 2
ID : 821520

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Auteurs

Sandra Lopez-Leon (S)

Novartis Pharmaceuticals Corporation, One Health Plaza, Building 339-1131, East Hanover, NJ, 07936-1080, USA. sandra.lopez@novartis.com.

Yvonne Geissbühler (Y)

Novartis Pharma AG, Basel, Switzerland.

Meritxell Sabidó (M)

Global Epidemiology, Merck KGaA, Darmstadt, Germany.

Moise Turkson (M)

Cognizant Solution, London, UK.

Charlotte Wahlich (C)

Population Health Research Institute, St George's, University of London, London, UK.

Joan K Morris (JK)

Population Health Research Institute, St George's, University of London, London, UK. jmorris@sgul.ac.uk.

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Classifications MeSH