Pregnancy and multiple sclerosis in the DMT era: A cohort study in Western Austria.


Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
01 2020
Historique:
pubmed: 7 12 2018
medline: 18 11 2020
entrez: 4 12 2018
Statut: ppublish

Résumé

Multiple sclerosis (MS) predominantly affects women of child-bearing potential. Pregnancy in MS is still a controversial issue lacking standardized treatment recommendations. To examine the reciprocal effects of pregnancy, MS, and disease-modifying treatment (DMT). We analyzed 387 pregnancies in 239 women with relapsing remitting multiple sclerosis (RRMS) and ⩾1 pregnancy, establishment of diagnosis >1 year before conception, and ⩾2 years of follow-up after delivery. Relapse rates and Expanded Disability Status Scale (EDSS) scores were compared in the year before conception, during pregnancy, and 2 years postpartum. Binary logistic regression was used to investigate predictors of risk for relapses and disability progression during pregnancy and postpartum. Risk of relapse and disability progression during pregnancy was predicted by pre-conception relapse activity, higher EDSS score at conception, use of highly effective disease-modifying treatment (H-DMT) pre-conception, and prolonged washout period. Postpartum relapse and disability progression was associated with relapse activity pre-conception and during pregnancy and use of H-DMT pre-conception. Early restart of DMT reduced the risk of postpartum relapse. A personalized approach in planning pregnancy in women with MS while on H-DMT needs to be adopted. It seems reasonable maintaining natalizumab closer to conception and restarting the drug early postpartum to reduce the considerable risk of disease reactivation during early pregnancy and after delivery.

Sections du résumé

BACKGROUND
Multiple sclerosis (MS) predominantly affects women of child-bearing potential. Pregnancy in MS is still a controversial issue lacking standardized treatment recommendations.
OBJECTIVE
To examine the reciprocal effects of pregnancy, MS, and disease-modifying treatment (DMT).
METHODS
We analyzed 387 pregnancies in 239 women with relapsing remitting multiple sclerosis (RRMS) and ⩾1 pregnancy, establishment of diagnosis >1 year before conception, and ⩾2 years of follow-up after delivery. Relapse rates and Expanded Disability Status Scale (EDSS) scores were compared in the year before conception, during pregnancy, and 2 years postpartum. Binary logistic regression was used to investigate predictors of risk for relapses and disability progression during pregnancy and postpartum.
RESULTS
Risk of relapse and disability progression during pregnancy was predicted by pre-conception relapse activity, higher EDSS score at conception, use of highly effective disease-modifying treatment (H-DMT) pre-conception, and prolonged washout period. Postpartum relapse and disability progression was associated with relapse activity pre-conception and during pregnancy and use of H-DMT pre-conception. Early restart of DMT reduced the risk of postpartum relapse.
CONCLUSION
A personalized approach in planning pregnancy in women with MS while on H-DMT needs to be adopted. It seems reasonable maintaining natalizumab closer to conception and restarting the drug early postpartum to reduce the considerable risk of disease reactivation during early pregnancy and after delivery.

Identifiants

pubmed: 30507345
doi: 10.1177/1352458518816614
doi:

Substances chimiques

Immunologic Factors 0
Natalizumab 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

69-78

Commentaires et corrections

Type : CommentIn

Auteurs

Gabriel Bsteh (G)

Clinical Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Laura Algrang (L)

Clinical Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Harald Hegen (H)

Clinical Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Michael Auer (M)

Clinical Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Sebastian Wurth (S)

Clinical Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Franziska Di Pauli (F)

Clinical Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Florian Deisenhammer (F)

Clinical Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Thomas Berger (T)

Clinical Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

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Classifications MeSH