Evidence map›Paper›PMID 40938644›Full record

ReviewJournal of neuromuscular diseases2026

State of the art: Pregnancy in spinal muscular atrophy in the treatment era.

Maggie C Walter, Bernert Günther, Blaschek Astrid, Deschauer Marcus, Günther René, Hiebeler Miriam, Hahn Andreas, Kamm Christoph, Kirschner Janbernd, Lochmüller Hanns and 9 more

Abstract readReview
In one paragraph

Review in Journal of neuromuscular diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Maggie C WalterFriedrich Baur Institute, Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.
Bernert GüntherÖsterreichische Muskelforschung, Wien, Österreich.
Blaschek AstridLMU University Hospital, Department of Pediatrics, Division of Pediatric Neurology, MUC iSPZ Hauner, Munich University Center for Children with Medical and Developmental Complexity, Dr von Hauner Children's Hospital, Munich, Germany.
Deschauer MarcusDepartment of Neurology, Klinikum rechts der Isar, Technical University of Munich, School of Medicine and Health, Munich, Germany.
Günther RenéUniversity Hospital Carl Gustav Carus Dresden, Technische Universität Dresden, Dresden, Germany.
Hiebeler MiriamFriedrich Baur Institute, Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.
Hahn AndreasDepartment of Pediatric Neurology, Justus-Liebig-University, Giessen, Germany.
Kamm ChristophDept. of Neurology, University of Rostock, Rostock, Germany.
Kirschner JanberndDept. for Neuropediatrics and Muscle Disorders, Faculty of Medicine and Medical Center - University of Freiburg, Freiburg, Germany.
Lochmüller HannsChildren's Hospital of Eastern Ontario Research Institute, Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, Canada.
Löscher WolfgangDepartment of Neurology, Medical University Innsbruck, Innsbruck, Austria.
Müller-Felber WolfgangLMU University Hospital, Department of Pediatrics, Division of Pediatric Neurology, MUC iSPZ Hauner, Munich University Center for Children with Medical and Developmental Complexity, Dr von Hauner Children's Hospital, Munich, Germany.
Rudnik-Schöneborn SabineInstitute of Human Genetics, Medical University Innsbruck, Innsbruck, Austria.
Schara-Schmidt UlrikeDepartment of Neuropediatrics and Neuromuscular Centre for Children and Adolescents, Center for Translational Neuro- and Behavioral Sciences, Childreńs University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Thiele SimoneFriedrich Baur Institute, Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.
Uzelac ZeljkoDepartment of Neurology, Ulm University, Ulm, Germany.
Vill KatharinaLMU University Hospital, Department of Pediatrics, Division of Pediatric Neurology, MUC iSPZ Hauner, Munich University Center for Children with Medical and Developmental Complexity, Dr von Hauner Children's Hospital, Munich, Germany.ORCID 0000-0003-1925-7538
Weiler MarkusDepartment of Neurology, Heidelberg University Hospital, Heidelberg, Germany.
Hagenacker TimDepartment of Neurology, and Center for Translational Neuro- and Behavioral Sciences (C-TNBS), University Medicine Essen, Essen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An increasing number of adults with spinal muscular atrophy (SMA) wish to become parents. New disease-modifying therapies (DMT) have improved health outcomes and are expected to reduce disability in adults with SMA, but their current label prevents their use in pregnancy. While there is some information on pregnancy outcomes in the pre-DMT era, little has been published recently, and no ubiquitously accepted guidelines exist. Nonetheless, it is crucial to provide knowledgeable and open counselling, ideally in the context of treatments. Counseling for both adolescent and adult patients should include the subject of 'reproductive choices' when discussing the selection of DMTs for those considering parenthood. A multi-disciplinary team, including gynecologists and neurologists with expertise in neuromuscular disorders must closely monitor pregnant patients with SMA, preferably within disease registries, to detect potential complications early and ensure optimal treatment options are available. Real-world data in so far three patients with SMA showed a beneficial pregnancy outcome with nusinersen. It is anticipated that forthcoming real-world data will finally clarify the safety of administering Nusinersen during pregnancy, particularly in relation to child health and for preserving muscle function and preventing motor deterioration in the affected mother.

Indexed as

Muscular Atrophy, SpinalOligonucleotidesPregnancy ComplicationsFemaleHumansPregnancyPregnancy OutcomenusinersenOligonucleotidesdisease modifying treatmentnusinersenparenthoodpregnancyrisdiplamspinal muscular atrophy

Identifiers

PMID40938644
PMCPMC13442675

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.