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ArticleCurrent neuropharmacology2026

Maternal Multiple Sclerosis and Offspring's Developmental and Behavioral Profile: A Case-control Study.

Martina Siracusano, Doriana Landi, Elisa Carloni, Chiara Scoppola, Marialaura Ferrara, Assia Riccioni, Lucrezia Arturi, Leonardo Emberti Gialloreti, Mariagrazia Cicala, Francesca Napoli and 3 more

Abstract read
In one paragraph

Article in Current neuropharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

13 authors.

Martina SiracusanoDepartment of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0002-3357-1788
Doriana LandiDepartment of Systems Medicine, Multiple Sclerosis Clinical and Research Unit, Policlinico Tor Vergata, Tor Vergata University, Rome, Italy.
Elisa CarloniDepartment of Wellbeing of Mental and Neurological, Child Neurology and Psychiatry Unit, Dental and Sensory Organ Health, Policlinico Tor Vergata Hospital, Rome, Italy.
Chiara ScoppolaDepartment of Wellbeing of Mental and Neurological, Child Neurology and Psychiatry Unit, Dental and Sensory Organ Health, Policlinico Tor Vergata Hospital, Rome, Italy.
Marialaura FerraraDepartment of Wellbeing of Mental and Neurological, Child Neurology and Psychiatry Unit, Dental and Sensory Organ Health, Policlinico Tor Vergata Hospital, Rome, Italy.
Assia RiccioniDepartment of Wellbeing of Mental and Neurological, Child Neurology and Psychiatry Unit, Dental and Sensory Organ Health, Policlinico Tor Vergata Hospital, Rome, Italy.
Lucrezia ArturiDepartment of Wellbeing of Mental and Neurological, Child Neurology and Psychiatry Unit, Dental and Sensory Organ Health, Policlinico Tor Vergata Hospital, Rome, Italy.
Leonardo Emberti GialloretiDepartment of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
Mariagrazia CicalaDepartment of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
Francesca NapoliDepartment of Systems Medicine, Multiple Sclerosis Clinical and Research Unit, Policlinico Tor Vergata, Tor Vergata University, Rome, Italy.
Cinzia NioluDepartment of System Medicine, University of Rome Tor Vergata, Rome, Italy.
Luigi MazzoneDepartment of Wellbeing of Mental and Neurological, Child Neurology and Psychiatry Unit, Dental and Sensory Organ Health, Policlinico Tor Vergata Hospital, Rome, Italy.
Girolama Alessandra MarfiaDepartment of Systems Medicine, Multiple Sclerosis Clinical and Research Unit, Policlinico Tor Vergata, Tor Vergata University, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMaternal chronic immune and inflammatory conditions may predispose newborns to atypical developmental trajectories, identifying pregnancy as a key period for the etiopathogenesis of neurodevelopmental disorders. The possible long-term impact of maternal multiple sclerosis (MS) on the offspring's cognitive and behavioral development and its pharmacological treatment during pregnancy is mostly unknown. This study aims to delineate the cognitive and behavioral profile of offsprings exposed to maternal MS, untreated or treated with Natalizumab throughout pregnancy, in comparison to a control group.

methodsWe retrospectively enrolled 39 children (23 males; 16 females; mean age 45.82 ± 35.46 months) exposed to maternal MS, untreated or treated with Natalizumab throughout pregnancy, and 36 children (24 males; 12 females, mean age 38.03 ± 21.52 months) of healthy mothers. All offspring underwent a standardized evaluation of their intellectual or developmental quotient, adaptive functioning, and behavioral issues, including symptoms of autism.

resultsThe clinical profile of the included offspring was characterized by an adequate cognitive profile and a good level of adaptive skills (MS offspring: Griffiths III mean total DQ (N = 30) 114.57; WISC-IV mean Full IQs (N= 9) 115.44; mean ABAS GAC 97.28/Control offspring: Griffiths III mean total DQ (N = 31) 105.42; WISC-IV mean Full IQs (N= 4) 119.25 ± 11.32; mean ABAS GAC 97.82 ± 21.4). Furthermore, no significant behavioural problems or autism symptoms emerged in the entire group, regardless of MS treatment.

conclusionOffspring's developmental and behavioral phenotypes do not appear to be influenced by maternal treatment with Natalizumab until late pregnancy, nor by maternal variables directly related to MS (age at the time of MS diagnosis, disease duration, and severity).

Indexed as

Child DevelopmentMultiple SclerosisPregnancy ComplicationsPrenatal Exposure Delayed EffectsAdultCase-Control StudiesChild, PreschoolFemaleHumansMaleNatalizumabPregnancyRetrospective StudiesNatalizumabautismchildrenMultiple sclerosisnatalizumabneurodevelopmentpregnancy

Identifiers

PMID40621758
PMCPMC13269909

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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.