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Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspring
BACKGROUND: Childhood neurodevelopmental disorders (NDDs), including specific learning disorders (SLD), attention deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD), are pathogenically linked to familial autoimmunity and maternal immune-mediated diseases during pregnancy. OBJEC...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165841/ https://www.ncbi.nlm.nih.gov/pubmed/34104473 http://dx.doi.org/10.1177/20552173211017301 |
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author | Carta, Alessandra Zarbo, Ignazio R Scoppola, Chiara Pisuttu, Giulia Conti, Marta Melis, Maria C Martino, Federica De Serra, Antonella Biancu, Maria A Guerini, Franca R Bazzardi, Riccardo Sotgiu, Stefano |
author_facet | Carta, Alessandra Zarbo, Ignazio R Scoppola, Chiara Pisuttu, Giulia Conti, Marta Melis, Maria C Martino, Federica De Serra, Antonella Biancu, Maria A Guerini, Franca R Bazzardi, Riccardo Sotgiu, Stefano |
author_sort | Carta, Alessandra |
collection | PubMed |
description | BACKGROUND: Childhood neurodevelopmental disorders (NDDs), including specific learning disorders (SLD), attention deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD), are pathogenically linked to familial autoimmunity and maternal immune-mediated diseases during pregnancy. OBJECTIVE: We studied maternal MS as a potential risk factor for NDDs occurrence in offspring. METHODS: MS and control mothers were subjected to questionnaires to ascertain NDD diagnosis in their progeny and the occurrence of both autoimmune and neurodevelopment disorders in their families. Suspected NDD cases were evaluated to confirm or rule out the diagnosis. RESULTS: Of the 322 MS women, 206 (64%) have 361 children; of these, 27 (7.5%) were diagnosed with NDD (11% ADHD; 22% ASD; 67% SLD). NDD-risk in offspring was associated to family history of autoimmunity and to NDDs both in MS and non-MS mother families (r = 0.75; p = 0.005) whereas it was not associated to maternal MS. CONCLUSIONS: For the first time, we demonstrate that maternal MS does not predispose children to higher risk for NDD. On a mechanistic view, we suggest that the intrinsic organ-specific nature of MS does not impair the mother–child cross-talk in decidua nor does it influence fetal neurodevelopment. |
format | Online Article Text |
id | pubmed-8165841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-81658412021-06-07 Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspring Carta, Alessandra Zarbo, Ignazio R Scoppola, Chiara Pisuttu, Giulia Conti, Marta Melis, Maria C Martino, Federica De Serra, Antonella Biancu, Maria A Guerini, Franca R Bazzardi, Riccardo Sotgiu, Stefano Mult Scler J Exp Transl Clin Original Research Paper BACKGROUND: Childhood neurodevelopmental disorders (NDDs), including specific learning disorders (SLD), attention deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD), are pathogenically linked to familial autoimmunity and maternal immune-mediated diseases during pregnancy. OBJECTIVE: We studied maternal MS as a potential risk factor for NDDs occurrence in offspring. METHODS: MS and control mothers were subjected to questionnaires to ascertain NDD diagnosis in their progeny and the occurrence of both autoimmune and neurodevelopment disorders in their families. Suspected NDD cases were evaluated to confirm or rule out the diagnosis. RESULTS: Of the 322 MS women, 206 (64%) have 361 children; of these, 27 (7.5%) were diagnosed with NDD (11% ADHD; 22% ASD; 67% SLD). NDD-risk in offspring was associated to family history of autoimmunity and to NDDs both in MS and non-MS mother families (r = 0.75; p = 0.005) whereas it was not associated to maternal MS. CONCLUSIONS: For the first time, we demonstrate that maternal MS does not predispose children to higher risk for NDD. On a mechanistic view, we suggest that the intrinsic organ-specific nature of MS does not impair the mother–child cross-talk in decidua nor does it influence fetal neurodevelopment. SAGE Publications 2021-05-28 /pmc/articles/PMC8165841/ /pubmed/34104473 http://dx.doi.org/10.1177/20552173211017301 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Paper Carta, Alessandra Zarbo, Ignazio R Scoppola, Chiara Pisuttu, Giulia Conti, Marta Melis, Maria C Martino, Federica De Serra, Antonella Biancu, Maria A Guerini, Franca R Bazzardi, Riccardo Sotgiu, Stefano Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspring |
title | Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspring |
title_full | Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspring |
title_fullStr | Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspring |
title_full_unstemmed | Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspring |
title_short | Maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspring |
title_sort | maternal multiple sclerosis is not a risk factor for neurodevelopmental disorders in offspring |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165841/ https://www.ncbi.nlm.nih.gov/pubmed/34104473 http://dx.doi.org/10.1177/20552173211017301 |
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