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Neuropsychiatric Outcome of Children Born to Women With Systemic Lupus Erythematosus and Exposed in Utero to Azathioprine: A Case-Control Study

Objective: The long-term outcome of children born to SLE mothers still represents a controversial topic in literature, with some studies reporting a possible increased prevalence of different neurologic and psychiatric diseases (NPD), including neurodevelopmental disorders (ND), and in particular le...

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Autores principales: Lazzaroni, Maria-Grazia, Andreoli, Laura, Crisafulli, Francesca, Tamborini, Francesco, Debeni, Irene, Binda, Valentina, Nalli, Cecilia, Galli, Jessica, Fazzi, Elisa, Moroni, Gabriella, Franceschini, Franco, Tincani, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7772243/
https://www.ncbi.nlm.nih.gov/pubmed/33390998
http://dx.doi.org/10.3389/fphar.2020.613239
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author Lazzaroni, Maria-Grazia
Andreoli, Laura
Crisafulli, Francesca
Tamborini, Francesco
Debeni, Irene
Binda, Valentina
Nalli, Cecilia
Galli, Jessica
Fazzi, Elisa
Moroni, Gabriella
Franceschini, Franco
Tincani, Angela
author_facet Lazzaroni, Maria-Grazia
Andreoli, Laura
Crisafulli, Francesca
Tamborini, Francesco
Debeni, Irene
Binda, Valentina
Nalli, Cecilia
Galli, Jessica
Fazzi, Elisa
Moroni, Gabriella
Franceschini, Franco
Tincani, Angela
author_sort Lazzaroni, Maria-Grazia
collection PubMed
description Objective: The long-term outcome of children born to SLE mothers still represents a controversial topic in literature, with some studies reporting a possible increased prevalence of different neurologic and psychiatric diseases (NPD), including neurodevelopmental disorders (ND), and in particular learning disorders (LD). Different risk factors have been advocated, such as the in utero exposure to auto-antibodies and drugs, particularly Azathioprine (AZA). Methods: A case-control study was designed to compare pregnancies treated with AZA (cases) with those not treated with AZA (controls). All the pregnancies had been prospectively followed in two Italian centers. The match was based upon renal involvement, antiphospholipid (aPL) status, maternal age at pregnancy (±5 years) and child’s age at the time of the study (±2 years). SLE mothers were interviewed by a telephone survey, particularly focused on the presence of a certified NPD in their children ≥6 years of age. Results: Twenty-seven cases and 65 controls were similar in terms of demographic, immunological and clinical features, except for a higher rate of SLE flares during pregnancy in cases (22.2% vs. 10.8%, p:0.191). The 92 children had a mean age of 14.0 years at the time of the survey; 11 had at least one NPD (12.0%). The frequency of each single NPD was similar to that of the general pediatric population and no association was found with either the in utero exposure to AZA, or other specific factors (auto-antibodies, disease activity, obstetric complications, prematurity). Conclusion: The long-term neuropsychiatric outcome of the children born to SLE mothers did not show neither an increased frequency of NPD as compared to the general pediatric population nor a specific pattern of NPD. The in utero exposure to AZA was not associated with the development of NPD in this case-control study of prospectively-followed pregnancies. NPD are complex conditions and large prospective studies are needed to capture the wide range of variables that may contribute to their development in the offspring of SLE women.
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spelling pubmed-77722432020-12-31 Neuropsychiatric Outcome of Children Born to Women With Systemic Lupus Erythematosus and Exposed in Utero to Azathioprine: A Case-Control Study Lazzaroni, Maria-Grazia Andreoli, Laura Crisafulli, Francesca Tamborini, Francesco Debeni, Irene Binda, Valentina Nalli, Cecilia Galli, Jessica Fazzi, Elisa Moroni, Gabriella Franceschini, Franco Tincani, Angela Front Pharmacol Original Research Objective: The long-term outcome of children born to SLE mothers still represents a controversial topic in literature, with some studies reporting a possible increased prevalence of different neurologic and psychiatric diseases (NPD), including neurodevelopmental disorders (ND), and in particular learning disorders (LD). Different risk factors have been advocated, such as the in utero exposure to auto-antibodies and drugs, particularly Azathioprine (AZA). Methods: A case-control study was designed to compare pregnancies treated with AZA (cases) with those not treated with AZA (controls). All the pregnancies had been prospectively followed in two Italian centers. The match was based upon renal involvement, antiphospholipid (aPL) status, maternal age at pregnancy (±5 years) and child’s age at the time of the study (±2 years). SLE mothers were interviewed by a telephone survey, particularly focused on the presence of a certified NPD in their children ≥6 years of age. Results: Twenty-seven cases and 65 controls were similar in terms of demographic, immunological and clinical features, except for a higher rate of SLE flares during pregnancy in cases (22.2% vs. 10.8%, p:0.191). The 92 children had a mean age of 14.0 years at the time of the survey; 11 had at least one NPD (12.0%). The frequency of each single NPD was similar to that of the general pediatric population and no association was found with either the in utero exposure to AZA, or other specific factors (auto-antibodies, disease activity, obstetric complications, prematurity). Conclusion: The long-term neuropsychiatric outcome of the children born to SLE mothers did not show neither an increased frequency of NPD as compared to the general pediatric population nor a specific pattern of NPD. The in utero exposure to AZA was not associated with the development of NPD in this case-control study of prospectively-followed pregnancies. NPD are complex conditions and large prospective studies are needed to capture the wide range of variables that may contribute to their development in the offspring of SLE women. Frontiers Media S.A. 2020-12-16 /pmc/articles/PMC7772243/ /pubmed/33390998 http://dx.doi.org/10.3389/fphar.2020.613239 Text en Copyright © 2020 Lazzaroni, Andreoli, Crisafulli, Tamborini, Debeni, Binda, Nalli, Galli, Fazzi, Moroni, Franceschini and Tincani http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Original Research
Lazzaroni, Maria-Grazia
Andreoli, Laura
Crisafulli, Francesca
Tamborini, Francesco
Debeni, Irene
Binda, Valentina
Nalli, Cecilia
Galli, Jessica
Fazzi, Elisa
Moroni, Gabriella
Franceschini, Franco
Tincani, Angela
Neuropsychiatric Outcome of Children Born to Women With Systemic Lupus Erythematosus and Exposed in Utero to Azathioprine: A Case-Control Study
title Neuropsychiatric Outcome of Children Born to Women With Systemic Lupus Erythematosus and Exposed in Utero to Azathioprine: A Case-Control Study
title_full Neuropsychiatric Outcome of Children Born to Women With Systemic Lupus Erythematosus and Exposed in Utero to Azathioprine: A Case-Control Study
title_fullStr Neuropsychiatric Outcome of Children Born to Women With Systemic Lupus Erythematosus and Exposed in Utero to Azathioprine: A Case-Control Study
title_full_unstemmed Neuropsychiatric Outcome of Children Born to Women With Systemic Lupus Erythematosus and Exposed in Utero to Azathioprine: A Case-Control Study
title_short Neuropsychiatric Outcome of Children Born to Women With Systemic Lupus Erythematosus and Exposed in Utero to Azathioprine: A Case-Control Study
title_sort neuropsychiatric outcome of children born to women with systemic lupus erythematosus and exposed in utero to azathioprine: a case-control study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7772243/
https://www.ncbi.nlm.nih.gov/pubmed/33390998
http://dx.doi.org/10.3389/fphar.2020.613239
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