The outcomes of children born to mothers with autoimmune rheumatic diseases
- PMID: 38876127
- DOI: 10.1016/S2665-9913(24)00096-1
The outcomes of children born to mothers with autoimmune rheumatic diseases
Abstract
Maternal autoimmune rheumatic diseases can influence the outcomes of children through several life stages. During pregnancy, maternal inflammation and autoantibodies can hinder fetal development and lead to growth restriction, preterm birth, and low birth weight; prematurity, especially at extreme gestational ages, can in turn impair future child health. Treatment with compatible immunomodulatory drugs and preventive medications aims to keep maternal disease under control and minimise the risk of adverse pregnancy outcomes. However, concerns have been raised about the effects of immunomodulatory drugs on neonatal conditions (ie, the risk of serious infections, inadequate responses to vaccinations, and organ toxicity) and long-term outcomes (metabolic and cardiovascular problems and neurodevelopmental disorders). Among the unmet needs of parents with autoimmune rheumatic diseases, there is the estimation of risk for the children to develop autoimmune disorders and the need for reassurance about parenting capacity while living with a chronic condition. This Series paper provides a comprehensive overview of the literature and guidance on discussing these topics with patients.
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Conflict of interest statement
Declaration of interests LA reports consulting fees from UCB and speaking and writing fees from AlfaSigma, GSK, Janssen, Novartis, Pfizer, UCB, and the Werfen Group. JA is the Chair of Lupus Europe, which is funded mostly by grants or donations from pharmaceutical companies (Amgen/Horizon, AstraZeneca, Biogen, BMS, Boehringer Ingelheim, Galapagos, GSK, Idorsia, Janssen, Merck, Novartis, Otsuka, Roche, and UCB), none of which exceeds 25% of the total funds collected and none of whom have a say on the content of studies or work produced by Lupus Europe. TA reports consulting fees from Novartis and speaking and writing fees from AbbVie, Novartis, Pfizer, and Swedish Orphan Biovitrum. CDC reports research grants from Amgen, AstraZeneca, Genzyme Sanofi-Aventis, Gilead, GSK, Hoffman La-Roche-Genentech, Janssen, Leo Pharma, Novartis, Pfizer, Regeneron, Sanofi, Sun Pharma Global FZE, Takeda, the Gerber Foundation, and UCB. NM reports consulting fees as an expert advisor from RSM Consulting; speaking fees from Chiesi; and serves as a data safety monitoring board member in two National Institute for Health and Care Research Health Technology Assessment (NIHR HTA) trials and as the Trial Steering Committee Chair in a NIHR HTA trial. AT reports consulting fees from GSK and UCB and participated in advisory boards for Galapagos and UCB. All other authors declare no competing interest.
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