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Updated: Dec 13, 2025

Author Spotlight: Studying the Impact of Maternal Dietary Deficiencies on Long-Term Offspring Health Outcomes
Published on: June 28, 2024
"APS pregnancy - The offspring"
Viktoria Bitsadze1, Cecilia Nalli2, Jamilya Khizroeva1
1Department of Obstetrics and Gynecology, I.M. Sechenov First Moscow State Medical University, Ministry of Health of the Russian Federation (Sechenov University), Moscow, Russia.
Insights
Antiphospholipid antibody syndrome (APS) in pregnant women can affect offspring, with potential risks including neonatal thrombosis and neurological issues. Long-term follow-up is crucial for monitoring developmental outcomes in these children.
Area of Science:
- Obstetrics and Gynecology
- Neonatology
- Immunology
Background:
- Antiphospholipid antibody syndrome (APS) is an autoimmune condition impacting women of childbearing age.
- Pregnancy management in APS has improved, but prematurity remains a concern due to placental effects of antiphospholipid antibodies (aPL).
- Maternal IgG aPL may cross the placenta, potentially affecting fetal brain development, though this is debated.
Observation:
- Neonatal thrombosis and minor neurological disorders have been reported in offspring of APS patients.
- Some neonatal thrombosis cases occurred without maternal aPL positivity, suggesting possible fetal/neonatal aPL synthesis.
- A case of neonatal catastrophic antiphospholipid syndrome (CAPS) was described.
Findings:
- Offspring of APS patients are generally healthy.
- However, risks of neonatal thrombosis and subtle neurological impairments exist.
Implications:
- Further research is needed due to limited data on aPL effects on offspring.
- Clinical follow-up of children born to mothers with APS is essential.
- Monitoring for neonatal thrombosis and long-term learning or behavioral issues is recommended.
Background:
Antiphospholipid antibody syndrome (APS) is an autoimmune disease that affects women in childbearing age. In recent years, great improvements were achieved in the management of pregnancies in these women. Prematurity could be an issue in these pregnancies, mainly due to the direct pathogenic effect of antiphospholipid antibodies (aPL) on the placental surface. Maternal IgG aPL can cross the placenta and theoretically interact with the growing fetus; it could reach the fetal brain because of the incompleteness of the fetal blood-brain barrier: whether this can have an effect on brain development is still debated. Neonatal thrombosis episodes have been described in children positive for aPL, not always associated with maternal antibody positivity, suggesting the hypothesis of a possible aPL de novo synthesis in fetus and neonates.
Methods:
A keyword-based literature search was conducted. We also described a case of neonatal catastrophic antiphospholipid syndrome (CAPS).
Results:
Offspring of patients with APS are generally healthy but the occurrence of neonatal thrombosis or minor neurological disorders were reported.
Conclusions:
The limited number of the available data on this sensitive issue supports the need for further studies. Clinical follow-up of children of mothers with APS seems to be important to exclude, in the neonatal period, the occurrence of aPL associated pathological events such as thrombosis, and in the long-term, impairment in learning skills or behavioral problems.
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