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Published on: March 2, 2018
Prenatal origins of neuropsychiatric diseases
Ariunzaya Amgalan1, Nickie Andescavage2,3, Catherine Limperopoulos3,4,5
1Georgetown School of Medicine, Washington, DC, USA.
Insights
Neuropsychiatric disorders may originate before birth due to intrauterine exposures. Research highlights prenatal imaging
Area of Science:
- Neuroscience
- Developmental Biology
- Psychiatry
Background:
- Evidence suggests neuropsychiatric diseases, including autism spectrum disorders (ASD) and schizophrenia, have origins in fetal development.
- Intrauterine factors like infection, hypoxia, and maternal health influence fetal brain development and disease risk.
Purpose of the Study:
- To review literature on the developmental origins of neuropsychiatric disorders.
- To explore the role of prenatal MR imaging in understanding fetal brain development and disease risk.
Main Methods:
- Literature review of human and animal studies.
- Discussion of advanced prenatal Magnetic Resonance (MR) imaging techniques.
Main Results:
- Strong evidence supports intrauterine origins for various neuropsychiatric conditions.
- Identified mechanisms of intrauterine injury impacting fetal brain development.
Conclusions:
- Fetal brain vulnerability to prenatal exposures increases risk for neuropsychiatric diseases like ASD and depression.
- Novel non-invasive imaging is crucial for studying fetal brain development.
- Emphasizing maternal health and postnatal monitoring is vital for early intervention.
Aim:
The main objective is to review the available evidence in the literature for developmental origins of neuropsychiatric diseases and their underlying mechanisms. We also probe emerging cutting-edge prenatal MR imaging tools and their future role in advancing our understanding the prenatal footprints of neuropsychiatric disorders.
Observations:
Both human and animal studies support early intrauterine origins of neuropsychiatric disease, particularly autism spectrum disorders (ASD), attention and hyperactivity disorders, schizophrenia, depression, anxiety and mood disorders. Specific mechanisms of intrauterine injury include infection, inflammation, hypoxia, hypoperfusion, ischaemia polysubstance use/abuse, maternal mental health and placental dysfunction.
Conclusions And Relevance:
There is ample evidence to suggest developmental vulnerability of the foetal brain to intrauterine exposures that increases and individual's risk for neuropsychiatric disease, especially the risk of ASD, depression and anxiety. Elucidating the exact timing and mechanisms of injury can be difficult and require novel, non-invasive approaches to the study emerging structural and functional brain development of the foetus. Clinical care should both emphasise maternal health during pregnancy, as well as close, continued monitoring for at risk offspring throughout young adulthood for the early identification and treatment of neuropsychiatric diseases.
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