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Adversity in childhood linked to elevated striatal dopamine function in adulthood
Alice Egerton1, Lucia R Valmaggia1, Oliver D Howes2
1King's College London, King's Health Partners, Institute of Psychiatry, Psychology and Neuroscience, De Crespigny Park, Denmark Hill, London SE5 8AF, UK.
Schizophrenia Research
|June 28, 2016
Summary
Childhood adversity, such as abuse or unstable family life, is linked to higher dopamine function in the brain
Area of Science:
- Neuroscience
- Psychiatry
- Dopamine Research
Background:
- Childhood adversity is a known risk factor for adult psychosis.
- Theoretical and animal models suggest dopamine dysregulation may mediate this link.
- Striatal dopamine function is implicated in psychosis development.
Purpose of the Study:
- To investigate the association between childhood adversity and striatal dopamine function in early adulthood.
- To compare childhood adversity exposure and dopamine function in individuals at ultra high risk (UHR) of psychosis versus healthy controls.
Main Methods:
- Sixty-seven young adults (47 UHR, 20 controls) underwent 18F-DOPA positron emission tomography to assess presynaptic dopamine function.
- Childhood adversity was measured using the Childhood Experience of Care and Abuse questionnaire.
- Participants were matched for age, gender, and substance use.
Main Results:
- Severe physical/sexual abuse and unstable family arrangements in childhood were significantly associated with elevated striatal dopamine function in adulthood.
- No significant differences in childhood adversity or dopamine function were found between the UHR and healthy volunteer groups.
- The overall sample demonstrated a link between childhood adversity and increased adult striatal dopamine function.
Conclusions:
- Childhood adversity is associated with altered striatal dopamine neurotransmission in adulthood.
- This finding supports the hypothesis that dopamine dysregulation may be a mechanism linking early life stress to psychosis risk.
- Further research is needed to explore the specific pathways and implications for psychosis prevention.
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