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Published on: November 21, 2013
Minor physical anomalies and vulnerability in prodromal youth
Vijay A Mittal1, Elaine F Walker
1Department of Psychology and Neuroscience, University of Colorado at Boulder, USA. vijay.mittal@colorado.edu
Insights
Minor physical anomalies (MPAs) in adolescents at high risk for psychosis are linked to higher cortisol, memory deficits, and disorganized symptoms. These findings suggest MPAs may indicate neural vulnerability in psychosis risk.
Area of Science:
- Neuroscience
- Developmental Psychology
- Psychiatry
Background:
- Minor physical anomalies (MPAs) arise from shared germinal layer origins with neural development.
- MPAs may indicate prenatal neural migration defects and brain abnormalities.
- Understanding MPA associations is crucial for psychosis etiology, particularly the neural diathesis-stress model.
Purpose of the Study:
- To investigate the relationship between MPAs and specific symptoms/characteristics in adolescents at high risk for psychosis.
- To explore MPAs as potential markers of vulnerability in psychosis development.
- To inform etiological models of psychosis.
Main Methods:
- Evaluated 50 adolescents with a prodromal syndrome.
- Assessed for minor physical anomalies (MPAs).
- Measured salivary cortisol, auditory and visual memory function, and attenuated positive, negative, and disorganized symptoms.
Main Results:
- Adolescents with elevated MPAs (n=25) showed higher salivary cortisol levels.
- Elevated MPAs were associated with deficits in immediate and delayed visual memory.
- Higher levels of disorganized prodromal symptoms were observed in participants with elevated MPAs.
Conclusions:
- Minor physical anomalies may serve as observable markers for underlying neural vulnerabilities.
- MPAs could indicate hippocampal system vulnerability in individuals with a prodromal psychosis syndrome.
- These findings support the utility of MPAs in identifying adolescents at heightened risk for psychosis.
Abstract:
Because both the brain and craniofacial/limb features originate from the same germinal layer during early gestation, the postnatal presence of minor physical anomalies (MPAs) involving these physical features may be indicative of defects in prenatal neural migration and consequent brain abnormalities among individuals with psychosis. However, to date it is unknown what symptoms and characteristics MPAs may be associated with, or how these markers may reflect vulnerability among adolescents at high-risk for developing psychosis. This information is particularly vital for understanding susceptibility and informing etiological conceptualizations such as the neural diathesis-stress model. In this study, 50 adolescents with a prodromal syndrome were evaluated for MPAs, salivary cortisol, auditory and visual memory function, and attenuated positive, negative, and disorganized symptoms. Results indicated that the participants showing elevated MPAs (n=25) were distinguished by elevated cortisol, deficit immediate and delayed visual memory, and higher levels of disorganized prodromal symptoms when compared with those participants exhibiting a lower incidence of MPAs. This was supported by supplementary correlational analyses examining the entire sample. These findings provide preliminary support for a theory that MPAs may reflect hippocampal system vulnerability among prodromal patients.
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