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Childhood abuse is associated with abnormalities in brain structure and function. Few studies have investigated abuse-related brain abnormalities in medication-naïve, drug-free youth that also controlled for psychiatric comorbidities by inclusion of a psychiatric control group, which is crucial to disentangle the effects of abuse from those associated with the psychiatric conditions.
Methods
Cortical volume (CV), cortical thickness (CT) and surface area (SA) were measured in 22 age- and gender-matched medication-naïve youth (aged 13–20) exposed to childhood abuse, 19 psychiatric controls matched for psychiatric diagnoses and 27 healthy controls. Both region-of-interest (ROI) and whole-brain analyses were conducted.
Results
For the ROI analysis, the childhood abuse group compared with healthy controls only, had significantly reduced CV in bilateral cerebellum and reduced CT in left insula and right lateral orbitofrontal cortex (OFC). At the whole-brain level, relative to healthy controls, the childhood abuse group showed significantly reduced CV in left lingual, pericalcarine, precuneus and superior parietal gyri, and reduced CT in left pre-/postcentral and paracentral regions, which furthermore correlated with greater abuse severity. They also had increased CV in left inferior and middle temporal gyri relative to healthy controls. Abnormalities in the precuneus, temporal and precentral regions were abuse-specific relative to psychiatric controls, albeit at a more lenient level. Groups did not differ in SA.
Conclusions
Childhood abuse is associated with widespread structural abnormalities in OFC–insular, cerebellar, occipital, parietal and temporal regions, which likely underlie the abnormal affective, motivational and cognitive functions typically observed in this population.
This chapter describes the clinical phenomenology and pathophysiology of Gilles de la Tourette syndrome (GTS) and reviews current structural and functional neuroimaging data of this fascinating neuropsychiatric condition. Significant neuroimaging evidence exists for a primary cortical dysfunction in GTS. Structural changes were reported in the basal ganglia, including both the striatum and the globus pallidus. Diffusion tensor imaging (DTI) has pointed to the microstructural abnormalities in white matter in GTS patients, including the corpus callosum and anterior and posterior limb of the internal capsule. Defects in brain maturation could be one of the pathophysiological mechanisms that lead to emergence of the GTS symptoms in childhood and their persistence into adulthood. Evidence from pharmacological trials, especially the fact that dopamine receptor blockers are the most effective treatment for tics to date, and postmortem analyses suggested that abnormalities of dopaminergic neurotransmission play a key role in the pathogenesis of GTS.
By
Colm McDonald, Institute of Psychiatry, King's College London, De Crespigny Park, London, UK,
Robin M. Murray, Institute of Psychiatry, King's College London, De Crespigny Park, London, UK
This chapter reviews the value of structural brain deviations identified through magnetic resonance imaging (MRI) as potential endophenotypes in genetic studies of schizophrenia and the evidence to date that a number of specific brain deviations are linked to susceptibility genes for schizophrenia from studies of patients and their unaffected relatives. One of the earliest studies of brain structure in normal twins was a computed tomographic (CT) study of subjects from the Maudsley Twin Series. In this study, measurements of ventricular volume in normal MZ twins were much more highly correlated than those of DZ twins, indicating strong genetic control over ventricular size, with estimates of heritability for ventricular size using different methods all over 80%. Despite heterogeneous patient samples and methodologies, neuroimaging studies consistently identify subtle volumetric deviations in a range of brain structures when schizophrenia patients are compared with controls.
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