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1.
Brain Res ; 1479: 1-16, 2012 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-22902768

RESUMO

Abnormalities in structural and functional connectivity have been reported in autism spectrum disorders (ASD) across a wide age range. However, developmental changes in white matter microstructure are poorly understood. We used a cross-sectional design to determine whether white matter abnormalities measured using diffusion tensor imaging (DTI) were present in adolescents and adults with ASD and whether age-related changes in white matter microstructure differed between ASD and typically developing (TD) individuals. Participants included 28 individuals with ASD and 33 TD controls matched on age and IQ and assessed at one time point. Widespread decreased fractional anisotropy (FA), and increased radial diffusivity (RaD) and mean diffusivity (MD) were observed in the ASD group compared to the TD group. In addition, significant group-by-age interactions were observed in FA, RaD, and MD in all major tracts except the brain stem, indicating that age-related changes in white matter microstructure differed between the groups. We propose that white matter microstructural changes in ASD may reflect myelination and/or other structural differences including differences in axonal density/arborization. In addition, we suggest that white matter microstuctural impairments may be normalizing during young adulthood in ASD. Future longitudinal studies that include a wider range of ages and more extensive clinical characterization will be critical for further uncovering the neurodevelopmental processes unfolding during this dynamic time in development.


Assuntos
Transtornos Globais do Desenvolvimento Infantil/diagnóstico , Transtornos Globais do Desenvolvimento Infantil/patologia , Fibras Nervosas Mielinizadas/patologia , Adolescente , Adulto , Fatores Etários , Criança , Transtornos Globais do Desenvolvimento Infantil/metabolismo , Imagem de Difusão por Ressonância Magnética/métodos , Feminino , Humanos , Masculino , Fibras Nervosas Mielinizadas/metabolismo , Adulto Jovem
2.
Obes Facts ; 5(2): 243-53, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22647305

RESUMO

OBJECTIVE: To use functional magnetic resonance imaging (fMRI) in craniopharyngioma (CP) patients to examine the hypothesis that hypothalamic damage due to CP and its treatment results in enhanced perception of food reward and/or impaired central satiety processing. METHODS: Pre- and post-meal responses to visual food cues in brain regions of interest (ROI; bilateral nucleus accumbens, bilateral insula, and medial orbitofrontal cortex) were assessed in 4 CP patients versus 4 age- and weight-matched controls. Stimuli consisted of images of high- ('fattening') and low-calorie ('non-fattening') foods in blocks, alternating with non-food object blocks. After the first fMRI scan, subjects drank a high-calorie test meal to suppress appetite, then completed a second fMRI scan. Within each ROI, we calculated mean z-scores for activation by fattening as compared to non-fattening food images. RESULTS: Following the test meal, controls showed suppression of activation by food cues while CP patients showed trends towards higher activation. CONCLUSION: These data, albeit in a small group of patients, support our hypothesis that perception of food cues may be altered in hypothalamic obesity (HO), especially after eating, i.e. in the satiated state. The fMRI approach is encouraging for performing future mechanistic studies of the brain response to food cues and satiety in patients with hypothalamic or other forms of childhood obesity.


Assuntos
Craniofaringioma/psicologia , Dieta/psicologia , Obesidade/psicologia , Percepção/fisiologia , Neoplasias Hipofisárias/psicologia , Recompensa , Saciação/fisiologia , Adolescente , Regulação do Apetite/fisiologia , Estudos de Casos e Controles , Craniofaringioma/fisiopatologia , Sinais (Psicologia) , Ingestão de Energia/fisiologia , Feminino , Neuroimagem Funcional/métodos , Humanos , Masculino , Refeições/fisiologia , Obesidade/etiologia , Obesidade/fisiopatologia , Neoplasias Hipofisárias/fisiopatologia
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