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1.
Cereb Cortex ; 30(7): 4238-4245, 2020 06 01.
Artigo em Inglês | MEDLINE | ID: mdl-32147718

RESUMO

Reactive attachment disorder (RAD) is associated with childhood maltreatment and affects approximately 1% of the general population. Recent data suggest that childhood maltreatment is associated with brain alterations in white and gray matter. However, the neural mechanisms of RAD-related brain alterations remain unknown. Herein, we evaluated the white matter pathways and gray matter volumes in 31 and 41 age-matched children with RAD and typical development (TD), respectively, by analyzing T1- and diffusion-weighted images. An increased fractional anisotropy (FA) and axial diffusivity in the anterior thalamic radiations (ATR) and an increased volume in the bilateral pallidum and right thalamus were observed in children with RAD compared with those with TD. Moreover, the volume of the thalamus was associated with increased ATR FA in children with RAD. Our study confirmed the existence of atypical neurodevelopment processes in the thalamus, pallidum, and ATR in children with RAD and highlighted an interdependent relationship between the alterations in the thalamus and ATR. These findings may help to improve our understanding of the comprehensive neural mechanisms of RAD.


Assuntos
Substância Cinzenta/diagnóstico por imagem , Transtorno Reativo de Vinculação na Infância/diagnóstico por imagem , Tálamo/diagnóstico por imagem , Substância Branca/diagnóstico por imagem , Adolescente , Encéfalo/diagnóstico por imagem , Encéfalo/patologia , Encéfalo/fisiopatologia , Estudos de Casos e Controles , Criança , Imagem de Tensor de Difusão , Feminino , Substância Cinzenta/patologia , Humanos , Masculino , Vias Neurais/diagnóstico por imagem , Vias Neurais/fisiopatologia , Tamanho do Órgão , Transtorno Reativo de Vinculação na Infância/fisiopatologia , Transtorno Reativo de Vinculação na Infância/psicologia , Índice de Gravidade de Doença , Tálamo/patologia , Substância Branca/patologia , Substância Branca/fisiopatologia
2.
Cortex ; 48(4): 492-503, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21074149

RESUMO

Pseudohypacusis is a somatoform disorder characterized by hearing loss with discrepancies between pure-tone audiometry and auditory brainstem response (ABR), but the underlying neuronal mechanisms remain unclear. Using voxel-based morphometry (VBM) with magnetic resonance (MR) imaging for 14 unmedicated, right-handed patients and 35 healthy control subjects, we investigated whether functional hearing loss was associated with discernible changes of brain morphology. Group differences in gray matter volume (GMV) were assessed using high-resolution, T1-weighted, volumetric MR imaging datasets (3T Trio scanner; Siemens AG) and analyzed with covariant factors of age, sex, socioeconomic status (SES), and total GMV, which was increased by 27.9% in the left medial frontal gyrus (MFG) (Brodmann area 10) (p=.001, corrected cluster level) and by 14.4% in the right superior temporal gyrus (STG) and the adjacent middle temporal gyrus (MTG) (BA42 to 21) (p=.009, corrected cluster level) in patients with pseudohypacusis. The GMV in the right STG (BA42) and verbal intelligence quotient (IQ) were correlated significantly with the Wechsler Intelligence Scale for Children - Third Edition (WISC-III) (ß=-.57, p<.0001) and level of SES (ß=-.55, p<.0001). The present findings suggest that the development of the auditory association cortex involved in language processing is affected, causing insufficient pruning during brain development. We therefore assert that differences in the neuroanatomical substrate of pseudohypacusis subjects result from a developmental disorder in auditory processing.


Assuntos
Lobo Frontal/patologia , Transtornos Somatoformes/patologia , Lobo Temporal/patologia , Estimulação Acústica , Adolescente , Agressão/fisiologia , Atenção/fisiologia , Audiometria de Tons Puros , Criança , Análise por Conglomerados , Cognição/fisiologia , Depressão/psicologia , Emoções/fisiologia , Potenciais Evocados Auditivos do Tronco Encefálico/fisiologia , Feminino , Transtornos da Audição/etiologia , Humanos , Processamento de Imagem Assistida por Computador , Testes de Inteligência , Imageamento por Ressonância Magnética , Masculino , Testes Neuropsicológicos , Escalas de Graduação Psiquiátrica , Fatores Socioeconômicos , Transtornos Somatoformes/psicologia
3.
Am J Physiol Regul Integr Comp Physiol ; 289(5): R1273-9, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-15961535

RESUMO

In recent years, circadian rhythm sleep disorders in humans have been increasing. Clinical features characteristic of this disorder are well known, but the specific causes remain unknown. However, various derangements of circadian expression of the clock gene are a probable cause of this disease. We have attempted to elucidate the relationship between the expression of the clock genes in whole blood cells and the clinical features characteristic of this disorder. In this study, we indicate the daily expression of clock genes period (Per) 1, 2, 3, Bmal1, and Clock in whole blood cells in 12 healthy male subjects. The peak phase of Per1, Per2, and Per3 appeared in the early morning, whereas that of Bmal1 and Clock appeared in the midnight hours. Furthermore, in one patient case with circadian rhythm sleep disorder, we observed variations of the peak phase in clock genes by treatments such as light therapy, exercise therapy, and medicinal therapy. This study suggested that the monitoring of human clock genes in whole blood cells, which may be functionally important for the molecular control of the circadian pacemaker as well as in suprachiasmatic nucleus, might be useful to evaluate internal synchronization.


Assuntos
Relógios Biológicos/genética , Células Sanguíneas/metabolismo , Ritmo Circadiano/genética , Expressão Gênica/fisiologia , Transtornos do Sono do Ritmo Circadiano/fisiopatologia , Fatores de Transcrição ARNTL , Adulto , Fatores de Transcrição Hélice-Alça-Hélice Básicos/genética , Fatores de Transcrição Hélice-Alça-Hélice Básicos/metabolismo , Relógios Biológicos/fisiologia , Proteínas CLOCK , Proteínas de Ciclo Celular , Ritmo Circadiano/fisiologia , Humanos , Masculino , Proteínas Nucleares/genética , Proteínas Nucleares/metabolismo , Proteínas Circadianas Period , Fatores de Tempo , Transativadores/genética , Transativadores/metabolismo , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismo
4.
No To Hattatsu ; 35(4): 331-5, 2003 Jul.
Artigo em Japonês | MEDLINE | ID: mdl-12875211

RESUMO

Two adolescents with complex regional pain syndrome (CRPS) were treated safely and effectively by spinal cord stimulation (SCS). They complained of intractable pain resistant to conservative therapies. Whereas continuous epidural anesthesia temporarily reduced pain, SCS was more effective in alleviating chronic severe pain and improving the quality of life. With careful selection of patients, SCS therapy might be recommended even in young cases.


Assuntos
Síndromes da Dor Regional Complexa/terapia , Terapia por Estimulação Elétrica , Medula Espinal/fisiopatologia , Adolescente , Adulto , Feminino , Humanos
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