Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 10 de 10
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Mol Psychiatry ; 23(8): 1737-1744, 2018 08.
Artigo em Inglês | MEDLINE | ID: mdl-29133948

RESUMO

Studies of patients with major depressive disorder (MDD) have consistently reported reduced hippocampal volumes; however, the exact pattern of these volume changes in specific anatomical subfields and their functional significance is unclear. We sought to clarify the relationship between hippocampal tail volumes and (i) a diagnosis of MDD, and (ii) clinical remission to anti-depressant medications (ADMs). Outpatients with nonpsychotic MDD (n=202) based on DSM-IV criteria and a 17-item Hamilton Rating Scale for Depression (HRSD17) score ⩾16 underwent pretreatment magnetic resonance imaging as part of the international Study to Predict Optimized Treatment for Depression (iSPOT-D). Gender-matched healthy controls (n=68) also underwent MRI scanning. An automated pipeline was used to objectively measure hippocampal subfield and whole brain volumes. Remission was defined as an HRSD17 of ⩽7 following 8 weeks of randomized open-label treatment ADMs: escitalopram, sertraline or venlafaxine-extended release. After controlling for age and total brain volume, hippocampal tail volume was larger in the MDD cohort compared to control subjects. Larger hippocampal tail volume was positively related to clinical remission, independent of total hippocampal volume, total brain volume and age. These data provide convergent evidence of the importance of the hippocampus in the development or treatment of MDD. Hippocampal tail volume is proposed as a potentially useful biomarker of sensitivity to ADM treatment.


Assuntos
Antidepressivos/uso terapêutico , Transtorno Depressivo Maior/diagnóstico por imagem , Transtorno Depressivo Maior/tratamento farmacológico , Hipocampo/diagnóstico por imagem , Adulto , Fatores Etários , Citalopram/uso terapêutico , Estudos de Coortes , Preparações de Ação Retardada , Transtorno Depressivo Maior/patologia , Transtorno Depressivo Resistente a Tratamento/diagnóstico por imagem , Transtorno Depressivo Resistente a Tratamento/tratamento farmacológico , Transtorno Depressivo Resistente a Tratamento/patologia , Feminino , Hipocampo/efeitos dos fármacos , Hipocampo/patologia , Humanos , Interpretação de Imagem Assistida por Computador , Imageamento por Ressonância Magnética , Masculino , Tamanho do Órgão , Reconhecimento Automatizado de Padrão , Prognóstico , Escalas de Graduação Psiquiátrica , Indução de Remissão , Sertralina/uso terapêutico , Cloridrato de Venlafaxina/uso terapêutico
2.
Br J Anaesth ; 118(5): 680-688, 2017 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-28510745

RESUMO

Cognitive dysfunction is a poorly understood but potentially devastating complication of cardiac surgery. Clinically meaningful assessment of cognitive changes after surgery is problematic because of the absence of a means to obtain reproducible, objective, and quantitative measures of the neural disturbances that cause altered brain function. By using both structural and functional connectivity magnetic resonance imaging data to construct a map of the inter-regional connections within the brain, connectomics has the potential to increase the specificity and sensitivity of perioperative neurological assessment, permitting rational individualized assessment and improvement of surgical techniques.


Assuntos
Lesões Encefálicas/diagnóstico por imagem , Lesões Encefálicas/psicologia , Procedimentos Cirúrgicos Cardíacos/métodos , Transtornos Cognitivos/diagnóstico por imagem , Transtornos Cognitivos/psicologia , Conectoma , Rede Nervosa/diagnóstico por imagem , Complicações Pós-Operatórias/diagnóstico por imagem , Complicações Pós-Operatórias/psicologia , Transtornos Cognitivos/etiologia , Humanos , Vias Neurais/anatomia & histologia , Vias Neurais/diagnóstico por imagem
4.
Psychol Med ; 46(10): 2157-68, 2016 07.
Artigo em Inglês | MEDLINE | ID: mdl-27192934

RESUMO

BACKGROUND: Hippocampal volume reductions in major depression have been frequently reported. However, evidence for functional abnormalities in the same region in depression has been less clear. We investigated hippocampal function in depression using functional magnetic resonance imaging (fMRI) and neuropsychological tasks tapping spatial memory function, with complementing measures of hippocampal volume and resting blood flow to aid interpretation. METHOD: A total of 20 patients with major depressive disorder (MDD) and a matched group of 20 healthy individuals participated. Participants underwent multimodal magnetic resonance imaging (MRI): fMRI during a spatial memory task, and structural MRI and resting blood flow measurements of the hippocampal region using arterial spin labelling. An offline battery of neuropsychological tests, including several measures of spatial memory, was also completed. RESULTS: The fMRI analysis showed significant group differences in bilateral anterior regions of the hippocampus. While control participants showed task-dependent differences in blood oxygen level-dependent (BOLD) signal, depressed patients did not. No group differences were detected with regard to hippocampal volume or resting blood flow. Patients showed reduced performance in several offline neuropsychological measures. All group differences were independent of differences in hippocampal volume and hippocampal blood flow. CONCLUSIONS: Functional abnormalities of the hippocampus can be observed in patients with MDD even when the volume and resting perfusion in the same region appear normal. This suggests that changes in hippocampal function can be observed independently of structural abnormalities of the hippocampus in depression.


Assuntos
Transtorno Depressivo Maior/fisiopatologia , Hipocampo/fisiopatologia , Memória Espacial/fisiologia , Adulto , Transtorno Depressivo Maior/diagnóstico por imagem , Feminino , Hipocampo/diagnóstico por imagem , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade
5.
Biol Psychol ; 106: 1-10, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25637786

RESUMO

Impaired error awareness is related to poorer outcome following traumatic brain injury (TBI). Error awareness deficits are also found in major depressive disorder (MDD), but have not been examined in the MDD that follows a TBI (TBI-MDD). This study assessed neural activity related to error awareness in TBI-MDD. Four groups completed a response inhibition task while EEG was recorded- healthy controls (N = 15), MDD-only (N = 15), TBI-only (N = 16), and TBI-MDD (N = 12). Error related EEG activity was compared using powerful randomisation statistics that included all electrodes and time points. Participants with TBI-MDD displayed less frontally distributed neural activity, suggesting reduced contribution from frontal generating sources. Neural activity during this time window is thought to reflect conscious awareness of errors. The TBI-only and MDD-only groups did not differ from controls, and early error processing was unaffected, suggesting early error detection is intact.


Assuntos
Conscientização , Lesões Encefálicas/psicologia , Depressão/psicologia , Adulto , Afeto , Idoso , Lesões Encefálicas/complicações , Estado de Consciência , Depressão/etiologia , Transtorno Depressivo Maior/fisiopatologia , Transtorno Depressivo Maior/psicologia , Manual Diagnóstico e Estatístico de Transtornos Mentais , Eletroencefalografia , Emoções , Potenciais Evocados , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estimulação Luminosa , Desempenho Psicomotor , Adulto Jovem
6.
Psychol Med ; 43(12): 2513-21, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23473554

RESUMO

BACKGROUND: Several neuroimaging studies have investigated brain grey matter in people with body dysmorphic disorder (BDD), showing possible abnormalities in the limbic system, orbitofrontal cortex, caudate nuclei and temporal lobes. This study takes these findings forward by investigating white matter properties in BDD compared with controls using diffusion tensor imaging. It was hypothesized that the BDD sample would have widespread significantly reduced white matter connectivity as characterized by fractional anisotropy (FA). METHOD: A total of 20 participants with BDD and 20 healthy controls matched on age, gender and handedness underwent diffusion tensor imaging. FA, a measure of water diffusion within a voxel, was compared between groups on a voxel-by-voxel basis across the brain using tract-based spatial statistics within the FSL package. RESULTS: Results showed that, compared with healthy controls, BDD patients demonstrated significantly lower FA (p < 0.05) in most major white matter tracts throughout the brain, including in the superior longitudinal fasciculus, inferior fronto-occipital fasciculus and corpus callosum. Lower FA levels could be accounted for by increased radial diffusivity as characterized by eigenvalues 2 and 3. No area of higher FA was found in BDD. CONCLUSIONS: This study provided the first evidence of compromised white matter integrity within BDD patients. This suggests that there are inefficient connections between different brain areas, which may explain the cognitive and emotion regulation deficits within BDD patients.


Assuntos
Transtornos Dismórficos Corporais/fisiopatologia , Encéfalo/fisiopatologia , Imagem de Tensor de Difusão/métodos , Leucoencefalopatias/fisiopatologia , Vias Neurais/fisiopatologia , Adulto , Anisotropia , Encéfalo/patologia , Imagem de Tensor de Difusão/instrumentação , Feminino , Humanos , Leucoencefalopatias/patologia , Masculino , Pessoa de Meia-Idade , Vias Neurais/patologia
7.
Int J Dev Neurosci ; 29(2): 137-43, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21147212

RESUMO

Traumatic brain injury (TBI) in children results in damage to the developing brain, particularly in severely injured individuals. Little is known, however, of the long-term structural aspects of the brain following childhood TBI. This study investigated the integrity of the brain 10 years post-TBI using magnetic resonance imaging volumetrics in a sample of 49 participants with mild, moderate and severe TBI, evaluated against a normative sample of 20 individuals from a pediatric database with comparable age and gender distribution. Structural integrity was investigated in gray and white matter, and by manually segmenting two regions of interest (hippocampus, amygdala), potentially vulnerable to the effects of childhood TBI. The results indicate that more severe injuries caused a reduction in gray and white brain matter, while all TBI severity levels resulted in increased volumes of cerebrospinal fluid and smaller hippocampal volumes. In addition, enlarged amygdala volumes were detected in severely injured patients compared to their mild and moderate counterparts, suggesting that childhood TBI may disrupt the development of certain brain regions through diffuse pathological changes. The findings highlight the lasting impact of childhood TBI on the brain and the importance of monitoring brain structure in the long-term after early injury.


Assuntos
Tonsila do Cerebelo/anatomia & histologia , Tonsila do Cerebelo/patologia , Lesões Encefálicas/patologia , Hipocampo/anatomia & histologia , Hipocampo/patologia , Adolescente , Tonsila do Cerebelo/crescimento & desenvolvimento , Atrofia/patologia , Mapeamento Encefálico/métodos , Criança , Pré-Escolar , Hipocampo/crescimento & desenvolvimento , Humanos , Lactente , Estudos Longitudinais , Imageamento por Ressonância Magnética , Masculino , Estudos Prospectivos
8.
Acta Psychiatr Scand ; 120(4): 265-73, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19486330

RESUMO

OBJECTIVE: To identify possible differences in the mean midsagittal corpus callosum (CC) total and subdivision areas in treatment-resistant schizophrenia and depression (TRS and TRD) patients. METHOD: Areas of the total CC and its five equidistant subregions (from CC1 to CC5) obtained by parallel grid partitioning schemes were manually segmented from brain MRI of 42 TRS, 45 TRD patients and 30 healthy controls. The intracranial volume (ICV) normalized areas were calculated and compared between groups. RESULTS: When compared with controls, patients with TRS had reduced ICV and a larger CC5, and TRD patients had a smaller CC4 while no significant difference in CC total area in patients with TRS or TRD was found. Multiple individual segments and total CC areas were significantly larger in TRS than TRD patients after normalization. CONCLUSION: Patients with TRS and TRD have different CC morphological characteristics, and therefore there may be aberrant interhemispheric connectivity in schizophrenia and major depressive disorder patients.


Assuntos
Agenesia do Corpo Caloso , Corpo Caloso/fisiopatologia , Transtorno Depressivo Maior/tratamento farmacológico , Transtorno Depressivo Maior/fisiopatologia , Resistência a Medicamentos , Esquizofrenia/tratamento farmacológico , Esquizofrenia/fisiopatologia , Adolescente , Adulto , Antipsicóticos/classificação , Antipsicóticos/uso terapêutico , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Adulto Jovem
9.
Aging Ment Health ; 7(4): 238-50, 2003 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12888435

RESUMO

We review nineteen empirical studies of mild cognitive impairment (MCI), age-associated memory impairment (AAMI) and related classifications reporting volumetric data on the hippocampus, entorhinal cortex and amygdala. Studies varied considerably in terms of the selection of participants, sample characteristics, the definitions of regions of interest and normalization techniques. Effect sizes for differences in left hippocampal volume and right hippocampal volumes of AAMI, MCI and pre-clinical dementia groups compared with controls ranged from 0.47 to 1.34. Effect sizes for left and right hippocampal volumes for Alzheimer's disease (AD) versus control were 1.88 and 1.75 respectively. Longitudinal results confirm that initial hippocampal volume is predictive of conversion to AD. Greater standardization in methodology and the development of normative age-referenced databases of regional brain volumes is required.


Assuntos
Transtornos Cognitivos/diagnóstico , Imageamento por Ressonância Magnética , Idoso , Envelhecimento/patologia , Doença de Alzheimer/diagnóstico , Doença de Alzheimer/fisiopatologia , Austrália , Encéfalo/anatomia & histologia , Transtornos Cognitivos/classificação , Feminino , Humanos , Masculino , Pessoa de Meia-Idade
10.
Urology ; 49(1): 2-9, 1997 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-9000177

RESUMO

Personal computers may be used to create, store, and deliver graphical presentations. With computer-generated combinations of the five media (text, images, sound, video, and animation)--that is, multimedia presentations--the effectiveness of message delivery can be greatly increased. The basic tools are (1) a personal computer; (2) presentation software; and (3) a projector to enlarge the monitor images for audience viewing. Use of this new method has grown rapidly in the business-conference world, but has yet to gain widespread acceptance at medical meetings. We review herein the rationale for multimedia presentations in medicine (vis-à-vis traditional slide shows) as an improved means for increasing audience attention, comprehension, and retention. The evolution of multimedia is traced from earliest times to the present. The steps involved in making a multimedia presentation are summarized, emphasizing advances in technology that bring the new method within practical reach of busy physicians. Specific attention is given to software, digital image processing, storage devices, and delivery methods. Our development of a urology multimedia presentation--delivered May 4, 1996, before the Society for Urology and Engineering and now Internet-accessible at http://www.usrf.org--was the impetus for this work.


Assuntos
Comunicação , Gráficos por Computador , Multimídia , Comunicação/história , História do Século XV , História do Século XIX , História do Século XX , História Antiga , História Medieval , Humanos , Multimídia/história
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...