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1.
Ann Rheum Dis ; 77(8): 1107-1117, 2018 08.
Artigo em Inglês | MEDLINE | ID: mdl-29592918

RESUMO

BACKGROUND: In 2012, a European initiative called Single Hub and Access point for pediatric Rheumatology in Europe (SHARE) was launched to optimise and disseminate diagnostic and management regimens in Europe for children and young adults with rheumatic diseases. Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in children and uveitis is possibly its most devastating extra-articular manifestation. Evidence-based guidelines are sparse and management is mostly based on physicians' experience. Consequently, treatment practices differ widely, within and between nations. OBJECTIVES: To provide recommendations for the diagnosis and treatment of JIA-associated uveitis. METHODS: Recommendations were developed by an evidence-informed consensus process using the European League Against Rheumatism standard operating procedures. A committee was constituted, consisting of nine experienced paediatric rheumatologists and three experts in ophthalmology from Europe. Recommendations derived from a validated systematic literature review were evaluated by an Expert Committee and subsequently discussed at two consensus meetings using nominal group techniques. Recommendations were accepted if >80% agreement was reached (including all three ophthalmologists). RESULTS: In total, 22 recommendations were accepted (with >80% agreement among experts): 3 on diagnosis, 5 on disease activity measurements, 12 on treatment and 2 on future recommendations. CONCLUSIONS: The SHARE initiative aims to identify best practices for treatment of patients suffering from JIA-associated uveitis. Within this remit, recommendations for the diagnosis and treatment of JIA-associated uveitis have been formulated by an evidence-informed consensus process to suggest a standard of care for JIA-associated uveitis patients throughout Europe.


Assuntos
Artrite Juvenil/complicações , Uveíte/etiologia , Uveíte/terapia , Antirreumáticos/uso terapêutico , Artrite Juvenil/tratamento farmacológico , Gerenciamento Clínico , Medicina Baseada em Evidências/métodos , Glucocorticoides/uso terapêutico , Humanos , Programas de Rastreamento/métodos , Metotrexato/uso terapêutico , Índice de Gravidade de Doença , Uveíte/diagnóstico
2.
PLoS Biol ; 15(5): e2001421, 2017 05.
Artigo em Inglês | MEDLINE | ID: mdl-28542195

RESUMO

Information processing in neural networks depends on the connectivity among excitatory and inhibitory neurons. The presence of parallel, distinctly controlled local circuits within a cortical network may ensure an effective and dynamic regulation of microcircuit function. By applying a combination of optogenetics, electrophysiological recordings, and high resolution microscopic techniques, we uncovered the organizing principles of synaptic communication between principal neurons and basket cells in the basal nucleus of the amygdala. In this cortical structure, known to be critical for emotional memory formation, we revealed the presence of 2 parallel basket cell networks expressing either parvalbumin or cholecystokinin. While the 2 basket cell types are mutually interconnected within their own category via synapses and gap junctions, they avoid innervating each other, but form synaptic contacts with axo-axonic cells. Importantly, both basket cell types have the similar potency to control principal neuron spiking, but they receive excitatory input from principal neurons with entirely diverse features. This distinct feedback synaptic excitation enables a markedly different recruitment of the 2 basket cell types upon the activation of local principal neurons. Our data suggest fundamentally different functions for the 2 parallel basket cell networks in circuit operations in the amygdala.


Assuntos
Tonsila do Cerebelo/fisiologia , Axônios/fisiologia , Neurônios GABAérgicos/fisiologia , Interneurônios/fisiologia , Rede Nervosa/fisiologia , Proteínas do Tecido Nervoso/metabolismo , Recrutamento Neurofisiológico , Tonsila do Cerebelo/citologia , Animais , Biomarcadores/metabolismo , Mapeamento Encefálico , Quimiocinas CC/genética , Quimiocinas CC/metabolismo , Feminino , Neurônios GABAérgicos/citologia , Proteínas de Fluorescência Verde/genética , Proteínas de Fluorescência Verde/metabolismo , Interneurônios/citologia , Proteínas Luminescentes/genética , Proteínas Luminescentes/metabolismo , Masculino , Camundongos Transgênicos , Rede Nervosa/citologia , Proteínas do Tecido Nervoso/genética , Condução Nervosa , Optogenética , Parvalbuminas/genética , Parvalbuminas/metabolismo , Regiões Promotoras Genéticas/genética , Proteínas Recombinantes/metabolismo , Análise de Célula Única
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