首页> 外文期刊>Journal of the American Academy of Child and Adolescent Psychiatry >Early expression of a pathophysiological feature of schizophrenia: saccadic intrusions into smooth-pursuit eye movements in school-age children vulnerable to schizophrenia.
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Early expression of a pathophysiological feature of schizophrenia: saccadic intrusions into smooth-pursuit eye movements in school-age children vulnerable to schizophrenia.

机译:精神分裂症的病理生理特征的早期表达:在易患精神分裂症的学龄儿童中,有眼泪侵入了追求平滑的眼球运动。

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OBJECTIVE: Neurodevelopmental hypotheses of schizophrenia propose that the responsible pathology occurs much earlier than the usual onset of illness in late adolescence. Nonspecific neurocognitive and behavioral deficits found in children vulnerable to schizophrenia support this hypothesis. This report describes early deficits in a putative genetic endophenotype, saccadic intrusions into smooth-pursuit eye movements (SPEM). METHOD: SPEM were recorded in 189 children aged 6-15 years: 49 children with schizophrenia, 60 nonpsychotic first-degree relatives, and 80 typically developing children. RESULTS: Children with schizophrenia demonstrated poorer gain and a significantly increased frequency of leading saccades and large anticipatory saccades; however, only leading saccades differentiated first-degree relatives from typical children. Admixture analysis indicates that 94% of children with schizophrenia, 50% of first-degree relatives, and 19% of typically developing children have abnormally increased frequencies of leading saccades. CONCLUSIONS: Typically developing young school-age children have a leading saccade phenotype similar to that of adults, suggesting this brain function is fully developed by early school-age years. The abnormal leading saccade phenotype, a schizophrenia-associated familial brain dysfunction, is present by 6 years of age, more than a decade before the highest risk for onset of psychosis. Treatment and prevention strategies will need to consider the early neurodevelopmental nature of schizophrenia.
机译:目的:精神分裂症的神经发育假说提出,负责任的病理发生比青春期晚期通常的发病要早得多。在易患精神分裂症的儿童中发现的非特异性神经认知和行为缺陷支持了这一假设。该报告描述了推定的遗传内表型的早期缺陷,顺行追求眼球运动(SPEM)的acc门侵犯。方法:对189例6-15岁的儿童进行SPEM记录:49例精神分裂症儿童,60例非精神病性一级亲属和80例典型的发育中儿童。结果:精神分裂症儿童表现出较差的增益,前导扫视和大预期扫视的频率显着增加。但是,只有领导才能将一级亲属与典型儿童区分开。混合分析表明,94%的精神分裂症儿童,50%的一级亲属和19%的典型发育中儿童的前扫视频率异常增加。结论:典型的发展中的学龄儿童的前瞻性扫视表型与成人相似,表明这种大脑功能在学龄早期就已完全发育。异常的前导扫视表型是一种精神分裂症相关的家族性脑功能障碍,发病年龄为6岁,比精神病发作的最高风险还早十多年。治疗和预防策略将需要考虑精神分裂症的早期神经发育性质。

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