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首页> 外文期刊>Molecular Psychiatry >Associations between prepulse inhibition and executive visual attention in children with the 22q11 deletion syndrome
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Associations between prepulse inhibition and executive visual attention in children with the 22q11 deletion syndrome

机译:22q11缺失综合征患儿的前冲抑制与执行视觉注意之间的关联

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摘要

The 22q11 deletion syndrome (DS) results in the loss of approximately 30 gene copies and is associated with possible physical anomalies, varied learning disabilities, and a specific cluster of neurocognitive deficits, including primary impairment in working memory, executive visual attention, and sensorimotor processing. Retrospective studies have suggested that children with 22q11DS are at 25 times greater risk of developing schizophrenia, thus specification of early brain network vulnerabilities among children with 22q11DS is critical. Previously, we reported that children with 22q11DS as compared with sibling controls had selective deficits in visual executive attention, and subsequently found lowered prepulse inhibition (PPI) in these same children. Visual executive attention and PPI recruit the same brain pathways linking prefrontal cortex to basal ganglia structures. To test the specificity of brain pathway vulnerability among children with 22q11DS, we examined visual executive attention and PPI paradigm data collected during the same test session from 21 children with 22q11DS and 25 sibling controls. We predicted lower %PPI and less efficient executive attention scores, and a significant inverse correlation between measures. %PPI in children with 22q11DS as compared with sibling controls was 20% lower, and visual executive attention efficiency scores 40% worse. As predicted, %PPI was inversely correlated only with executive attention efficiency scores. The implications of these findings with regard to brain pathway vulnerability in children with 22q11DS are considered. These results suggest that children with 22q11DS have early functional abnormality in pathways linking the prefrontal cortex and basal ganglia.
机译:22q11缺失综合症(DS)导致大约30个基因拷贝的丢失,并与可能的身体异常,各种学习障碍以及特定的神经认知缺陷簇有关,包括工作记忆,执行视觉注意力和感觉运动处理的主要障碍。回顾性研究表明,患有22q11DS的儿童患精神分裂症的风险高25倍,因此,确定患有22q11DS的儿童的早期脑网络脆弱性至关重要。以前,我们报道22q11DS患儿与同胞对照者相比,视觉执行者注意力存在选择性缺陷,随后发现这些患儿的前冲抑制(PPI)降低。视觉主管注意力和PPI招募了将前额叶皮层与基底神经节结构联系起来的相同大脑途径。为了测试22q11DS儿童的脑通路脆弱性的特异性,我们检查了在同一次测试期间从21名22q11DS儿童和25个同级对照中收集的视觉执行注意力和PPI范例数据。我们预测较低的%PPI和较低的执行人员注意分数,以及度量之间的显着反相关。与兄弟姐妹对照组相比,患有22q11DS的儿童的%PPI降低了20%,而视觉执行者注意效率的得分则降低了40%。如预测的那样,%PPI仅与执行者注意效率得分成反比。考虑了这些发现对22q11DS儿童脑通路脆弱性的影响。这些结果表明,患有22q11DS的儿童在连接前额叶皮层和基底神经节的途径中具有早期功能异常。

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