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腭心面综合征(22q11.2缺失综合征)中非空间工作记忆的神经关联

The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome).

作者信息

Kates Wendy R, Krauss Beth R, Abdulsabur Nuria, Colgan Deirdre, Antshel Kevin M, Higgins Anne Marie, Shprintzen Robert J

机构信息

Department of Psychiatry and Behavioral Sciences, State University of New York Upstate Medical University, Syracuse, New York, USA.

出版信息

Neuropsychologia. 2007 Sep 20;45(12):2863-73. doi: 10.1016/j.neuropsychologia.2007.05.007. Epub 2007 May 24.

Abstract

Velocardiofacial syndrome (VCFS), also known as 22q11.2 deletion syndrome, is a neurogenetic disorder that is associated with both learning disabilities and a consistent neuropsychological phenotype, including deficits in executive function, visuospatial perception, and working memory. Anatomic imaging studies have identified significant volumetric reductions in the parietal lobe of individuals with VCFS, but several studies have reported that the frontal lobe is relatively preserved. We used functional magnetic resonance imaging to investigate the neural correlates of non-spatial working memory in 17 youths with VCFS, 10 of their unaffected siblings, and 10 community controls (with the same proportion of learning disabilities as the VCFS youths). Task performance of siblings tended to be more accurate than children with VCFS, who did not differ from community controls. All three-study groups recruited parietal regions that were equivalent in location and magnitude. Whereas the sibling group also recruited the dorsolateral prefrontal cortex (DLPFC), Broca's area, and anterior cingulate, DLPFC activation was absent in the whole brain analyses of children with VCFS and controls. Moreover, the magnitude of frontal activation in VCFS participants was restricted relative to both siblings and controls. These findings suggest that VCFS participants exhibit frontal hypoactivation that is not attributable to performance. In addition, VCFS children and controls (many with idiopathic learning disabilities) appear to rely on phonological rehearsal to hold information on line instead of the DLPFC. Despite previous anatomic MRI reports of preserved frontal lobe volumes in VCFS therefore, these fMRI findings suggest that the frontal component of the distributed network subserving executive function and working memory may be disrupted in youth with this disorder.

摘要

心脏颜面综合征(VCFS),也称为22q11.2缺失综合征,是一种神经遗传性疾病,与学习障碍和一致的神经心理学表型相关,包括执行功能、视觉空间感知和工作记忆方面的缺陷。解剖影像学研究发现,VCFS患者的顶叶体积显著减小,但多项研究报告称额叶相对保留。我们使用功能磁共振成像来研究17名患有VCFS的青少年、10名未受影响的兄弟姐妹以及10名社区对照者(学习障碍比例与患有VCFS的青少年相同)非空间工作记忆的神经相关性。兄弟姐妹的任务表现往往比患有VCFS的儿童更准确,而患有VCFS的儿童与社区对照者没有差异。所有三个研究组招募的顶叶区域在位置和大小上相当。虽然兄弟姐妹组还招募了背外侧前额叶皮层(DLPFC)、布洛卡区和前扣带回,但在对患有VCFS的儿童和对照者的全脑分析中未发现DLPFC激活。此外,与兄弟姐妹和对照者相比,VCFS参与者额叶激活的程度受到限制。这些发现表明,VCFS参与者表现出与表现无关的额叶激活不足。此外,患有VCFS的儿童和对照者(许多患有特发性学习障碍)似乎依赖语音复述来在线保留信息,而不是依赖DLPFC。因此,尽管之前有解剖MRI报告称VCFS患者的额叶体积保留,但这些功能磁共振成像结果表明,在患有这种疾病的青少年中,支持执行功能和工作记忆的分布式网络的额叶部分可能受到破坏。

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