Spatial working memory in neurofibromatosis 1: Altered neural activity and functional connectivity.
Spatial working memory in neurofibromatosis 1: Altered neural activity and functional connectivity.
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DOI:
10.1016/j.nicl.2017.06.032
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发表时间:
2017
期刊:
影响因子:
--
通讯作者:
Bearden CE
中科院分区:
文献类型:
--
作者:
Ibrahim AFA;Montojo CA;Haut KM;Karlsgodt KH;Hansen L;Congdon E;Rosser T;Bilder RM;Silva AJ;Bearden CE
Neurofibromatosis Type 1 (NF1) is a genetic disorder that disrupts central nervous system development and neuronal function. Cognitively, NF1 is characterized by difficulties with executive control and visuospatial abilities. Little is known about the neural substrates underlying these deficits. The current study utilized Blood-Oxygen-Level-Dependent (BOLD) functional MRI (fMRI) to explore the neural correlates of spatial working memory (WM) deficits in patients with NF1. BOLD images were acquired from 23 adults with NF1 (age M = 32.69; 61% male) and 25 matched healthy controls (age M = 33.08; 64% male) during an in-scanner visuo-spatial WM task. Whole brain functional and psycho-physiological interaction analyses were utilized to investigate neural activity and functional connectivity, respectively, during visuo-spatial WM performance. Participants also completed behavioral measures of spatial reasoning and verbal WM. Relative to healthy controls, participants with NF1 showed reduced recruitment of key components of WM circuitry, the left dorsolateral prefrontal cortex and right parietal cortex. In addition, healthy controls exhibited greater simultaneous deactivation between the posterior cingulate cortex (PCC) and temporal regions than NF1 patients. In contrast, NF1 patients showed greater PCC and bilateral parietal connectivity with visual cortices as well as between the PCC and the cerebellum. In NF1 participants, increased functional coupling of the PCC with frontal and parietal regions was associated with better spatial reasoning and WM performance, respectively; these relationships were not observed in controls. Dysfunctional engagement of WM circuitry, and aberrant functional connectivity of ‘task-negative’ regions in NF1 patients may underlie spatial WM difficulties characteristic of the disorder. NF1 is a monogenic disorder associated with executive function deficits. Hypoactivity of working memory circuitry in NF1 patients relative to controls Increased PCC connectivity with visual cortex/cerebellum in NF1 patients during task Greater simultaneous deactivation between default mode regions in controls Greater PCC-frontal coupling associated with better behavioral performance in NF1
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