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NeuroImage. Clinical · Jan 2019
Resting-state functional connectivity predicts individual language impairment of patients with left hemispheric gliomas involving language network.
- Binke Yuan, Nan Zhang, Jing Yan, Jingliang Cheng, Junfeng Lu, and Jinsong Wu.
- Center for Language and Brain, Shenzhen Institute of Neuroscience, Shenzhen, China.
- Neuroimage Clin. 2019 Jan 1; 24: 102023.
AbstractLanguage deficits following brain tumors should consider the dynamic interactions between different tumor growth kinetics and functional network reorganization. We measured the resting-state functional connectivity of 126 patients with left cerebral gliomas involving language network areas, including 77 patients with low-grade gliomas (LGG) and 49 patients with high-grade gliomas (HGG). Functional network mapping for language was performed by construction of a multivariate machine learning-based prediction model of individual aphasia quotient (AQ), a summary score that indicates overall severity of language impairment. We found that the AQ scores for HGG patients were significantly lower than those of LGG patients. The prediction accuracy of HGG patients (R2 = 0.27, permutation P = 0.007) was much higher than that of LGG patients (R2 = 0.09, permutation P = 0.032). The rsFC regions predictive of LGG's AQ involved the bilateral frontal, temporal, and parietal lobes, subcortical regions, and bilateral cerebro-cerebellar connections, mainly in regions belonging to the canonical language network. The functional network of language processing for HGG patients showed strong dependence on connections of the left cerebro-cerebellar connections, limbic system, and the temporal, occipital, and prefrontal lobes. Together, our findings suggested that individual language processing of glioma patients links large-scale, bilateral, cortico-subcortical, and cerebro-cerebellar functional networks with different network reorganizational mechanisms underlying the different levels of language impairments in LGG and HGG patients.Copyright © 2019 The Author(s). Published by Elsevier Inc. All rights reserved.
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