Aberrant Coupling Between Resting-State Cerebral Blood Flow and Functional Connectivity in Wilson's Disease

被引:14
|
作者
Hu, Sheng [1 ]
Wu, Hongli [1 ]
Xu, ChunSheng [2 ]
Wang, Anqin [2 ]
Wang, Yi [1 ]
Shen, Tongping [1 ]
Huang, Fangliang [1 ]
Kan, Hongxing [1 ]
Li, Chuanfu [2 ]
机构
[1] Anhui Univ Chinese Med, Med Informat Engn, Hefei, Anhui, Peoples R China
[2] Anhui Univ Chinese Med, Affiliated Hosp 1, Med Imaging Ctr, Lab Digital Med Imaging, Hefei, Anhui, Peoples R China
来源
关键词
neurovascular coupling; basal ganglia; arterial spin labeling; cerebral blood flow; functional magnetic resonance imaging; NEUROLOGICAL MANIFESTATIONS; COMPENSATORY MECHANISMS; MOTOR CORTEX; BRAIN MRI; AMPLITUDE; NETWORK; ABNORMALITIES; METABOLISM; RESOLUTION; DOPAMINE;
D O I
10.3389/fncir.2019.00025
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Both abnormalities of resting-state cerebral blood flow (CBF) and functional connectivity in Wilson's disease (WD) have been identified by several studies. Whether the coupling of CBF and functional connectivity is imbalanced in WD remains largely unknown. To assess this possibility, 27 patients with WD and 27 sex- and age-matched healthy controls were recruited to acquire functional MRI and arterial spin labeling imaging data. Functional connectivity strength (FCS) and CBF were calculated based on standard gray mask. Compared to healthy controls, the CBF-FCS correlations of patients with WD were significantly decreased in the basal ganglia and the cerebellum and slightly increased in the prefrontal cortex and thalamus. In contrast, decreased CBF of patients with WD occurred predominately in subcortical and cognitive- and emotion-related brain regions, including the basal ganglia, thalamus, insular, and inferior prefrontal cortex, whereas increased CBF occurred primarily in the temporal cortex. The FCS decrease in WD patients was predominately in the basal ganglia and thalamus, and the increase was primarily in the prefrontal cortex. These findings suggest that aberrant neurovascular coupling in the brain may be a possible neuropathological mechanism underlying WD.
引用
收藏
页数:9
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