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  • Wiley  (2)
  • Qi, Rongfeng  (2)
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  • Wiley  (2)
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  • 1
    In: Brain and Behavior, Wiley, Vol. 11, No. 1 ( 2021-01)
    Abstract: New evidence suggests that the centromedial amygdala (CMA) and the basolateral amygdala (BLA) play different roles in threat processing. Our study aimed to investigate the effects of trauma and post‐traumatic stress disorder (PTSD) on the functional connectivity (FC) of the amygdala and its subregions. Methods Twenty‐seven patients with typhoon‐related PTSD, 33 trauma‐exposed controls (TEC), and 30 healthy controls (HC) were scanned with a 3‐Tesla magnetic resonance imaging scanner. The FCs of the BLA, the CMA, and the amygdala as a whole were examined using a seed‐based approach, and then, the analysis of variance was used to compare the groups. Results We demonstrated that the BLA had a stronger connectivity with the prefrontal cortices (PFCs) and angular gyrus in the PTSD group than in the TEC group. Additionally, compared with the PTSD and the HC groups, the TEC group exhibited decreased and increased BLA FC with the ventromedial PFC and postcentral gyrus (PoCG), respectively. Furthermore, the PTSD group showed abnormal FC between the salience network and default‐mode network, as well as the executive control network. Compared with the HC group, the TEC group and the PTSD group both showed decreased BLA FC with the superior temporal gyrus (STG). Finally, the FCs between the bilateral amygdala (as a whole) and the vmPFC, and between the BLA and the vmPFC have a negative correlation with the severity of PTSD. Conclusions Decreased BLA‐vmPFC FC and increased BLA‐PoCG FC may reflect PTSD resilience factors. Trauma leads to decreased connectivity between the BLA and the STG, which could be further aggravated by PTSD.
    Type of Medium: Online Resource
    ISSN: 2162-3279 , 2162-3279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2623587-0
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  • 2
    In: Journal of Magnetic Resonance Imaging, Wiley
    Abstract: Patients with hepatitis B virus‐related cirrhosis (HBV‐RC) exhibit progressive neurologic dysfunction from primary sensorimotor to high‐order cognition, as their disease advances. However, the exact neurobiologic mechanisms and the potential association with gene‐expression profiles are not fully understood. Purpose To explore the hierarchical disorganization in the large‐scale functional connectomes in HBV‐RC patients and to investigate its potential underlying molecular basis. Study Type Prospective. Population Fifty HBV‐RC patients and 40 controls (Cohort 1) and 30 HBV‐RC patients and 38 controls (Cohort 2). Field Strength/Sequence Gradient‐echo echo‐planar and fast field echo sequences at 3.0 T (Cohort 1) and 1.5 T (Cohort 2). Assessment Data were processed with Dpabi and the BrainSpace package. Gradient scores were evaluated from global to voxel level. Cognitive measurement and patients grouping were based on psychometric hepatic encephalopathy scores. The whole‐brain microarray‐based gene‐expression data were obtained from the AIBS website. Statistical Tests One‐way ANOVA, chi‐square test, two‐sample t ‐test, Kruskal–Wallis test, Spearman's correlation coefficient ( r ), the gaussian random field correction, false discovery rate (FDR) correction and the Bonferroni correction. Significance level: P   〈  0.05. Results HBV‐RC patients exhibited a robust and replicable connectome gradient dysfunction, which was significantly associated with the gene‐expression profiles in both cohorts ( r  = 0.52 and r  = 0.56, respectively). The most correlated genes were enriched in γ‐aminobutyric acid (GABA) and GABA‐related receptor genes (FDR q value 〈 0.05). Moreover, the connectome gradient dysfunction at network level observed in HBV‐RC patients correlated with their poor cognitive performance (Cohort 2: visual network, r  = −0.56; subcortical network, r  = 0.66; frontoparietal network, r  = 0.51). Data Conclusion HBV‐RC patients had hierarchical disorganization in the large‐scale functional connectomes, which may underly their cognitive impairment. In addition, we showed the potential molecular mechanism of the connectome gradient dysfunction, which suggested the importance of GABA and GABA‐related receptor genes. Evidence Level 2 Technical Efficacy Stage 2
    Type of Medium: Online Resource
    ISSN: 1053-1807 , 1522-2586
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 1497154-9
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