Abstract

Background and Aims: Liver cirrhosis commonly induces brain structural impairments that are associated with neurological complications (e.g., minimal hepatic encephalopathy (MHE)), but the topological characteristics of the brain structural network are still less well understood in cirrhotic patients with MHE. This study aimed to conduct the first investigation on the topological alterations of brain structural covariance networks in MHE.Methods: This study included 22 healthy controls (HCs) and 22 cirrhotic patients with MHE. We calculated the gray matter volume of 90 brain regions using an automated anatomical labeling (AAL) template, followed by construction of gray matter structural covariance networks by thresholding interregional structural correlation matrices as well as graph theoretical analysis.Results: MHE patients showed abnormal small-world properties of the brain structural covariance network, i.e., decreased clustering coefficient and characteristic path length and lower small-worldness parameters, which indicated a tendency toward more random architecture. In addition, MHE patients lost hubs in the prefrontal and parietal regions, although they had new hubs in the temporal and occipital regions. Compared to HC, MHE patients had decreased regional degree/betweenness involving several regions, primarily the prefrontal and parietal lobes, motor region, insula and thalamus. In addition, the MHE group also showed increased degree/betweenness in the occipital lobe and hippocampus.Conclusion: These results suggest that MHE leads to altered coordination patterns of gray matter morphology and provide structural evidence supporting the idea that MHE is a neurological complication related to disrupted neural networks.

Highlights

  • Previous studies have shown that brain structural abnormalities commonly occur in cirrhotic patients

  • functional data analysis (FDA) analysis indicated that Minimal hepatic encephalopathy (MHE) patients had significantly lower γ (P = 0.021), λ (P = 0.010) and σ (P = 0.048)

  • For the non-normalized network measures, FDA analysis indicated that the MHE group had decreased clustering coefficient (Cp) (P = 0.030) and characteristic path length (Lp) (P = 0.043), as compared with healthy controls (HCs) group

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Summary

Introduction

Previous studies have shown that brain structural abnormalities commonly occur in cirrhotic patients. Neuropathological studies have documented the loss of brain parenchyma due to cirrhosis (Kril and Butterworth, 1997). Among patients with hepatic dysfunction, neuronal cell loss (probably due to chronic portosystemic shunting and ammonia exposure) has been associated with liver failure (Butterworth, 2007). A previous study has suggested that structural alterations are associated with lower psychometric performance of cirrhotic patients (Amodio et al, 2003). Liver cirrhosis commonly induces brain structural impairments that are associated with neurological complications (e.g., minimal hepatic encephalopathy (MHE)), but the topological characteristics of the brain structural network are still less well understood in cirrhotic patients with MHE.

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