Gray matter alterations and neurotransmitter system associations in hepatitis B virus-related cirrhosis: insights into neuropathogenesis and therapeutic targets.

IF 2.4 3区 医学 Q2 CLINICAL NEUROLOGY Neuroradiology Pub Date : 2025-03-14 DOI:10.1007/s00234-025-03579-0
Lubin Gou, Junqiang Lei, Huling Ren, Yanli Zhang, Xiaoli Chen, Shuaiwen Wang, Yu Dou
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Abstract

Introduction: The associations between gray matter (GM) change and neurotransmitter systems in hepatitis B virus-related cirrhosis (HBV-RC) are still poorly understood.

Methods: We recruited 60 HBV-RC patients and 60 healthy controls (HCs). Difference of GM volume between HBV-RC and HC groups was evaluated at global and voxel levels. The potential relationship between GM morphology and prognostic models of liver function was evaluated at voxel level in HBV-RC patients. The spatial correspondence between regional GM alteration and the distribution of multiple neurotransmitter systems in HBV-RC compared to healthy controls was assessed by the JuSpace toolbox covering various neurotransmitter maps.

Results: Total GM volume in HBV-RC group was smaller than in HC group (p < 0.05), and the pattern of GM volume alterations showed significantly increased volume in bilateral thalamus and ventral diencephalon and decreased volume in bilateral basal ganglia and cerebellum (p < 0.05, FWE corrected). In HBV-RC group, the volume of left superior frontal gyrus medial segment and right middle frontal gyrus was positively correlated with serum albumin level and negatively correlated with ALBI score, and serum bilirubin level was negatively correlated with right hippocampus and caudate (p < 0.05, FWE corrected). GM alterations in HBV-RC patients relative to HCs were significantly associated with the intrinsic distribution of various neurotransmitter pathways, including GABAergic, cholinergic, serotonergic, and dopaminergic (p < 0.05).

Conclusion: The pattern of GM alteration correlated with liver function and specific neurotransmitter deficits in HBV-RC patients. These findings provide new insight into the complex neuropathogenesis of HBV-RC and the possible therapeutic targets based on neurotransmitter modulation.

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简介:乙型肝炎病毒相关性肝硬化(HBV-RC)患者的灰质(GM)变化与神经递质系统之间的关系尚不清楚:乙型肝炎病毒相关性肝硬化(HBV-RC)患者的灰质(GM)变化与神经递质系统之间的关系仍不甚明了:我们招募了 60 名 HBV-RC 患者和 60 名健康对照组(HCs)。方法:我们招募了 60 名 HBV-RC 患者和 60 名健康对照组(HCs),在整体和体素水平上评估了 HBV-RC 组和 HC 组之间 GM 体积的差异。在体素水平上评估了 HBV-RC 患者 GM 形态与肝功能预后模型之间的潜在关系。通过涵盖各种神经递质图谱的 JuSpace 工具箱,评估了与健康对照组相比,HBV-RC 患者区域 GM 改变与多种神经递质系统分布之间的空间对应关系:结果:HBV-RC 组的 GM 总体积小于 HC 组(p 结论:HBV-RC 组的 GM 总体积小于 HC 组(p 结论):HBV-RC患者的基因组改变模式与肝功能和特定神经递质缺陷相关。这些发现为了解 HBV-RC 复杂的神经发病机制以及基于神经递质调节的可能治疗靶点提供了新的视角。
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来源期刊
Neuroradiology
Neuroradiology 医学-核医学
CiteScore
5.30
自引率
3.60%
发文量
214
审稿时长
4-8 weeks
期刊介绍: Neuroradiology aims to provide state-of-the-art medical and scientific information in the fields of Neuroradiology, Neurosciences, Neurology, Psychiatry, Neurosurgery, and related medical specialities. Neuroradiology as the official Journal of the European Society of Neuroradiology receives submissions from all parts of the world and publishes peer-reviewed original research, comprehensive reviews, educational papers, opinion papers, and short reports on exceptional clinical observations and new technical developments in the field of Neuroimaging and Neurointervention. The journal has subsections for Diagnostic and Interventional Neuroradiology, Advanced Neuroimaging, Paediatric Neuroradiology, Head-Neck-ENT Radiology, Spine Neuroradiology, and for submissions from Japan. Neuroradiology aims to provide new knowledge about and insights into the function and pathology of the human nervous system that may help to better diagnose and treat nervous system diseases. Neuroradiology is a member of the Committee on Publication Ethics (COPE) and follows the COPE core practices. Neuroradiology prefers articles that are free of bias, self-critical regarding limitations, transparent and clear in describing study participants, methods, and statistics, and short in presenting results. Before peer-review all submissions are automatically checked by iThenticate to assess for potential overlap in prior publication.
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