首页|基于铜代谢的肝豆状核变性相关分子机制的研究进展

基于铜代谢的肝豆状核变性相关分子机制的研究进展

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肝豆状核变性[又称威尔逊病(Wilson disease,WD)]是一种常染色体隐性遗传性铜代谢障碍疾病,其临床表现主要包括肝脏损伤、神经功能障碍和精神疾病.WD的机制尚不完全清楚,目前普遍认为铜蓄积是其主要原因,但近年来铜死亡的发现以及锌、铁、铅对铜代谢的影响也引起了关注,并已有相关研究.因此本文在分子层面上对WD的肝损伤和神经精神性疾病的过程、影响因素、发病症状等作出整理,为WD患者提供可选择性的新治疗手段,为临床诊断提供可参考的靶点和方法.
Progress in molecular pathological mechanisms of Wilson disease based on copper metabolism abnormality
Hepatolenticular degeneration,also known as Wilson disease(WD),is a kind of autosomal reces-sive hereditary disease with the disorder of copper metabolism,which is clinically manifested as liver damage,neuropsy-chiatric disorder.The molecular pathological mechanism has been not fully revealed.It is commonly known that excessive copper accumulation inside hepatotic cells is the main reason of WD.However,the emerging roles of cuproptosis and oth-er trace elements such as zinc,iron and lead in WD have recently attracted attention and become the research hotspots.This present review summarized the pathological factors,molecular mechanisms of liver damage and neuropsychiatric dis-order of WD,which will help identify novel diagnostic biomarkers,and provide new therapeutics for WD.

hepatolenticular degenerationcopper metabolismATP7B gene

李金贤、温鼎声、李雄

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广东药科大学附属第一医院临床药学重点专科,广东 广州 510000

肝豆状核变性 铜代谢 ATP7B基因

广东省医学科研基金资助项目广东省医院药师青年托举研究基金(晴粤药学基金)资助项目中央财政医疗服务与保障能力提升资金资助项目

B20212432023QNTJ36Z155080000004

2024

中国病理生理杂志
中国病理生理学会

中国病理生理杂志

CSTPCD北大核心
影响因子:1.065
ISSN:1000-4718
年,卷(期):2024.40(9)