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肝豆状核变性的诊疗进展与挑战

侯维 郑素军

引用本文:
Citation:

肝豆状核变性的诊疗进展与挑战

DOI: 10.12449/JCH260301
基金项目: 

国家重点研发计划 (2022YFC2304400);

北京市医院管理中心“登峰”计划专项 (DFL20241701)

利益冲突声明:本文不存在任何利益冲突。
作者贡献声明:侯维负责文献查阅,撰写初稿;郑素军负责设计论文框架和思路,指导撰写、修改文章并最后定稿。
详细信息
    通信作者:

    郑素军, zhengsujun003@126.com (ORCID: 0000-0002-8228-2819)

Advances and challenges in the diagnosis and treatment of Wilson disease

Research funding: 

National Key Research and Development Program (2022YFC2304400);

Beijing Hospitals Authority’s Ascent Plan (DFL20241701)

More Information
  • 摘要: 肝豆状核变性是一种由铜转运腺苷三磷酸酶β基因变异导致的铜代谢障碍性疾病,传统诊断主要依赖莱比锡评分,治疗则以铜螯合剂和锌制剂为主。近年来,围绕非铜蓝蛋白结合铜的多种新检测方法、肝组织金属硫蛋白免疫组化以及64Cu正电子发射断层显像-计算机体层成像等技术不断涌现,为肝豆状核变性的早期识别与病程评估提供了更多工具。同时,新剂型四盐酸曲恩汀和潜在新药甲烷氧化菌素,为安全、高效驱铜提供了新的药物选择,而基因治疗为临床治愈肝豆状核变性带来了曙光。本文系统综述了肝豆状核变性的诊断与治疗进展,讨论其在真实世界应用中的优势与局限,并对未来临床实践与研究方向提出了思考。

     

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  • 收稿日期:  2025-12-18
  • 录用日期:  2026-01-22
  • 出版日期:  2026-03-25
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