原发性胆汁性胆管炎合并脂质代谢异常的研究进展
DOI: 10.12449/JCH240125
利益冲突声明:本文不存在任何利益冲突。
作者贡献声明:袁诗雨负责起草文章,对行文的思路和设计有关键贡献;杨焕焕、唐映梅参与了修改文章关键内容。
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摘要: 原发性胆汁性胆管炎(PBC)是一种以肝内中小胆管进行性、非化脓性炎症为特征的自身免疫性肝病。近期研究发现PBC患者中脂质代谢异常较为常见,76%的PBC患者常合并血脂异常,其作用及危害备受关注。脂质代谢紊乱在PBC发展中起重要作用,本文主要从脂质代谢紊乱在PBC中的表现及作用、诊断及治疗方面的研究进展展开综述,以期为PBC治疗提供新的思路。Abstract: Primary biliary cholangitis (PBC) is an autoimmune liver disease characterized by progressive and non-purulent inflammation of small- and medium-sized bile ducts in the liver. Recent studies have shown that abnormal lipid metabolism is relatively common in patients with PBC, and 76% of PBC patients have dyslipidemia. The effects and harms of dyslipidemia have attracted much attention. Lipid metabolism disorders play an important role in the progression of PBC. This article mainly reviews the research advances in the manifestation, role, diagnosis, and treatment of lipid metabolism disorders in PBC, so as to provide new ideas for the treatment of PBC.
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Key words:
- Primary Biliary Cholangitis /
- Lipid Metabolism Disorders /
- Inflammation
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