Wu Li-Na, Zhu Zhi-Jun, Sun Li-Ying
Department of Critical Liver Diseases, Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Liver Transplantation Center, National Clinical Research Center for Digestive Diseases, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Front Pediatr. 2022 Jun 29;10:912154. doi: 10.3389/fped.2022.912154. eCollection 2022.
Biliary Atresia, a common basis for neonatal cholestasis and primary indication for Liver Transplantation, accounts for 60% of pediatric Liver Transplantations. While the pathogenesis of Biliary Atresia remains obscure, abnormalities within bile ducts and the liver, inflammation, fibrosis and cilia defects are thought to comprise the pathological basis for this condition. The findings of genetic variants in Biliary Atresia, such as Copy Number Variations and Single Nucleotide Polymorphism, are considered as essential factors in the development of this condition. In this review, we summarize and analyze these Biliary Atresia variants from a perspective of their pathological characteristics. In conclusion, such analyses may offer novel insights into the pathogenesis of Biliary Atresia and provide a foundation for future studies directed toward a better understanding and treatment of Biliary Atresia.
胆道闭锁是新生儿胆汁淤积的常见病因及肝移植的主要指征,占儿童肝移植的60%。虽然胆道闭锁的发病机制尚不清楚,但胆管和肝脏内的异常、炎症、纤维化和纤毛缺陷被认为是该病的病理基础。胆道闭锁中基因变异的发现,如拷贝数变异和单核苷酸多态性,被认为是该病发生发展的重要因素。在本综述中,我们从病理特征的角度总结和分析这些胆道闭锁变异。总之,此类分析可能为胆道闭锁的发病机制提供新的见解,并为未来旨在更好地理解和治疗胆道闭锁的研究奠定基础。