Suppr超能文献

遗传因素及其在胆道闭锁发病机制中的作用

Genetic Factors and Their Role in the Pathogenesis of Biliary Atresia.

作者信息

Wu Li-Na, Zhu Zhi-Jun, Sun Li-Ying

机构信息

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.

出版信息

Front Pediatr. 2022 Jun 29;10:912154. doi: 10.3389/fped.2022.912154. eCollection 2022.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b45/9277099/5e1bae3f57fa/fped-10-912154-g0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验