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川崎病:全球负担与遗传背景

Kawasaki Disease: Global Burden and Genetic Background.

作者信息

Elakabawi Karim, Lin Jing, Jiao Fuyong, Guo Ning, Yuan Zuyi

机构信息

Cardiovascular Department, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.

Cardiovascular Department, Benha University, Benha 13518, Egypt.

出版信息

Cardiol Res. 2020 Feb;11(1):9-14. doi: 10.14740/cr993. Epub 2020 Jan 26.

Abstract

Kawasaki disease (KD) is a childhood vasculitides associated with serious coronary artery lesions. It is the most common cause of pediatric acquired heart disease in developed countries, and is increasingly reported from many rapidly industrializing developing countries. The incidence varies widely among different nations and is highest in North-East Asian countries, where almost 1 in 100 children in Japan having the disease by age of 5, where the lowest incidence reported in sub-Saharan Africa. The etiology of KD is still uncertain; interaction between a genetic predisposition and several environmental and immunological factors has been hypothesized. Several susceptibility genes were identified to be associated with the development of KD and increased risk of coronary artery lesions. Gene-gene associations and alteration of deoxyribonucleic acid (DNA) methylation are also found to play key roles in the pathogenesis and prognosis of KD. This article will focus on the global epidemiological patterns of KD, and the currently known genetic predisposition.

摘要

川崎病(KD)是一种与严重冠状动脉病变相关的儿童血管炎。它是发达国家儿童获得性心脏病的最常见病因,并且在许多快速工业化的发展中国家报告的病例越来越多。不同国家的发病率差异很大,在东北亚国家最高,日本几乎每100名5岁儿童中就有1人患病,而在撒哈拉以南非洲报告的发病率最低。KD的病因仍不确定;据推测,遗传易感性与多种环境和免疫因素之间存在相互作用。已确定有几个易感基因与KD的发生以及冠状动脉病变风险增加有关。还发现基因-基因关联和脱氧核糖核酸(DNA)甲基化改变在KD的发病机制和预后中起关键作用。本文将重点关注KD的全球流行病学模式以及目前已知的遗传易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39de/7011927/c2f446263940/cr-11-009-g001.jpg

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