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在中国人群中,HTRA1基因变异会增加患新生血管性年龄相关性黄斑变性的风险。

HTRA1 variant increases risk to neovascular age-related macular degeneration in Chinese population.

作者信息

Lu Fang, Hu Jianbin, Zhao Peiquan, Lin Ying, Yang Yang, Liu Xiaoqi, Fan Yingchuan, Chen Bin, Liao Shihuang, Du Qiong, Lei Chuntao, Cameron D Joshua, Zhang Kang, Yang Zhenglin

机构信息

Human Molecular Biology & Genetics, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Sichuan 610072, China.

出版信息

Vision Res. 2007 Nov;47(24):3120-3. doi: 10.1016/j.visres.2007.08.010. Epub 2007 Sep 27.

Abstract

Age-related macular degeneration (AMD) is a leading cause of irreversible visual impairment in the world. Advanced AMD can be divided into wet AMD (choroidal neovascularization) and dry AMD (geographic atrophy, GA). Drusen is characterized by deposits in the macula without visual loss and is an early AMD sign in the Caucasian population. rs11200638 in the promoter of HTRA1 has recently been shown to increases the risk for wet AMD in both Caucasian and Hong Kong Chinese populations. In order to replicate these results in a different cohort, we genotyped rs11200638 for 164 Chinese patients (90 wet AMD and 74 drusen) and 106 normal controls in a Han Mainland Chinese cohort. The genotypes were compared using chi square analysis for an additive allelic model. rs11200638 was significantly associated with wet AMD (p=5.00x10(-12)). Unlike in the Caucasian population, the risk allele of rs11200638 was not associated with drusen in our Chinese population. These findings confirm the association of HTRA1 with wet AMD.

摘要

年龄相关性黄斑变性(AMD)是全球不可逆视力损害的主要原因。晚期AMD可分为湿性AMD(脉络膜新生血管)和干性AMD(地图样萎缩,GA)。玻璃膜疣的特征是黄斑区有沉积物但无视力丧失,是白种人群中早期AMD的迹象。最近研究表明,HTRA1启动子中的rs11200638增加了白种人和中国香港人群患湿性AMD的风险。为了在不同队列中重复这些结果,我们在中国内地汉族队列中对164例中国患者(90例湿性AMD和74例玻璃膜疣患者)和106例正常对照进行了rs11200638基因分型。使用卡方分析对加性等位基因模型的基因型进行比较。rs11200638与湿性AMD显著相关(p=5.00x10(-12))。与白种人群不同,在我们的中国人群中,rs11200638的风险等位基因与玻璃膜疣无关。这些发现证实了HTRA1与湿性AMD的关联。

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