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SORL1基因对健康年轻成年人功能连接密度的调节作用。

Modulation effect of the SORL1 gene on functional connectivity density in healthy young adults.

作者信息

Shen Junlin, Zhang Peng, Liu Huaigui, Xu Lixue, Xu Jiayuan, Qin Wen, Liu Bing, Jiang Tianzi, Yu Chunshui

机构信息

Department of Radiology, Tianjin Medical University General Hospital, No. 154, Anshan Road, Heping District, Tianjin, 300052, China.

Brainnetome Center, Institute of Automation, Chinese Academy of Sciences, Beijing, China.

出版信息

Brain Struct Funct. 2016 Nov;221(8):4103-4110. doi: 10.1007/s00429-015-1149-x. Epub 2015 Dec 1.

Abstract

The sortilin-related receptor 1 (SORL1) gene has been associated with late-onset Alzheimer's disease (LOAD) and structural impairments in several ethnic populations. However, how this gene affects brain function properties remains unclear. We investigated associations of SORL1 rs2070045 with functional connectivity density (FCD) in healthy young adults. This single-nucleotide polymorphism was selected because it is the SORL1 variant that has been frequently associated with LOAD in several populations, including the Chinese Han population. A total of 275 healthy young Chinese Han subjects with successful genotyping and MRI examinations were included. The effect of SORL1 rs2070045 was explored using a voxel-wise FCD analysis. A significant effect of SORL1 rs2070045 on the FCD was found in the right inferior temporal gyrus. The risk G allele carriers of the rs2070045 exhibited a lower FCD than the protective TT carriers. This effect was independent of the status of apolipoprotein E. This study provides the first evidence that the SORL1 gene is associated with brain FCD differences in healthy young adults. In the genetic risk subjects, connectivity impairment already starts during young adulthood, which may predispose the risk allele carriers to be susceptible to LOAD after several decades.

摘要

sortilin相关受体1(SORL1)基因已在多个种族人群中与晚发性阿尔茨海默病(LOAD)及结构损伤相关联。然而,该基因如何影响脑功能特性仍不清楚。我们研究了SORL1 rs2070045与健康年轻成年人功能连接密度(FCD)之间的关联。选择这个单核苷酸多态性是因为它是在包括中国汉族人群在内的多个群体中经常与LOAD相关联的SORL1变体。总共纳入了275名成功进行基因分型和MRI检查的健康年轻中国汉族受试者。使用基于体素的FCD分析探究SORL1 rs2070045的作用。发现SORL1 rs2070045对右侧颞下回的FCD有显著影响。rs2070045的风险G等位基因携带者的FCD低于保护性TT携带者。这种影响独立于载脂蛋白E的状态。本研究首次提供证据表明SORL1基因与健康年轻成年人的脑FCD差异相关。在遗传风险受试者中,连接性损伤在成年早期就已开始,这可能使风险等位基因携带者在几十年后易患LOAD。

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