Modulation of APOE and SORL1 genes on hippocampal functional connectivity in healthy young adults
Shen, Junlin1,2; Qin, Wen1,2; Xu, Qiang1,2; Xu, Lixue1,2; Xu, Jiayuan1,2; Zhang, Peng1,2; Liu, Huaigui1,2; Liu, Bing3; Jiang, Tianzi3; Yu, Chunshui1,2
刊名BRAIN STRUCTURE & FUNCTION
2017-08-01
卷号222期号:6页码:2877-2889
关键词Apoe Sorl1 Hippocampus Functional Connectivity Fmri Snps
DOI10.1007/s00429-017-1377-3
文献子类Article
英文摘要Apolipoprotein E (APOE) and sortilin-related receptor (SORL1) genes act on the same metabolic pathway and have been associated with Alzheimer's disease (AD) characterized by hippocampal impairment. Although the effects of APOE on hippocampal resting-state functional connectivity (rsFC) have been reported, the main effects of SORL1 and SORL1 x APOE interactions on hippocampal rsFC in healthy subjects remain largely unknown. Here, we systematically investigated the main effects of SORL1 rs2070045, and APOE, and their interaction effects on hippocampal rsFC in healthy young adults. The main effect of APOE showed that risk epsilon 4 carriers had decreased positive hippocampal rsFC with the precuneus/posterior cingulate cortex and subgenual anterior cingulate cortex, and increased positive hippocampal rsFC with the sensorimotor cortex compared with non-epsilon 4 carriers. The main effect of SORL1 showed that risk G-allele carriers had decreased positive rsFC between the hippocampus and middle temporal gyrus compared with TT carriers. No significant additive interaction was observed. Instead, significant SORL1 x APOE non-additive interaction was found in negative rsFC between the hippocampus and inferior frontal gyrus. Compared with subjects with TT genotype, SORL1 G-allele carriers had a stronger negative rsFC in APOE epsilon 4 carriers, but a weaker negative rsFC in APOE non-epsilon 4 carriers. These findings suggest that SORL1 and APOE genes modulate different hippocampal rsFCs and have a complex interaction. The SORL1- and APOE-dependent hippocampal connectivity changes may at least partly account for their association with AD.
WOS关键词APOLIPOPROTEIN-E EPSILON-4 ; MILD COGNITIVE IMPAIRMENT ; RESTING-STATE FMRI ; EARLY ALZHEIMERS-DISEASE ; CEREBROSPINAL-FLUID ; E GENOTYPES ; MEMORY ; BRAIN ; CARRIERS ; VOLUME
WOS研究方向Anatomy & Morphology ; Neurosciences & Neurology
语种英语
WOS记录号WOS:000406778700026
资助机构National Natural Science Foundation of China(81425013 ; 91332113 ; 81271551 ; 81401379 ; 81301201 ; 81601476 ; 81301202)
内容类型期刊论文
源URL[http://ir.ia.ac.cn/handle/173211/20325]  
专题自动化研究所_脑网络组研究中心
作者单位1.Tianjin Med Univ Gen Hosp, Dept Radiol, 154 Anshan Rd, Tianjin 300052, Peoples R China
2.Tianjin Med Univ Gen Hosp, Tianjin Key Lab Funct Imaging, 154 Anshan Rd, Tianjin 300052, Peoples R China
3.Chinese Acad Sci, Inst Automat, Brainnetome Ctr, Beijing, Peoples R China
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Shen, Junlin,Qin, Wen,Xu, Qiang,et al. Modulation of APOE and SORL1 genes on hippocampal functional connectivity in healthy young adults[J]. BRAIN STRUCTURE & FUNCTION,2017,222(6):2877-2889.
APA Shen, Junlin.,Qin, Wen.,Xu, Qiang.,Xu, Lixue.,Xu, Jiayuan.,...&Yu, Chunshui.(2017).Modulation of APOE and SORL1 genes on hippocampal functional connectivity in healthy young adults.BRAIN STRUCTURE & FUNCTION,222(6),2877-2889.
MLA Shen, Junlin,et al."Modulation of APOE and SORL1 genes on hippocampal functional connectivity in healthy young adults".BRAIN STRUCTURE & FUNCTION 222.6(2017):2877-2889.
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