Integrating brain imaging endophenotypes with GWAS for Alzheimer’s disease  

作　　者：Katherine AKnutson Wei Pan 

机构地区：[1]Division of Biostatistics,University of Minnesota,Minneapolis,MN 55455,USA

出　　处：《Quantitative Biology》2021年第2期185-200,共16页定量生物学（英文版）

基　　金：NIH grants T32GM108557,R01AG065636,R01HL116720,R01GM113250 and R01GM126002;by the Minnesota Supercomputing Institute at the University of Minnesota.

摘　　要：Background:Genome wide association studies(GWAS)have identified many genetic variants associated with increased risk of Alzheimer^disease(AD).These susceptibility loci may effect AD indirectly through a combination of physiological brain changes.Many of these neuropathologic features are detectable via magnetic resonance imaging(MRI).Methods:In this study,we examine the effects of such brain imaging derived phenotypes(IDPs)with genetic etiology on AD,using and comparing the following methods:two-sample Mendelian randomization(2SMR),generalized summary statistics based Mendelian randomization(GSMR),transcriptome wide association studies(TWAS)and the adaptive sum of powered score(aSPU)test.These methods do not require individual-level genotypic and phenotypic data but instead can rely only on an external reference panel and GWAS summary statistics.Results:Using publicly available GWAS datasets from the International Genomics of Alzheimer's Project(IGAP)and UK Biobank's(UKBB)brain imaging initiatives,we identify 35 IDPs possibly associated with AD,many of which have well established or biologically plausible links to the characteristic cognitive impairments of this neurodegenerative disease.Conclusions:Our results highlight the increased power for detecting genetic associations achieved by multiple correlated SNP-based methods,i.e.,aSPU,GSMR and TWAS,over MR methods based on independent SNPs(as instrumental variables).

关 键 词：aSPU test Mendelian randomization MRI SPU tests Sum test TWAS 

分 类 号：R749.16[医药卫生—神经病学与精神病学]