No abstract

The prognosis and treatment of patients suffering from Alzheimer’s disease (AD) have been among the most important and challenging problems over the last few decades. To better understand the mechanism of AD, it is of great interest to identify genetic variants associated with brain atrophy. Commonly, in these analyses, neuroimaging features are extracted based on one of many possible brain atlases with FreeSurf and other popular software; this, however, may cause the loss of important information due to our incomplete knowledge about brain function embedded in these suboptimal atlases. To address the issue, we propose convolutional neural network (CNN) models applied to three-dimensional MRI data for the whole brain or multiple, divided brain regions to perform completely data-driven and automatic feature extraction. These image-derived features are then used as endophenotypes in genome-wide association studies (GWASs) to identify associated genetic variants. When we applied this method to ADNI data, we identified several associated SNPs that have been previously shown to be related to several neurodegenerative/mental disorders, such as AD, depression, and schizophrenia.

The prognosis and treatment of the patients suffering from Alzheimer's disease (AD) have been one of the most important and challenging problems over the last few decades. To better understand the mechanism of AD, it is of great interest to identify genetic variants associated with brain atrophy. Commonly in these analyses, neuroimaging features are extracted based on one of many possible brain atlases with FreeSurf and other popular softwares, which however may lose important information due to our incomplete knowledge about brain function embedded in these suboptimal atlases. To address the issue, we propose convolutional neural network (CNN) models applied to three-dimensional MRI data for the whole brain or multiple divided brain regions to perform completely data-driven and automatic feature extraction. These image-derived features are then used as endophenotypes in Genome-Wide Association Studies (GWAS) to identify associated genetic variants. When applied to the ADNI data, we identified several associated SNPs which have been previously shown to be related to several neurodegenerative/mental disorders such as AD, depression and schizophrenia. Code and supplementary materials are available at https://github.com/Dipnil07. The codes have been implemented using Python, R and Plink softwares.