The application of deep learning techniques to the detection and automated classification of Alzheimer's disease (AD) has recently gained considerable attention. The rapid progress in neuroimaging and sequencing techniques has enabled the generation of large-scale imaging genetic data for AD research. In this study, we developed a deep learning approach, IGnet, for automated AD classification using both magnetic resonance imaging (MRI) data and genetic sequencing data. The proposed approach integrates computer vision (CV) and natural language processing (NLP) techniques, with a deep three-dimensional convolutional network (3D CNN) being used to handle the three-dimensional MRI input and a Transformer encoder being used to manage the genetic sequence input. The proposed approach has been applied to the Alzheimer's Disease Neuroimaging Initiative (ADNI) data set. Using baseline MRI scans and selected single-nucleotide polymorphisms on chromosome 19, it achieved a classification accuracy of 83.78% and an area under the receiver operating characteristic curve (AUC-ROC) of 0.924 with the test set. The results demonstrate the great potential of using multi-disciplinary AI approaches to integrate imaging genetic data for the automated classification of AD.

Tobacco smoking is an addictive behavior that supports nicotine dependence and is an independent risk factor for cancer and other illnesses. Its neurogenetic mechanisms are not fully understood but may act through alterations in the cerebral white matter (WM). We hypothesized that the vertical pleiotropic pathways, where genetic variants influence a trait that in turn influences another trait, link genetic factors, integrity of cerebral WM, and nicotine addiction. We tested this hypothesis using individual genetic factors, WM integrity measured by fractional anisotropy (FA), and nicotine dependence-related smoking phenotypes, including smoking status (SS) and cigarettes per day (CPDs), in a large epidemiological sample collected by the UK Biobank. We performed a genome-wide association study (GWAS) to identify previously reported loci associated with smoking behavior. Smoking was found to be associated with reduced WM integrity in multiple brain regions. We then evaluated two competing vertical pathways: Genes → WM integrity → Smoking versus Genes → Smoking → WM integrity and a horizontal pleiotropy pathway where genetic factors independently affect both smoking and WM integrity. The causal pathway analysis identified 272 pleiotropic single-nucleotide polymorphisms (SNPs) whose effects on SS were mediated by FA, as well as 22 pleiotropic SNPs whose effects on FA were mediated by CPD. These SNPs were mainly located in important susceptibility genes for smoking-induced diseases NCAM1 and IREB2. Our findings revealed the role of cerebral WM in the maintenance of the complex addiction and provided potential genetic targets for future research in examining how changes in WM integrity contribute to the nicotine effects on the brain.