Integrating Transcriptomics, Genomics, and Imaging in Alzheimer’s Disease: A Federated Model

Author:

Wu JianfengORCID,Chen Yanxi,Wang Panwen,Caselli Richard J,Thompson Paul M,Wang Junwen,Wang YalinORCID,

Abstract

AbstractAlzheimer’s disease (AD) affects more than 1 in 9 people age 65 and older and becomes an urgent public health concern as the global population ages. In clinical practice, structural magnetic resonance imaging (sMRI) is the most accessible and widely used diagnostic imaging modality. Additionally, genome-wide association studies (GWAS) and transcriptomics – the study of gene expression – also play an important role in understanding AD etiology and progression. Sophisticated imaging genetics systems have been developed to discover genetic factors that consistently affect brain function and structure. However, most studies to date focused on the relationships between brain sMRI and GWAS or brain sMRI and transcriptomics. To our knowledge, few methods have been developed to discover and infer multimodal relationships among sMRI, GWAS, and transcriptomics. To address this, we propose a novel federated model, Genotype-Expression-Imaging Data Integration (GEIDI), to identify genetic and transcriptomic influences on brain sMRI measures. The relationships between brain imaging measures and gene expression are allowed to depend on a person’s genotype at the single-nucleotide polymorphism (SNP) level, making the inferences adaptive and personalized. We performed extensive experiments on publicly available Alzheimer’s Disease Neuroimaging Initiative (ADNI) dataset. Experimental results demonstrated our proposed method outperformed state-of-the-art expression quantitative trait loci (eQTL) methods for detecting genetic and transcriptomic factors related to AD and has stable performance when data are integrated from multiple sites. Our GEIDI approach may offer novel insights into the relationship among image biomarkers, genotypes, and gene expression and help discover novel genetic targets for potential AD drug treatments.

Publisher

Cold Spring Harbor Laboratory

Reference67 articles.

1. Albert, F.W. , Kruglyak, L. , 2015. The role of regulatory variation in complex traits and disease. Nat. Rev. Genet. https://doi.org/10.1038/nrg3891

2. Barbur, V.A. , Montgomery, D.C. , Peck, E.A. , 1994. Introduction to Linear Regression Analysis. Stat. 43. https://doi.org/10.2307/2348362

3. Plasma Biomarkers of AD Emerging as Essential Tools for Drug Development: An EU/US CTAD Task Force Report;J. Prev. Alzheimer’s Dis,2019

4. Berkopec, A. , 2007. HyperQuick algorithm for discrete hypergeometric distribution. J. Discret. Algorithms. https://doi.org/10.1016/j.jda.2006.01.001

5. Bis, J.C. , Jian, X. , Kunkle, B.W. , Chen, Y. , Hamilton-Nelson, K.L. , Bush, W.S. , Salerno, W.J. , Lancour, D. , Ma, Y. , Renton, A.E. , Marcora, E. , Farrell, J.J. , Zhao, Y. , Qu, L. , Ahmad, S. , Amin, N. , Amouyel, P. , Beecham, G.W. , Below, J.E. , Campion, D. , Cantwell, L. , Charbonnier, C. , Chung, J. , Crane, P.K. , Cruchaga, C. , Cupples, L.A. , Dartigues, J.F. , Debette, S. , Deleuze, J.F. , Fulton, L. , Gabriel, S.B. , Genin, E. , Gibbs, R.A. , Goate, A. , Grenier-Boley, B. , Gupta, N. , Haines, J.L. , Havulinna, A.S. , Helisalmi, S. , Hiltunen, M. , Howrigan, D.P. , Ikram, M.A. , Kaprio, J. , Konrad, J. , Kuzma, A. , Lander, E.S. , Lathrop, M. , Lehtimäki, T. , Lin, H. , Mattila, K. , Mayeux, R. , Muzny, D.M. , Nasser, W. , Neale, B. , Nho, K. , Nicolas, G. , Patel, D. , Pericak-Vance, M.A. , Perola, M. , Psaty, B.M. , Quenez, O. , Rajabli, F. , Redon, R. , Reitz, C. , Remes, A.M. , Salomaa, V. , Sarnowski, C. , Schmidt, H. , Schmidt, M. , Schmidt, R. , Soininen, H. , Thornton, T.A. , Tosto, G. , Tzourio, C. , van der Lee, S.J. , van Duijn, C.M. , Valladares, O. , Vardarajan, B. , Wang, L.S. , Wang, W. , Wijsman, E. , Wilson, R.K. , Witten, D. , Worley, K.C. , Zhang, X. , Bellenguez, C. , Lambert, J.C. , Kurki, M.I. , Palotie, A. , Daly, M. , Boerwinkle, E. , Lunetta, K.L. , Destefano, A.L. , Dupuis, J. , Martin, E.R. , Schellenberg, G.D. , Seshadri, S. , Naj, A.C. , Fornage, M. , Farrer, L.A. , 2020. Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation. Mol. Psychiatry. https://doi.org/10.1038/s41380-018-0112-7

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