Identification of Novel Genes Associated with Cortical Thickness in Alzheimer's Disease: Systems Biology Approach to Neuroimaging Endophenotype

• Published in: Journal of Alzheimer's disease Vol. 75; no. 2; p. 531
• Main Authors: Kim, Bo-Hyun, Choi, Yong-Ho, Yang, Jin-Ju, Kim, SangYun, Nho, Kwangsik, Lee, Jong-Min
• Format: Journal Article
• Language: English
• Published: Netherlands 01.01.2020
• Subjects: Aged; Aged, 80 and over; Alzheimer Disease - diagnostic imaging; Alzheimer Disease - genetics; Brain Cortical Thickness; Disease Progression; Endophenotypes; Female; Genetic Markers; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Male; Neuroimaging; Polymorphism, Single Nucleotide; Quantitative Trait Loci; RNA, Long Noncoding - genetics; gene-based association analysis; Alzheimer’s disease; imaging genetics; brain; cortical thickness; genome-wide association study
• ISSN: 1875-8908
• DOI: 10.3233/JAD-191175

Alzheimer's disease (AD) is a common neurodegenerative disorder characterized by a heterogeneous distribution of pathological changes in the brain. Cortical thickness is one of the most sensitive imaging biomarkers for AD representing structural atrophy. The purpose of this study is to identify novel genes associated with cortical thickness. We measured the whole-brain mean cortical thickness from magnetic resonance imaging (MRI) scans in 919 subjects from the Alzheimer's Disease Neuroimaging Initiative cohort, including 163 AD patients, 488 mild cognitive impairment patients, and 268 cognitively normal participants. Based on the single-nucleotide polymorphism (SNP)-based genome-wide association study, we performed gene-based association analysis for mean cortical thickness. Furthermore, we performed expression quantitative trait loci, protein-protein interaction network, and pathway analysis to identify biologically functional information. We identified four genes (B4GALNT1, RAB44, LOC101927583, and SLC26A10), two pathways (cyclin-dependent protein kinase holoenzyme complex and nuclear cyclin-dependent protein kinase holoenzyme complex), and one protein-protein interaction (B4GALNT1 and GALNT8 pair). These genes are involved in protein degradation, GTPase activity, neuronal loss, and apoptosis. The identified pathways are involved in the cellular processes and neuronal differentiation, which contribute to neuronal loss that is responsible for AD. Furthermore, the most significant SNP (rs12320537) in B4GALNT1 is associated with expression levels of B4GALNT1 in several brain regions. Thus, the identified genes and pathways provide deeper mechanistic insight into the molecular basis of brain atrophy in AD.