作者
Yiyi Ma,Dolly Reyes‐Dumeyer,Angel Piriz,Patricia Recio,Diones Rivera Mejía,Martin Medrano,Rafael Lantigua,Jean Paul Vonsattel,Giuseppe Tosto,Andrew F. Teich,Benjamin Ciener,Sandra Leskinen,Sharanya Sivakumar,Michael DeTure,Duara Ranjan,Dennis W. Dickson,Melissa E. Murray,Edward B. Lee,David A. Wolk,Lee‐Way Jin,Brittany N. Dugger,Annie Hiniker,Robert A. Rissman,Richard Mayeux,Badri N. Vardarajan
摘要
Genetic variants and epigenetic features both contribute to the risk of Alzheimer's disease (AD). We studied the AD association of CpG-related single nucleotide polymorphisms (CGS), which act as a hub of both the genetic and epigenetic effects, in Caribbean Hispanics (CH) and generalized the findings to Non-Hispanic Whites (NHW). First, we conducted a genome-wide, sliding-window-based association with AD, in 7,155 CH and 1,283 NHW participants. Next, using data from the dorsolateral prefrontal cortex in 179 CH brains, we tested the cis- and trans-effects of AD-associated CGS on brain DNA methylation to mRNA expression. For the genes with significant cis- and trans-effects, we investigated their enriched pathways. We identified six genetic loci in CH with CGS dosage associated with AD at genome-wide significance levels: ADAM20 (Score = 55.19, P = 4.06 × 10