Identification of novel genes for age‐at‐onset of Alzheimer's disease by combining quantitative and survival trait analyses

Author:

Li Yi‐Ju12,Nuytemans Karen34,La Jong ok2,Jiang Rong25,Slifer Susan H.4,Sun Shuming2,Naj Adam6,Gao Xiaoyi Raymond78,Martin Eden R.34

Affiliation:

1. Department of Biostatistics and Bioinformatics Duke University School of Medicine Durham North Carolina USA

2. Duke Molecular Physiology Institute Duke University School of Medicine Durham North Carolina USA

3. John P. Hussman Institute for Human Genomics University of Miami Miller School of Medicine Miami Florida USA

4. John T. MacDonald Foundation Department of Human Genetics University of Miami, Miller School of Medicine Miami Florida USA

5. Department of Psychiatry and Behavior Science Duke University School of Medicine Durham North Carolina USA

6. Department of Biostatistics Epidemiology, and Informatics Department of Pathology and Laboratory Medicine University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania USA

7. Department of Ophthalmology and Visual Sciences Division of Human Genetics The Ohio State University Columbus Ohio USA

8. Department of Biomedical Informatics The Ohio State University Columbus Ohio USA

Abstract

AbstractIntroductionOur understanding of the genetic predisposition for age‐at‐onset (AAO) of Alzheimer's disease (AD) is limited. Here, we sought to identify genes modifying AAO and examined whether any have sex‐specific effects.MethodsGenome‐wide association analysis were performed on imputed genetic data of 9219 AD cases and 10,345 controls from 20 cohorts of the Alzheimer's Disease Genetics Consortium. AAO was modeled from cases directly and as a survival outcome.ResultsWe identified 11 genome‐wide significant loci (P < 5 × 10−8), including six known AD‐risk genes and five novel loci, UMAD1, LUZP2, ARFGEF2, DSCAM, and 4q25, affecting AAO of AD. Additionally, 39 suggestive loci showed strong association. Twelve loci showed sex‐specific effects on AAO including CD300LG and MLX/TUBG2 for females and MIR4445 for males.DiscussionGenes that influence AAO of AD are excellent therapeutic targets for delaying onset of AD. Several loci identified include genes with promising functional implications for AD.

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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