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Gene-Based Analysis in HRC Imputed Genome Wide Association Data Identifies Three Novel Genes For Alzheimer’s Disease

Baker, Emily; Sims, Rebecca; Leonenko, Ganna; Frizzati, Aura; Harwood, Janet; Grozeva, Detelina; Genetic and Environmental Risk in Alzheimer's Disease (GERAD) Consortium; PERADES consortium; IGAP consortia; Morgan, Kevin; Passmore, Peter; Holmes, Clive; Powell, John; Brayne, Carol; Gill, Michael; Mead, Simon; Heun, Reiner; Bossù, Paola; Spalletta, Gianfranco; Goate, Alison; Cruchaga, Carlos; van Duijn, Cornelia; Maier, Wolfgang; Ramirez, Alfredo; Jones, Lesley; Hardy, John; Ivanov, Dobril; Hill, Matthew; Holmans, Peter; Allen, Nicholas; Morgan, Paul; GERAD/PERADES; Williams, Julie; Escott-Price, Valentina; GERAD Consortium; ADGC Consortium; CHARGE Consortium; EADI Consortium

Authors

Emily Baker

Rebecca Sims

Ganna Leonenko

Aura Frizzati

Janet Harwood

Detelina Grozeva

Genetic and Environmental Risk in Alzheimer's Disease (GERAD) Consortium

PERADES consortium

IGAP consortia

Kevin Morgan

Peter Passmore

Clive Holmes

John Powell

Carol Brayne

Michael Gill

Simon Mead

Reiner Heun

Paola Bossù

Gianfranco Spalletta

Alison Goate

Carlos Cruchaga

Cornelia van Duijn

Wolfgang Maier

Alfredo Ramirez

Lesley Jones

John Hardy

Dobril Ivanov

Matthew Hill

Peter Holmans

Nicholas Allen

Paul Morgan

GERAD/PERADES

Julie Williams

Valentina Escott-Price

GERAD Consortium

ADGC Consortium

CHARGE Consortium

EADI Consortium



Abstract

A novel POLARIS gene-based analysis approach was employed to compute gene-based polygenic risk score (PRS) for all individuals in the latest HRC imputed GERAD (N cases=3332 and N controls=9,832) data using the International Genomics of Alzheimer's Project summary statistics (N cases=13676 and N controls= 27322, excluding GERAD subjects) to identify the SNPs and weight their risk alleles for the PRS score. SNPs were assigned to known, protein coding genes using GENCODE (v19). SNPs are assigned using both 1) no window around the gene and 2) a window of 35kb upstream and 10kb downstream to include transcriptional regulatory elements. The overall association of a gene is determined using a logistic regression model, adjusting for population covariates. Three novel gene wide significant genes were determined for the POLARIS gene-based analysis using a gene window; PPARGC1A, RORA and ZNF423. The ZNF432 gene resides in an Alzheimer's disease (AD) specific protein network which also includes other AD-related genes. The PPARGC1A gene has been linked to energy metabolism and the generation of amyloid beta plaques and the RORA has strong links with genes which are differentially expressed in the hippocampus. We also demonstrate no enrichment for genes in either loss of function intolerant or conserved noncoding sequence regions.

Citation

Baker, E., Sims, R., Leonenko, G., Frizzati, A., Harwood, J., Grozeva, D., Genetic and Environmental Risk in Alzheimer's Disease (GERAD) Consortium, PERADES consortium, IGAP consortia, Morgan, K., Passmore, P., Holmes, C., Powell, J., Brayne, C., Gill, M., Mead, S., Heun, R., Bossù, P., Spalletta, G., Goate, A., …EADI Consortium. Gene-Based Analysis in HRC Imputed Genome Wide Association Data Identifies Three Novel Genes For Alzheimer’s Disease

Working Paper Type Working Paper
Deposit Date Sep 6, 2018
Publicly Available Date Sep 6, 2018
Public URL https://nottingham-repository.worktribe.com/output/1062489
Publisher URL https://www.biorxiv.org/content/10.1101/374876v1
Additional Information This is a bioRxiv preprint.

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