Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.

  • Denise Harold
  • Richard Abraham
  • Paul Hollingworth
  • Rebecca Sims
  • Amy Gerrish
  • Marian L Hamshere
  • Jaspreet Singh Pahwa
  • Valentina Moskvina
  • Kimberley Dowzell
  • Amy Williams
  • Nicola Jones
  • Charlene Thomas
  • Alexandra Stretton
  • Angharad R Morgan
  • Simon Lovestone
  • John Powell
  • Petroula Proitsi
  • Michelle K Lupton
  • Carol Brayne
  • David C Rubinsztein
  • Michael Gill
  • Brian Lawlor
  • Aoibhinn Lynch
  • Kevin Morgan
  • Kristelle S Brown
  • Peter A Passmore
  • David Craig
  • Bernadette McGuinness
  • Stephen Todd
  • Clive Holmes
  • David Mann
  • A David Smith
  • Seth Love
  • Patrick G Kehoe
  • John Hardy
  • Simon Mead
  • Nick Fox
  • Martin Rossor
  • John Collinge
  • Wolfgang Maier
  • Frank Jessen
  • Britta Schürmann
  • Hendrik Bussche van den
  • Isabella Heuser
  • Johannes Kornhuber
  • Jens Wiltfang
  • Martin Dichgans
  • Lutz Frölich
  • Harald Hampel
  • Michael Hüll
  • Dan Rujescu
  • Alison M Goate
  • John S K Kauwe
  • Carlos Cruchaga
  • Petra Nowotny
  • John C Morris
  • Kevin Mayo
  • Kristel Sleegers
  • Karolien Bettens
  • Sebastiaan Engelborghs
  • De Deyn
  • P Peter
  • Van Broeckhoven Christine
  • Gill Livingston
  • Nicholas J Bass
  • Hugh Gurling
  • Andrew McQuillin
  • Rhian Gwilliam
  • Panagiotis Deloukas
  • Ammar Al-Chalabi
  • Christopher E Shaw
  • Magda Tsolaki
  • Andrew B Singleton
  • Rita Guerreiro
  • Thomas W Mühleisen
  • Markus M Nöthen
  • Susanne Moebus
  • Karl-Heinz Jöckel
  • Norman Klopp
  • H-Erich Wichmann
  • Minerva M Carrasquillo
  • V Shane Pankratz
  • Steven G Younkin
  • Peter A Holmans
  • O'Donovan Michael
  • Michael J Owen
  • Julie Williams

Abstract

We undertook a two-stage genome-wide association study (GWAS) of Alzheimer's disease (AD) involving over 16,000 individuals, the most powerful AD GWAS to date. In stage 1 (3,941 cases and 7,848 controls), we replicated the established association with the apolipoprotein E (APOE) locus (most significant SNP, rs2075650, P = 1.8 x 10(-157)) and observed genome-wide significant association with SNPs at two loci not previously associated with the disease: at the CLU (also known as APOJ) gene (rs11136000, P = 1.4 x 10(-9)) and 5' to the PICALM gene (rs3851179, P = 1.9 x 10(-8)). These associations were replicated in stage 2 (2,023 cases and 2,340 controls), producing compelling evidence for association with Alzheimer's disease in the combined dataset (rs11136000, P = 8.5 x 10(-10), odds ratio = 0.86; rs3851179, P = 1.3 x 10(-9), odds ratio = 0.86).

Bibliographical data

Original languageGerman
Article number10
ISSN1061-4036
Publication statusPublished - 2009
pubmed 19734902