The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease
Authors:
- Carmen AntúnezCACarmen Antúnez
- Mercè BoadaMBMercè Boada
- Antonio González-PérezAGAntonio González-Pérez
- Javier GayánJGJavier Gayán
- Reposo Ramírez-LorcaRRReposo Ramírez-Lorca
- Juan MarínJMJuan Marín
- Isabel HernándezIHIsabel Hernández
- Concha Moreno-ReyCMConcha Moreno-Rey
- Francisco Jesús MorónFMFrancisco Jesús Morón
- Jesús López-ArrietaJLJesús López-Arrieta
- Ana MauleónAMAna Mauleón
- Maitée Rosende-RocaMRMaitée Rosende-Roca
Open Access
- 31 May 2011
- journal article
- Published by Springer Nature in Genome Medicine
- Vol. 3 (5) , 33
Abstract
Background: In order to identify novel loci associated with Alzheimer's disease (AD), we conducted a genome-wide association study (GWAS) in the Spanish population. Methods: We genotyped 1,128 individuals using the Affymetrix Nsp I 250K chip. A sample of 327 sporadic AD patients and 801 controls with unknown cognitive status from the Spanish general population were included in our initial study. To increase the power of the study, we combined our results with those of four other public GWAS datasets by applying identical quality control filters and the same imputation methods, which were then analyzed with a global meta-GWAS. A replication sample with 2,200 sporadic AD patients and 2,301 controls was genotyped to confirm our GWAS findings. Results: Meta-analysis of our data and independent replication datasets allowed us to confirm a novel genome-wide significant association of AD with the membrane-spanning 4-domains subfamily A (MS4A) gene cluster (rs1562990, P = 4.40E-11, odds ratio = 0.88, 95% confidence interval 0.85 to 0.91, n = 10,181 cases and 14,341 controls). Conclusions: Our results underscore the importance of international efforts combining GWAS datasets to isolate genetic loci for complex diseases.Keywords
This publication has 30 references indexed in Scilit:
- Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's diseaseNature Genetics, 2011
- Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's diseaseNature Genetics, 2011
- MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypesGenetic Epidemiology, 2010
- Genome-wide Analysis of Genetic Loci Associated With Alzheimer DiseaseJAMA, 2010
- Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's diseaseNature Genetics, 2009
- PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage AnalysesThe American Journal of Human Genetics, 2007
- GAB2 Alleles Modify Alzheimer's Risk in APOE ɛ4 CarriersNeuron, 2007
- Principal components analysis corrects for stratification in genome-wide association studiesNature Genetics, 2006
- The Human Genome Browser at UCSCGenome Research, 2002
- Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's diseaseNature, 1991