The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease

Carmen Antúnez(Nexen (Canada)), Merçé Boada(Universitat Autònoma de Barcelona), Antonio González‐Pérez, Javier Gayán, Reposo Ramírez‐Lorca, Juan Marín(Hospital Universitario Virgen de la Arrixaca), Isabel Hernández(Fundació ACE), Concha Moreno‐Rey, Francisco Jesús Morón, Jesús López‐Arrieta(Hospital Universitario La Paz), Ana Mauleón(Fundació ACE), Maitée Rosende‐Roca(Fundació ACE), Fuensanta Noguera-Perea(Hospital Universitario Virgen de la Arrixaca), Agustina Legaz-García(Hospital Universitario Virgen de la Arrixaca), L. Vivancos(Hospital Universitario Virgen de la Arrixaca), Juan Velasco, José Miguel Carrasco, Montserrat Alegret(Fundació ACE), Martirio Antequera-Torres(Hospital Universitario Virgen de la Arrixaca), Salvadora Manzanares(Hospital Universitario Virgen de la Arrixaca), Alejandro Romo, Irene Blanca, Susana Ruiz(Fundació ACE), Ana Espinosa(Fundació ACE), Sandra Castaño(Hospital Universitario Virgen de la Arrixaca), Blanca García García(Hospital Universitario Virgen de la Arrixaca), B. Martínez(Hospital Universitario Virgen de la Arrixaca), Georgina Vinyes(Fundació ACE), Asunción Lafuente(Fundació ACE), James T. Becker(University of Pittsburgh), José Jorge Galán, Manuel Serrano‐Ríos(Hospital Clínico San Carlos), Alzheimer's Disease Neuroimaging Initiative, Enrique Vázquez(Fundació ACE), Lluís Tárraga(Fundació ACE), María Eugenia Sáez(University of Pittsburgh), Oscar L. López(University of Pittsburgh), Luís Miguel Real, Agustı́n Ruiz
Genome Medicine
May 31, 2011
Cited by 102Open Access
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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.


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