Title
Genetics of cognitive trajectory in Brazilians: 15 years of follow-up from the Bambuí-Epigen Cohort Study of Aging
Date Issued
01 December 2019
Access level
open access
Resource Type
journal article
Author(s)
Gouveia M.H.
Cesar C.C.
Anna H.P.S.
Scliar M.O.
Leal T.P.
Araújo N.M.
Soares-Souza G.B.
Magalhães W.C.S.
Mata I.F.
Ferri C.P.
Castro-Costa E.
Mbulaiteye S.M.
Tishkoff S.A.
Shriner D.
Rotimi C.N.
Lima-Costa M.F.
Universidade Federal de Minas Gerais
Universidade Federal de Minas Gerais
Publisher(s)
Nature Research
Abstract
Age-related cognitive decline (ACD) is the gradual process of decreasing of cognitive function over age. Most genetic risk factors for ACD have been identified in European populations and there are no reports in admixed Latin American individuals. We performed admixture mapping, genome-wide association analysis (GWAS), and fine-mapping to examine genetic factors associated with 15-year cognitive trajectory in 1,407 Brazilian older adults, comprising 14,956 Mini-Mental State Examination measures. Participants were enrolled as part of the Bambuí-Epigen Cohort Study of Aging. Our admixture mapping analysis identified a genomic region (3p24.2) in which increased Native American ancestry was significantly associated with faster ACD. Fine-mapping of this region identified a single nucleotide polymorphism (SNP) rs142380904 (β = −0.044, SE = 0.01, p = 7.5 × 10−5) associated with ACD. In addition, our GWAS identified 24 associated SNPs, most in genes previously reported to influence cognitive function. The top six associated SNPs accounted for 18.5% of the ACD variance in our data. Furthermore, our longitudinal study replicated previous GWAS hits for cognitive decline and Alzheimer’s disease. Our 15-year longitudinal study identified both ancestry-specific and cosmopolitan genetic variants associated with ACD in Brazilians, highlighting the need for more trans-ancestry genomic studies, especially in underrepresented ethnic groups.
Volume
9
Issue
1
Language
English
OCDE Knowledge area
Genética humana
Scopus EID
2-s2.0-85075918104
PubMed ID
Source
Scientific Reports
Sponsor(s)
We thank Victor Borda for scientific discussions. The EPIGEN-Brazil Initiative is funded by the Brazilian Ministry of Health (Department of Science and Technology from the Secretaria de Ciência, Tecnologia e Insumos Estratégicos) through Financiadora de Estudos e Projetos. The EPIGEN-Brazil investigators received funding from the Brazilian Ministry of Education (CAPES Agency). MHG, MLS, MFLC, ETS and TPL were supported by Brazilian National Research Council (CNPq), Minas Gerais Research Agency (FAPEMIG) and Pró-Reitoria de Pesquisa da Universidade Federal de Minas Gerais. Tishkoff laboratory is funded by the National Institutes of Health (1R01DK104339-0 and 1R01GM113657-01). MHG is supported by the Intramural Research Program of the National Institutes of Health in the Center for Research on Genomics and Global Health (CRGGH). The CRGGH is supported by the National Human Genome Research Institute, the National Institute of Diabetes and Digestive and Kidney Diseases, the Center for Information Technology, and the Office of the Director at the National Institutes of Health (1ZIAHG200362).
Sources of information: Directorio de Producción Científica Scopus